| Year |
Citation |
Score |
| 2021 |
Porth S, Bats JW, Trauner D, Giester G, Mulzer J. Insight into the Mechanism of the Saegusa Oxidation: Isolation of a Novel Palladium(0)-Tetraolefin Complex. Angewandte Chemie (International Ed. in English). 38: 2015-2016. PMID 34182691 DOI: 10.1002/(SICI)1521-3773(19990712)38:13/14<2015::AID-ANIE2015>3.0.CO;2-# |
0.364 |
|
| 2016 |
Farcet J, Mulzer J, Himmelbauer MK. An Approach Toward the Bridged 14‐Membered Carbon Macrocycle of Bielschowskysin European Journal of Organic Chemistry. 2016: 2793-2801. DOI: 10.1002/Ejoc.201600271 |
0.421 |
|
| 2015 |
Aichinger C, Mulzer J, Rinner U. Synthesis of the C6-C14 Fragment of Euphosalicin Synlett. 26: 1852-1856. DOI: 10.1055/S-0034-1380422 |
0.731 |
|
| 2014 |
Preindl J, Leitner C, Baldauf S, Mulzer J. A short access to the skeleton of Elisabethin A and formal syntheses of Elisapterosin B and Colombiasin A. Organic Letters. 16: 4276-9. PMID 25089586 DOI: 10.1021/Ol501998Y |
0.451 |
|
| 2014 |
Toelle N, Weinstabl H, Gaich T, Mulzer J. Light-mediated total synthesis of 17-deoxyprovidencin. Angewandte Chemie (International Ed. in English). 53: 3859-62. PMID 24604885 DOI: 10.1002/Anie.201400617 |
0.437 |
|
| 2014 |
Mulzer J. Trying to rationalize total synthesis. Natural Product Reports. 31: 595-603. PMID 24589568 DOI: 10.1039/C3Np70105K |
0.373 |
|
| 2014 |
Lentsch C, Fürst R, Mulzer J, Rinner U. Jatrophane diterpenes: Preparation of the western fragment of pl-3 European Journal of Organic Chemistry. 2014: 919-923. DOI: 10.1002/Ejoc.201301616 |
0.721 |
|
| 2013 |
Siengalewicz P, Mulzer J, Rinner U. Lycopodium alkaloids--synthetic highlights and recent developments. The Alkaloids. Chemistry and Biology. 72: 1-151. PMID 24712098 DOI: 10.1016/B978-0-12-407774-4.00001-7 |
0.688 |
|
| 2013 |
Himmelbauer M, Farcet JB, Gagnepain J, Mulzer J. A palladium-catalyzed carbo-oxygenation: the bielschowskysin case. Organic Letters. 15: 3098-101. PMID 23724910 DOI: 10.1021/Ol401285D |
0.373 |
|
| 2013 |
Farcet JB, Himmelbauer M, Mulzer J. An approach to the carbon backbone of bielschowskysin, part 2: Non-photochemical strategy European Journal of Organic Chemistry. 8245-8252. DOI: 10.1002/Ejoc.201300870 |
0.356 |
|
| 2013 |
Himmelbauer M, Farcet JB, Gagnepain J, Mulzer J. An approach to the carbon backbone of bielschowskysin, part 1: Photocyclization strategy European Journal of Organic Chemistry. 8214-8244. DOI: 10.1002/Ejoc.201300869 |
0.372 |
|
| 2013 |
Farcet JB, Himmelbauer M, Mulzer J. Photochemical and thermal [2 + 2] cycloaddition to generate the bicyclo[3.2.0]heptane core of bielschowskysin European Journal of Organic Chemistry. 4379-4398. DOI: 10.1002/Ejoc.201300382 |
0.321 |
|
| 2012 |
Enev VS, Felzmann W, Gromov A, Marchart S, Mulzer J. Total synthesis of branimycin: an evolutionary approach. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 9651-68. PMID 22764044 DOI: 10.1002/Chem.201200257 |
0.444 |
|
| 2012 |
Weinstabl H, Gaich T, Mulzer J. Application of the Rodriguez-Pattenden photo-ring contraction: total synthesis and configurational reassignment of 11-gorgiacerol and 11-epigorgiacerol. Organic Letters. 14: 2834-7. PMID 22590980 DOI: 10.1021/Ol301068H |
0.47 |
|
| 2012 |
Farcet JB, Himmelbauer M, Mulzer J. A non-photochemical approach to the bicyclo[3.2.0]heptane core of bielschowskysin. Organic Letters. 14: 2195-7. PMID 22506798 DOI: 10.1021/Ol3006419 |
0.396 |
|
| 2012 |
Martin HJ, Magauer T, Mulzer J. In pursuit of an elusive target: Our kendomycin story Strategies and Tactics in Organic Synthesis. 8: 261-289. DOI: 10.1016/B978-0-12-386540-3.00010-1 |
0.703 |
|
| 2012 |
Ramharter J, Mulzer J. From planning to optimization: Total synthesis of valerenic acid and some bioactive derivatives European Journal of Organic Chemistry. 2041-2053. DOI: 10.1002/Ejoc.201101834 |
0.455 |
|
| 2011 |
Ramharter J, Mulzer J. Efficient and scalable one-pot synthesis of 2,4-dienols from cycloalkenones: optimized total synthesis of valerenic acid. Organic Letters. 13: 5310-3. PMID 21894886 DOI: 10.1021/Ol202170C |
0.391 |
|
| 2011 |
Ramharter J, Mulzer J. One-Pot Synthesis of 2,4-Dienols from Cycloalkenones Synfacts. 2011: 1350-1350. DOI: 10.1055/S-0031-1289358 |
0.465 |
|
| 2011 |
Ramharter J, Weinstabl H, Mulzer J. Synthesis of (+)-Lycoflexine Synfacts. 2011: 125-125. DOI: 10.1055/S-0030-1259218 |
0.457 |
|
| 2011 |
Sicking W, Sustmann R, Mulzer J, Huisgen R. The rearrangement of 2,2-diphenyl-1-[(E)-2-phenylethenyl]cyclopropane to 3,4,4-triphenylcyclopent-1-ene: A DFT analysis Helvetica Chimica Acta. 94: 1389-1405. DOI: 10.1002/Hlca.201100142 |
0.404 |
|
| 2011 |
Mulzer J, Huisgen R, Arion V, Sustmann R. 1-[(E)-2-arylethenyl]-2,2-diphenylcyclopropanes: Kinetics and mechanism of rearrangement to cyclopentenes Helvetica Chimica Acta. 94: 1359-1388. DOI: 10.1002/Hlca.201100135 |
0.47 |
|
| 2011 |
Siengalewicz P, Mulzer J, Rinner U. Synthesis of protoilludanes and related sesquiterpenes European Journal of Organic Chemistry. 7041-7055. DOI: 10.1002/Ejoc.201101220 |
0.701 |
|
| 2010 |
Ramharter J, Weinstabl H, Mulzer J. Synthesis of the lycopodium alkaloid (+)-lycoflexine. Journal of the American Chemical Society. 132: 14338-9. PMID 20866095 DOI: 10.1021/Ja107533M |
0.456 |
|
| 2010 |
Martin HJ, Magauer T, Mulzer J. In pursuit of a competitive target: total synthesis of the antibiotic kendomycin. Angewandte Chemie (International Ed. in English). 49: 5614-26. PMID 20818753 DOI: 10.1002/Anie.201000227 |
0.704 |
|
| 2010 |
Gaich T, Mulzer J. From silphinenes to penifulvins: a biomimetic approach to penifulvins B and C. Organic Letters. 12: 272-5. PMID 20000335 DOI: 10.1021/Ol902594B |
0.378 |
|
| 2010 |
Magauer T, Martin HJ, Mulzer J. Ring-closing metathesis and photo-fries reaction for the construction of the ansamycin antibiotic kendomycin: development of a protecting group free oxidative endgame. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 507-19. PMID 19950336 DOI: 10.1002/Chem.200902226 |
0.705 |
|
| 2010 |
Prantz K, Mulzer J. Synthesis of (Z)-trisubstituted olefins by decarboxylative grob-type fragmentations: epothilone D, discodermolide, and peloruside A. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 485-506. PMID 19943284 DOI: 10.1002/Chem.200901567 |
0.398 |
|
| 2010 |
Gromov A, Enev V, Mulzer J. Improved synthesis of parent fused 7-oxanorbornenes Synthetic Communications. 40: 104-110. DOI: 10.1080/00397910902953323 |
0.349 |
|
| 2010 |
Marchart S, Gromov A, Mulzer J. Synthesis of Branimycin Synfacts. 2010: 629-629. DOI: 10.1055/S-0029-1219855 |
0.457 |
|
| 2010 |
Magauer T, Mulzer J, Tiefenbacher K. Syntheses of (+)-Echinopine A and B Synfacts. 2010: 376-376. DOI: 10.1055/S-0029-1219451 |
0.625 |
|
| 2010 |
Magauer T, Martin HJ, Mulzer J. Synthesis of Kendomycin Synfacts. 2010: 17-17. DOI: 10.1055/S-0029-1218394 |
0.712 |
|
| 2010 |
Tiefenbacher K, Tröndlin L, Mulzer J, Pfaltz A. An expeditious asymmetric formal synthesis of the antibiotic platensimycin Tetrahedron. 66: 6508-6513. DOI: 10.1016/J.Tet.2010.04.098 |
0.364 |
|
| 2010 |
Magauer T, Martin H, Mulzer J. Inside Cover: Ring-Closing Metathesis and Photo-Fries Reaction for the Construction of the Ansamycin Antibiotic Kendomycin: Development of a Protecting Group Free Oxidative Endgame (Chem. Eur. J. 2/2010) Chemistry - a European Journal. 16: 384-384. DOI: 10.1002/Chem.200990203 |
0.654 |
|
| 2010 |
Martin H, Magauer T, Mulzer J. Einem kompetitiven Zielmolekül auf den Fersen: Totalsynthese des Antibiotikums Kendomycin Angewandte Chemie. 122: 5746-5758. DOI: 10.1002/Ange.201000227 |
0.609 |
|
| 2009 |
Magauer T, Mulzer J, Tiefenbacher K. Total syntheses of (+)-echinopine A and B: determination of absolute stereochemistry. Organic Letters. 11: 5306-9. PMID 19824621 DOI: 10.1021/Ol902263K |
0.682 |
|
| 2009 |
Gromov A, Enev V, Mulzer J. A desymmetrization approach toward highly oxygenated cis-decalins. Organic Letters. 11: 2884-6. PMID 19507868 DOI: 10.1021/Ol900834C |
0.343 |
|
| 2009 |
Prantz K, Mulzer J. Decarboxylative Grob-type fragmentations in the synthesis of trisubstituted Z olefins: application to peloruside A, discodermolide, and epothilone D. Angewandte Chemie (International Ed. in English). 48: 5030-3. PMID 19492384 DOI: 10.1002/Anie.200901740 |
0.372 |
|
| 2009 |
Gollner A, Altmann KH, Gertsch J, Mulzer J. The laulimalide family: total synthesis and biological evaluation of neolaulimalide, isolaulimalide, laulimalide and a nonnatural analogue. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 5979-97. PMID 19402092 DOI: 10.1002/Chem.200802605 |
0.406 |
|
| 2009 |
Magauer T, Martin HJ, Mulzer J. Total synthesis of the antibiotic kendomycin by macrocyclization using photo-Fries rearrangement and ring-closing metathesis. Angewandte Chemie (International Ed. in English). 48: 6032-6. PMID 19350596 DOI: 10.1002/Anie.200900522 |
0.7 |
|
| 2009 |
Tiefenbacher K, Mulzer J. A nine-step total synthesis of (-)-platencin. The Journal of Organic Chemistry. 74: 2937-41. PMID 19260660 DOI: 10.1021/Jo9001855 |
0.453 |
|
| 2009 |
Ramharter J, Mulzer J. Total synthesis of valerenic acid, a potent GABAA receptor modulator. Organic Letters. 11: 1151-3. PMID 19178294 DOI: 10.1021/Ol9000137 |
0.394 |
|
| 2009 |
Gaich T, Mulzer J. Total synthesis of (-)-Penifulvin A, an insecticide with a dioxafenestrane skeleton. Journal of the American Chemical Society. 131: 452-3. PMID 19140787 DOI: 10.1021/Ja8083048 |
0.423 |
|
| 2009 |
Innitzer A, Mulzer J. A tetracarbonyl Paal-Knorr approach to semicorrins Heterocycles. 77: 873-886. DOI: 10.3987/Com-08-S(F)54 |
0.364 |
|
| 2009 |
Ramharter J, Mulzer J. Synthesis of Valerenic Acid Synfacts. 2009: 1062-1062. DOI: 10.1055/S-0029-1217869 |
0.367 |
|
| 2009 |
Gaich T, Mulzer J. Synthesis of (-)-Penifulvin A Synfacts. 2009: 704-704. DOI: 10.1055/S-0029-1217244 |
0.457 |
|
| 2009 |
Gaich T, Weinstabl H, Mulzer J. Synthetic efforts towards the synthesis of the complex diterpene providencin Synlett. 1357-1366. DOI: 10.1055/S-0028-1216728 |
0.437 |
|
| 2009 |
Tiefenbacher K, Mulzer J. Formal Synthesis of (-)-Platencin Synfacts. 2009: 122-122. DOI: 10.1055/S-0028-1087606 |
0.453 |
|
| 2009 |
Gollner A, Altmann KH, Gertsch J, Mulzer J. Synthesis and biological evaluation of a des-dihydropyran laulimalide analog Tetrahedron Letters. 50: 5790-5792. DOI: 10.1016/J.Tetlet.2009.07.122 |
0.446 |
|
| 2009 |
Gromov A, Enev V, Mulzer J. Remarkable temperature effect on intramolecular [3+2] cyclization Tetrahedron Letters. 50: 5283-5284. DOI: 10.1016/J.Tetlet.2009.07.030 |
0.324 |
|
| 2009 |
Rinner U, Mulzer J. Elements of Synthesis Planning. By R. W. Hoffmann. Angewandte Chemie. 48: 9590-9591. DOI: 10.1002/Anie.200905457 |
0.664 |
|
| 2009 |
Prantz K, Mulzer J. Decarboxylierende Grob-Fragmentierung zur Synthese trisubstituierter Z-Olefine: Anwendung auf Pelorusid A, Discodermolid und Epothilon D† Angewandte Chemie. 121: 5130-5133. DOI: 10.1002/Ange.200901740 |
0.354 |
|
| 2009 |
Magauer T, Martin H, Mulzer J. Totalsynthese des Antibiotikums Kendomycin durch Photo-Fries-Umlagerung und Ringschlussmetathese Angewandte Chemie. 121: 6148-6152. DOI: 10.1002/Ange.200900522 |
0.592 |
|
| 2008 |
Siengalewicz P, Rinner U, Mulzer J. Recent progress in the total synthesis of naphthyridinomycin and lemonomycin tetrahydroisoquinoline antitumor antibiotics (TAAs). Chemical Society Reviews. 37: 2676-90. PMID 19020681 DOI: 10.1039/B804167A |
0.701 |
|
| 2008 |
Gollner A, Mulzer J. Total synthesis of neolaulimalide and isolaulimalide. Organic Letters. 10: 4701-4. PMID 18816129 DOI: 10.1021/Ol802075V |
0.447 |
|
| 2008 |
Siengalewicz P, Gaich T, Mulzer J. It all began with an error: the nomofungin/communesin story. Angewandte Chemie (International Ed. in English). 47: 8170-6. PMID 18814155 DOI: 10.1002/Anie.200801735 |
0.329 |
|
| 2008 |
Tiefenbacher K, Mulzer J. Short formal synthesis of (-)-platencin. Angewandte Chemie (International Ed. in English). 47: 6199-200. PMID 18600810 DOI: 10.1002/Anie.200801441 |
0.422 |
|
| 2008 |
Tiefenbacher K, Mulzer J. Synthesis of platensimycin. Angewandte Chemie (International Ed. in English). 47: 2548-55. PMID 18327757 DOI: 10.1002/Anie.200705303 |
0.317 |
|
| 2008 |
Enev VS, Drescher M, Mulzer J. A non-Diels-Alder approach to the cis-decalin core of branimycin. Organic Letters. 10: 413-6. PMID 18161981 DOI: 10.1021/Ol7027338 |
0.37 |
|
| 2008 |
Mulzer J, Drescher M, Enev VS. Quinic acid as versatile chiral scaffold in organic synthesis Current Organic Chemistry. 12: 1613-1630. DOI: 10.2174/138527208786786291 |
0.361 |
|
| 2008 |
Siengalewicz P, Brecker L, Mulzer J. Stereocontrolled synthesis of the tetracyclic core framework of (-)-lemonomycin Synlett. 2443-2446. DOI: 10.1055/S-2008-1078273 |
0.422 |
|
| 2008 |
Kögl M, Brecker L, Warrass R, Mulzer J. Synthesis of Pasteurestin A and B Synfacts. 2008: 446-446. DOI: 10.1055/S-2008-1072705 |
0.367 |
|
| 2008 |
Barth R, Mulzer J. Two-directional total synthesis of efomycine M and formal total synthesis of elaiolide Tetrahedron. 64: 4718-4735. DOI: 10.1016/J.Tet.2008.01.114 |
0.44 |
|
| 2008 |
Kögl M, Brecker L, Warrass R, Mulzer J. Novel protoilludane lead structure for veterinary antibiotics: Total synthesis of pasteurestins A and B and assignment of their configurations European Journal of Organic Chemistry. 2714-2730. DOI: 10.1002/Ejoc.200800074 |
0.398 |
|
| 2008 |
Rinner U, Mulzer J. The Way of Synthesis. Evolution of Design and Methods for Natural Products. Von Tomáš Hudlický und Josephine W. Reed. Angewandte Chemie. 120: 32-32. DOI: 10.1002/Ange.200785550 |
0.675 |
|
| 2008 |
Mulzer J. Natural Product Synthesis via 1,3-Dipolar Cycloadditions Organic Synthesis Set. 77-95. DOI: 10.1002/9783527620784.Ch12 |
0.379 |
|
| 2007 |
Kögl M, Brecker L, Warrass R, Mulzer J. Inside cover: total synthesis and configurational assignment of pasteurestin a and B (Angew. Chem. Int. Ed. 48/2007). Angewandte Chemie (International Ed. in English). 46: 9120. PMID 18061928 DOI: 10.1002/Anie.200790246 |
0.375 |
|
| 2007 |
Kögl M, Brecker L, Warrass R, Mulzer J. Total synthesis and configurational assignment of pasteurestin A and B. Angewandte Chemie (International Ed. in English). 46: 9320-2. PMID 17912731 DOI: 10.1002/Anie.200703457 |
0.382 |
|
| 2007 |
Innitzer A, Brecker L, Mulzer J. Functionalized cyclobutanes via Heck cyclization. Organic Letters. 9: 4431-4. PMID 17900129 DOI: 10.1021/Ol701697R |
0.355 |
|
| 2007 |
Tiefenbacher K, Mulzer J. Protecting-group-free formal synthesis of platensimycin. Angewandte Chemie (International Ed. in English). 46: 8074-5. PMID 17854110 DOI: 10.1002/Anie.200702852 |
0.361 |
|
| 2007 |
Barth R, Mulzer J. Total synthesis of efomycine M. Angewandte Chemie (International Ed. in English). 46: 5791-4. PMID 17594699 DOI: 10.1002/Anie.200701065 |
0.315 |
|
| 2007 |
Sheddan NA, Czybowski M, Mulzer J. Novel synthetic strategies for the preparation of prostacyclin and prostaglandin analogues--off the beaten track. Chemical Communications (Cambridge, England). 2107-20. PMID 17520108 DOI: 10.1039/B617693N |
0.364 |
|
| 2007 |
Tiefenbacher K, Arion VB, Mulzer J. A Diels-Alder approach to (-)-ovalicin. Angewandte Chemie (International Ed. in English). 46: 2690-3. PMID 17330826 DOI: 10.1002/Anie.200604781 |
0.352 |
|
| 2007 |
Felzmann W, Castagnolo D, Rosenbeiger D, Mulzer J. Crotylation versus propargylation: two routes for the synthesis of the C13-C18 fragment of the antibiotic branimycin. The Journal of Organic Chemistry. 72: 2182-6. PMID 17286444 DOI: 10.1021/Jo062502M |
0.652 |
|
| 2007 |
Marchart S, Mulzer J, Enev VS. cis-decalins from quinic acid: toward a synthesis of branimycin. Organic Letters. 9: 813-6. PMID 17266320 DOI: 10.1021/Ol0630189 |
0.392 |
|
| 2007 |
Mulzer J, Gaich T, Arion V. Synthesis Of The Cyclobutane Moiety Of Providencin Heterocycles. 74: 855-862. DOI: 10.3987/Com-07-S(W)79 |
0.472 |
|
| 2007 |
Schweizer E, Gaich T, Brecker L, Mulzer J. Synthetic studies towards the total synthesis of providencin Synthesis. 3807-3814. DOI: 10.1055/S-2007-990883 |
0.404 |
|
| 2007 |
Tiefenbacher K, Arion VB, Mulzer J. Synthesis of (-)-Ovalicin Synfacts. 2007: 906-906. DOI: 10.1055/S-2007-968833 |
0.457 |
|
| 2007 |
Enev VS, Drescher M, Mulzer J. Stereocontrolled formation of highly substituted cis-decalins via INOC annulation. An access to the branimycin core Tetrahedron. 63: 5930-5939. DOI: 10.1016/J.Tet.2007.02.126 |
0.338 |
|
| 2006 |
Sheddan NA, Mulzer J. Exploration of omega-side chain addition strategies for the syntheses of isocarbacyclin and 15R-16-(m-tolyl)-17,18,19,20-tetranorisocarbacyclin. Organic & Biomolecular Chemistry. 4: 4127-30. PMID 17312967 DOI: 10.1039/B611339G |
0.335 |
|
| 2006 |
Felzmann W, Arion VB, Mieusset JL, Mulzer J. A tether controlled exo-selective trans-annular Diels-Alder (TADA) reaction. Organic Letters. 8: 3849-51. PMID 16898833 DOI: 10.1021/Ol061510M |
0.399 |
|
| 2006 |
Sheddan NA, Mulzer J. Cross metathesis as a general strategy for the synthesis of prostacyclin and prostaglandin analogues. Organic Letters. 8: 3101-4. PMID 16805562 DOI: 10.1021/Ol061141U |
0.37 |
|
| 2006 |
Mulzer J, Castagnolo D, Felzmann W, Marchart S, Pilger C, Enev VS. Toward the synthesis of the antibiotic branimycin: novel approaches to highly substituted cis-decalin systems. Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 5992-6001. PMID 16710867 DOI: 10.1002/Chem.200600279 |
0.682 |
|
| 2006 |
Sheddan NA, Arion VB, Mulzer J. Effect of allylic and homoallylic substituents on cross metathesis: syntheses of prostaglandins F2α and J2 Tetrahedron Letters. 47: 6689-6693. DOI: 10.1016/J.Tetlet.2006.06.140 |
0.382 |
|
| 2006 |
Mulzer J, Hiersemann M, Buschmann J, Luger P. 1,2:5,6‐Di‐O‐isopropylidene‐α‐D‐gulofuranose as a Chiral Auxiliary in the Diastereoselective C Methylation of Ester Enolates. The Influence of the Base on the Stereochemistry of Enolate Formation and Alkylation Liebigs Annalen. 1996: 649-654. DOI: 10.1002/Jlac.199619960502 |
0.365 |
|
| 2006 |
Gaich T, Karig G, Martin HJ, Mulzer J. New solutions to the C-12,13 stereoproblem of epothilones B and D; synthesis of a 12,13-diol-acetonide epothilone B analog European Journal of Organic Chemistry. 3372-3394. DOI: 10.1002/Ejoc.200600113 |
0.444 |
|
| 2006 |
Schöllhorn B, Mulzer J. Stereocontrolled formation of three contiguous stereogenic centers by free radical cyclization - synthesis of (+)-iridomyrmecin and (-)-iso-iridomyrmecin - formal synthesis of δ-skythantine European Journal of Organic Chemistry. 901-908. DOI: 10.1002/Ejoc.200500711 |
0.443 |
|
| 2006 |
Mulzer J, Chucholowski A. Dreierdiastereoselektive Aldoladditionen von β‐Lacton‐enolaten an Aldehyde Angewandte Chemie. 94: 787-788. DOI: 10.1002/Ange.19820941015 |
0.394 |
|
| 2005 |
Gaich T, Mulzer J. Recent applications of olefin ring-closing metathesis (RCM) in the synthesis of biologically important alkaloids, terpenoids, polyketides and other secondary metabolites. Current Topics in Medicinal Chemistry. 5: 1473-94. PMID 16378488 DOI: 10.2174/156802605775009793 |
0.402 |
|
| 2005 |
Sheddan NA, Mulzer J. Access to isocarbacyclin derivatives via substrate-controlled enolate formation: total synthesis of 15-deoxy-16-(m-tolyl)- 17,18,19,20-tetranorisocarbacyclin. Organic Letters. 7: 5115-8. PMID 16268516 DOI: 10.1021/Ol0515762 |
0.414 |
|
| 2005 |
Gaich T, Mulzer J. Synthesis of epothilones via a silicon-tethered RCM reaction. Organic Letters. 7: 1311-3. PMID 15787494 DOI: 10.1021/Ol0500923 |
0.419 |
|
| 2005 |
Enev VS, Drescher M, Kählig H, Mulzer J. Aiming for branimycin: Synthesis of the cis-decalin core Synlett. 2227-2229. DOI: 10.1055/S-2005-872222 |
0.326 |
|
| 2005 |
Mulzer J, Sieg A, Brücher C, Müller D, Martin HJ. Horner-Wadsworth-Emmons reactions as a facile entry to biogenetic key substructures Synlett. 685-692. DOI: 10.1055/S-2005-863705 |
0.368 |
|
| 2005 |
Mulzer J, Giester G, Gilbert M. Toward a total synthesis of macrocyclic jatrophane diterpenes - Concise route to a highly functionalized cyclopentane key intermediate Helvetica Chimica Acta. 88: 1560-1579. DOI: 10.1002/Hlca.200590124 |
0.415 |
|
| 2005 |
Mulzer J, Steffen U, Martin HJ, Zorn L. Facially controlled C-methylation of oxolanyl and cyclopentyl acetate enolates: Application to the total synthesis of (+)-nephromopsinic acid European Journal of Organic Chemistry. 1028-1043. DOI: 10.1002/Ejoc.200400653 |
0.363 |
|
| 2004 |
Green MP, Pichlmair S, Marques MM, Martin HJ, Diwald O, Berger T, Mulzer J. Synthesis of analogue structures of the p-quinone methide moiety of kendomycin. Organic Letters. 6: 3131-4. PMID 15330605 DOI: 10.1021/Ol048825R |
0.365 |
|
| 2004 |
Mulzer J, Pichlmair S, Green MP, Marques MM, Martin HJ. Toward the synthesis of the carbacylic ansa antibiotic kendomycin. Proceedings of the National Academy of Sciences of the United States of America. 101: 11980-5. PMID 15277689 DOI: 10.1073/Pnas.0401503101 |
0.435 |
|
| 2004 |
Mulzer J, Martin HJ. Lessons learned from macrolide synthesis. Chemical Record (New York, N.Y.). 3: 258-70. PMID 14762826 DOI: 10.1002/Tcr.10069 |
0.444 |
|
| 2004 |
Mulzer J, Berger M. Total synthesis of the boron-containing ion carrier antibiotic macrodiolide tartrolon B. The Journal of Organic Chemistry. 69: 891-8. PMID 14750819 DOI: 10.1021/Jo035391P |
0.437 |
|
| 2004 |
Gilbert MW, Galkina A, Mulzer J. Toward the total syntheses of pepluanin A and euphosalicin: Concise route to a highly oxygenated cyclopentane as a common intermediate Synlett. 2558-2562. DOI: 10.1055/S-2004-834822 |
0.46 |
|
| 2004 |
Mulzer J, Strecker AR, Kattner L. A mechanistic study of the Hiyama-Nozaki allylation: Evidence for radical intermediates Tetrahedron Letters. 45: 8867-8870. DOI: 10.1016/J.Tetlet.2004.09.179 |
0.333 |
|
| 2004 |
Mulzer J, Kaselow U, Graske KD, Kühne H, Sieg A, Martin HJ. Stereocontrolled synthesis of all eight stereoisomers of the putative anti-androgen cyoctol Tetrahedron. 60: 9599-9614. DOI: 10.1016/J.Tet.2004.06.143 |
0.31 |
|
| 2003 |
Pichlmair S, Marques MM, Green MP, Martin HJ, Mulzer J. A novel approach toward the synthesis of kendomycin: selective synthesis of a C-aryl glycoside as a single atropisomer. Organic Letters. 5: 4657-9. PMID 14627408 DOI: 10.1021/Ol035846X |
0.452 |
|
| 2003 |
Heckrodt TJ, Mulzer J. Total synthesis of Elisabethin A: intramolecular Diels-Alder reaction under biomimetic conditions. Journal of the American Chemical Society. 125: 4680-1. PMID 12696865 DOI: 10.1021/Ja034397T |
0.445 |
|
| 2003 |
Ahmed A, Hoegenauer EK, Enev VS, Hanbauer M, Kaehlig H, Ohler E, Mulzer J. Total synthesis of the microtubule stabilizing antitumor agent laulimalide and some nonnatural analogues: the power of Sharpless' asymmetric epoxidation. The Journal of Organic Chemistry. 68: 3026-42. PMID 12688769 DOI: 10.1021/Jo026743F |
0.44 |
|
| 2003 |
and TJH, Mulzer J. Total Synthesis of Elisabethin A: Intramolecular Diels−Alder Reaction under Biomimetic Conditions [J. Am. Chem. Soc. 2003, 125, 4680−4681]. Journal of the American Chemical Society. 125: 9538-9538. DOI: 10.1021/Ja036029V |
0.392 |
|
| 2003 |
Riether D, Mulzer J. Total Synthesis of Cobyric Acid: Historical Development and Recent Synthetic Innovations European Journal of Organic Chemistry. 2003: 30-45. DOI: 10.1002/1099-0690(200301)2003:1<30::Aid-Ejoc30>3.0.Co;2-I |
0.406 |
|
| 2002 |
Hughes CC, Scharn D, Mulzer J, Trauner D. Borane-ammonia complexes stabilized by hydrogen bonding. Organic Letters. 4: 4109-11. PMID 12423098 DOI: 10.1021/Ol026865U |
0.597 |
|
| 2002 |
Langer O, Kählig H, Zierler-Gould K, Bats JW, Mulzer J. A bicyclic cispentacin derivative as a novel reverse turn inducer in a GnRH mimetic. The Journal of Organic Chemistry. 67: 6878-83. PMID 12353977 DOI: 10.1021/Jo025857O |
0.302 |
|
| 2002 |
Marques MMB, Pichlmair S, Martin HJ, Mulzer J. Stereocontrolled Synthesis of C-Arylglycosides Applied to the South West Fragment of the Antibiotic Kendomycin Synthesis. 2002: 2766-2770. DOI: 10.1055/S-2002-35990 |
0.451 |
|
| 2002 |
Mulzer J, Langer O. Synthesis and Conformational Analysis of a Novel Ansadipeptide Synthesis. 2002: 2091-2095. DOI: 10.1055/S-2002-34378 |
0.322 |
|
| 2002 |
Heckrodt TJ, Mulzer J. Synthesis of a Diels-Alder Precursor for the Elisabethin A Skeleton Synthesis. 2002: 1857-1866. DOI: 10.1055/S-2002-33919 |
0.435 |
|
| 2002 |
Pitts MR, Mulzer J. A chirally catalysed ene reaction in a novel formal total synthesis of the antitumor agent laulimalide Tetrahedron Letters. 43: 8471-8473. DOI: 10.1016/S0040-4039(02)02086-5 |
0.468 |
|
| 2002 |
Mulzer J, Hanbauer M. Total synthesis of the antitumor agent (-)-laulimalide Tetrahedron Letters. 43: 3381-3383. DOI: 10.1016/S0040-4039(02)00472-0 |
0.452 |
|
| 2002 |
Mulzer J, Öhler E, Enev VS, Hanbauer M. Grubbs' RCM in the total synthesis of the microtubule stabilizing drug laulimalide Advanced Synthesis and Catalysis. 344: 573-584. DOI: 10.1002/1615-4169(200208)344:6/7<573::Aid-Adsc573>3.0.Co;2-C |
0.411 |
|
| 2001 |
Enev VS, Kaehlig H, Mulzer J. Macrocyclization via allyl transfer: total synthesis of laulimalide. Journal of the American Chemical Society. 123: 10764-5. PMID 11674020 DOI: 10.1021/Ja016752Q |
0.376 |
|
| 2001 |
Mulzer J, Öhler E. An Intramolecular Case of Sharpless Kinetic Resolution: Total Synthesis of Laulimalide We thank the Austrian Research Foundation (FWF grant P13941-CHE) for financial support, Ing. Sabine Schneider for HPLC separations, and Prof. Hermann Kalchhauser and Dr. Hanspeter Kählig for NMR measurements. Angewandte Chemie (International Ed. in English). 40: 3842-3846. PMID 11668551 DOI: 10.1002/1521-3773(20011015)40:20<3842::Aid-Anie3842>3.0.Co;2-R |
0.342 |
|
| 2001 |
Högenauer K, Baumann K, Enz A, Mulzer J. Synthesis and acetylcholinesterase inhibition of 5-desamino huperzine A derivatives. Bioorganic & Medicinal Chemistry Letters. 11: 2627-30. PMID 11551765 DOI: 10.1016/S0960-894X(01)00518-2 |
0.394 |
|
| 2001 |
Martin HJ, Pojarliev P, Kählig H, Mulzer J. The 12,13-diol cyclization approach for a truly stereocontrolled total synthesis of epothilone B and the synthesis of a conformationally restrained analogue. Chemistry (Weinheim An Der Bergstrasse, Germany). 7: 2261-71. PMID 11411998 DOI: 10.1002/1521-3765(20010518)7:10<2261::Aid-Chem2261>3.0.Co;2-F |
0.431 |
|
| 2001 |
Högenauer K, Mulzer J. A novel palladium-catalyzed intramolecular redox reaction. Organic Letters. 3: 1495-7. PMID 11388850 DOI: 10.1021/Ol015813M |
0.377 |
|
| 2001 |
Ahmed A, Öhler E, Mulzer J. Synthesis of (S)-4-Methyl-3,6-dihydro-2H-pyran-2-carbaldehyde by Two-directional Ring Closing Metathesis: Application to the C27-C15-Fragment of Laulimalide Synthesis. 2001: 2007-2010. DOI: 10.1055/S-2001-17715 |
0.36 |
|
| 2001 |
Dorling EK, Öhler E, Mantoulidis A, Mulzer J. Concise Synthesis of the C3-C14-Fragment of the Antitumor Agent Laulimalide. Application of Jacobsen's HKR Reaction Synlett. 2001: 1105-1108. DOI: 10.1055/S-2001-15145 |
0.375 |
|
| 2001 |
Mulzer J, Czybowski M, Bats JW. Stereoselective synthesis of an isoprostane synthon via 8,12-free-radical cyclization Tetrahedron Letters. 42: 2961-2964. DOI: 10.1016/S0040-4039(01)00348-3 |
0.386 |
|
| 2001 |
Mulzer J. Book review: science of synthesis, houben-weyl methods of molecular transformations. vol. 10. fused five-membered hetarenes with one heteroatom. edited by e. jim thomas Angewandte Chemie. 40: 4293-4294. DOI: 10.1002/1521-3773(20011119)40:22<4293::Aid-Anie4293>3.0.Co;2-1 |
0.309 |
|
| 2001 |
Martin HJ, Drescher M, Kählig H, Schneider S, Mulzer J. Synthesis of the C1–C13 Fragment of Kendomycin: Atropisomerism around a C−Aryl Glycosidic Bond Financial support by the Austrian Science Foundation (FWF) is gratefully acknowledged. Angewandte Chemie. 40: 3186. DOI: 10.1002/1521-3773(20010903)40:17<3186::Aid-Anie3186>3.3.Co;2-N |
0.317 |
|
| 2001 |
Martin HJ, Drescher M, Khlig H, Schneider S, Mulzer J. Synthesis of the C1-C13 fragment of kendomycin: Atropisomerism around a C-aryl glycosidic bond Angewandte Chemie - International Edition. 40: 3186-3188. DOI: 10.1002/1521-3773(20010903)40:17<3186::Aid-Anie3186>3.0.Co;2-W |
0.305 |
|
| 2001 |
Mulzer J. Buchbesprechung: Science of Synthesis, Houben‐Weyl Methods of Molecular Transformations. Vol. 10. Fused Five‐Membered Hetarenes with one Heteroatom. Herausgegeben von E. Jim Thomas Angewandte Chemie. 113: 4425-4426. DOI: 10.1002/1521-3757(20011119)113:22<4425::Aid-Ange4425>3.0.Co;2-1 |
0.304 |
|
| 2001 |
Martin HJ, Drescher M, Kählig H, Schneider S, Mulzer J. Synthese des C1–C13‐Fragments von Kendomycin: Atropisomerie bezüglich einer glycosidischen C‐Aryl‐Bindung Angewandte Chemie. 113: 3287-3289. DOI: 10.1002/1521-3757(20010903)113:17<3287::Aid-Ange3287>3.0.Co;2-M |
0.315 |
|
| 2000 |
Mulzer J, Mantoulidis A, Ohler E. Total syntheses of epothilones B and D. The Journal of Organic Chemistry. 65: 7456-67. PMID 11076603 DOI: 10.1021/Jo0007480 |
0.371 |
|
| 2000 |
Mulzer J, Riether D. Efficient synthesis of the D-ring fragment of cobyric acid Organic Letters. 2: 3139-41. PMID 11009365 DOI: 10.1021/Ol006337N |
0.393 |
|
| 2000 |
Martin HJ, Drescher M, Mulzer J. How Stable Are Epoxides? A Novel Synthesis of Epothilone B. Angewandte Chemie (International Ed. in English). 39: 581-583. PMID 10671265 DOI: 10.1002/(Sici)1521-3773(20000204)39:3<581::Aid-Anie581>3.0.Co;2-W |
0.402 |
|
| 2000 |
Novak BH, Hudlicky T, Reed JW, Mulzer J, Trauner D. Morphine synthesis and biosynthesis - An update Current Organic Chemistry. 4: 343-362. DOI: 10.2174/1385272003376292 |
0.484 |
|
| 2000 |
Mulzer J, Hanbauer M. Synthesis of the C1-C12-dihydropyran segment of the antitumor agent laulimalide by ring closing metathesis Tetrahedron Letters. 41: 33-36. DOI: 10.1016/S0040-4039(99)02021-3 |
0.42 |
|
| 2000 |
Högenauer K, Baumann K, Mulzer J. Synthesis of (±)-desamino huperzine A Tetrahedron Letters. 41: 9229-9232. DOI: 10.1016/S0040-4039(00)01670-1 |
0.437 |
|
| 2000 |
Mulzer J, Karig G, Pojarliev P. A novel highly stereoselective total synthesis of epothilone B and of its (12R,13R) acetonide Tetrahedron Letters. 41: 7635-7638. DOI: 10.1016/S0040-4039(00)01318-6 |
0.412 |
|
| 2000 |
Dorling EK, Öhler E, Mulzer J. Synthesis of the C15–C27 fragment of the antitumor agent laulimalide Tetrahedron Letters. 41: 6323-6326. DOI: 10.1016/S0040-4039(00)00961-8 |
0.442 |
|
| 2000 |
Mulzer J, Schülzchen F, Bats J. Rigid Dipeptide Mimetics. Stereocontrolled Synthesis of All Eight Stereoisomers of 2-Oxo-3-( N -Cbz-amino)-1-azabicyclo[4.3.0]nonane-9-carboxylic Acid Ester Tetrahedron. 56: 4289-4298. DOI: 10.1016/S0040-4020(00)00355-0 |
0.36 |
|
| 2000 |
Mulzer J. Epothilone B and its Derivatives as Novel Antitumor Drugs: Total and Partial Synthesis and Biological Evaluation Monatshefte Fur Chemie. 131: 205-238. DOI: 10.1007/S007060070099 |
0.328 |
|
| 2000 |
Mulzer J, Bilow J, Wille G. The Anionic [1,3]-H-Shift Applied in Synthesis: A Novel Access to (+)-Citreoviral Journal Fur Praktische Chemie-Chemiker-Zeitung. 342: 773-778. DOI: 10.1002/1521-3897(200010)342:8<773::Aid-Prac773>3.0.Co;2-W |
0.427 |
|
| 1999 |
Dehnhardt C, McDonald M, Lee S, Ross HG, Mulzer J. Highly stereoselective synthesis of a chiral methyl group by a facially controlled sigmatropic [1,5]-hydrogen shift [11] Journal of the American Chemical Society. 121: 10848-10849. DOI: 10.1021/Ja992498E |
0.345 |
|
| 1999 |
Berger M, Mulzer J. Total synthesis of tartrolon B Journal of the American Chemical Society. 121: 8393-8394. DOI: 10.1021/Ja9919433 |
0.371 |
|
| 1999 |
Mulzer J, Riether D. Synthesis of the C-ring fragment of cobyric acid Tetrahedron Letters. 40: 6197-6199. DOI: 10.1016/S0040-4039(99)01134-X |
0.43 |
|
| 1999 |
Porth S, Bats JW, Trauner D, Giester G, Mulzer J. Insight into the Mechanism of the Saegusa Oxidation: Isolation of a Novel Palladium(0)–Tetraolefin Complex Angewandte Chemie. 38: 2015-2016. DOI: 10.1002/(Sici)1521-3773(19990712)38:13/14<2015::Aid-Anie2015>3.0.Co;2-# |
0.449 |
|
| 1999 |
Porth S, Bats JW, Trauner D, Giester G, Mulzer J. Einblick in den Mechanismus der Saegusa‐Oxidation: Isolierung eines neuartigen Palladium(0)‐Tetraolefin‐Komplexes Angewandte Chemie. 111: 2159-2161. DOI: 10.1002/(Sici)1521-3757(19990712)111:13/14<2159::Aid-Ange2159>3.0.Co;2-5 |
0.403 |
|
| 1999 |
Mulzer J, Trauner D. Practical synthesis of (-)-morphine Chirality. 11: 475-482. DOI: 10.1002/(Sici)1520-636X(1999)11:5/6<475::Aid-Chir20>3.0.Co;2-G |
0.564 |
|
| 1998 |
Trauner D, Bats JW, Werner A, Mulzer J. Synthesis of Enantiomerically Pure Morphine Alkaloids: The Hydrophenanthrene Route. The Journal of Organic Chemistry. 63: 5908-5918. PMID 11672195 DOI: 10.1021/Jo9805394 |
0.538 |
|
| 1998 |
Mulzer J, Schein K, Böhm I, Trauner D. About the use of molecular workbenches and platforms in organic synthesis Pure and Applied Chemistry. 70: 1487-1493. DOI: 10.1351/Pac199870081487 |
0.487 |
|
| 1998 |
Mulzer J, Böhm I, Bats JW. Ansa macrolides as molecular workbenches for stereoselective additions to achiral (E) olefins Tetrahedron Letters. 39: 9643-9646. DOI: 10.1016/S0040-4039(98)02275-8 |
0.309 |
|
| 1998 |
Mulzer J, Mantoulidis A, Öhler E. Easy access to the epothilone family - Synthesis of epothilone B Tetrahedron Letters. 39: 8633-8636. DOI: 10.1016/S0040-4039(98)02026-7 |
0.395 |
|
| 1998 |
Mulzer J, Berger M. Studies directed towards the total synthesis of the antibiotic macrodiolide tartrolon: EPC synthesis of the protected seco acid Tetrahedron Letters. 39: 803-806. DOI: 10.1016/S0040-4039(97)10761-4 |
0.458 |
|
| 1998 |
Mulzer J, Schein K, Bats JW, Buschmann J, Luger P. Ansa macrolides as molecular workbenches: Stereocontrolled syn additions to E olefins Angewandte Chemie - International Edition. 37: 1566-1569. DOI: 10.1002/(Sici)1521-3773(19980619)37:11<1566::Aid-Anie1566>3.0.Co;2-U |
0.311 |
|
| 1997 |
Mulzer J, Bats J, List B, Opatz T, Trauner D. The Phenanthrenone Approach to Opium Alkaloids: Formal Total Synthesis of Morphine by Sigmatropic Rearrangement Synlett. 1997: 441-444. DOI: 10.1055/S-1997-6135 |
0.574 |
|
| 1997 |
Mulzer J, Pietschmann C, Buschmann J, Luger P. Diastereoselective Grignard Additions to O-Protected Polyhydroxylated Ketones: A Reaction Controlled by Groundstate Conformation? Journal of Organic Chemistry. 62: 3938-3943. DOI: 10.1021/Jo961542V |
0.325 |
|
| 1997 |
Mulzer J, List B, Bats JW. Stereocontrolled synthesis of a nonracemic vitamin B12 A-B semicorrin Journal of the American Chemical Society. 119: 5512-5518. DOI: 10.1021/Ja9700515 |
0.451 |
|
| 1997 |
Mulzer J, Mantoulidis A, Öhler E. Synthesis of the C(11)-C(20) segment of the cytotoxic macrolide epothilone B Tetrahedron Letters. 38: 7725-7728. DOI: 10.1016/S0040-4039(97)10150-2 |
0.362 |
|
| 1996 |
Maguire RJ, Mulzer J, Bats JW. 1,4-Asymmetric Induction in the Chromium(II)- and Indium-Mediated Coupling of Allyl Bromides to Aldehydes. The Journal of Organic Chemistry. 61: 6936-6940. PMID 11667589 DOI: 10.1021/Jo960986O |
0.38 |
|
| 1996 |
Mulzer J, Meier A, Buschmann J, Luger P. Total Synthesis of cis- and trans-3-Hydroxy-D-proline and (+)-Detoxinine. The Journal of Organic Chemistry. 61: 566-572. PMID 11666976 DOI: 10.1021/Jo951444U |
0.323 |
|
| 1996 |
Mulzer J, Meier A, Buschmann J, Luger P. Synthesis of Enantiopure 1,2-Didehydropyrrolidine, D-Proline, and Oxazoline Derivatives via Staudinger-Aza-Wittig Cyclization of γ-Azido Aldehydes Synthesis. 1996: 123-132. DOI: 10.1055/S-1996-4162 |
0.436 |
|
| 1996 |
Mulzer J, Mantoulidis A. Synthesis of the C(1)-C(9) segment of the cytotoxic macrolides epothilon A and B Tetrahedron Letters. 37: 9179-9182. DOI: 10.1016/S0040-4039(96)02156-9 |
0.396 |
|
| 1996 |
Mulzer J, Martin HJ, List B. One-pot three component synthesis of α,β-unsaturated ketones Tetrahedron Letters. 37: 9177-9178. DOI: 10.1016/S0040-4039(96)02155-7 |
0.515 |
|
| 1996 |
Maguire RJ, Mulzer J, Bats JW. 1,4-Asymmetric induction in the Nozaki-Hiyama reaction Tetrahedron Letters. 37: 5487-5490. DOI: 10.1016/0040-4039(96)01161-6 |
0.373 |
|
| 1996 |
Mulzer J, List B. [2,3]-Wittig rearrangements of (trimethylsilyl)methyl allyl ethers Tetrahedron Letters. 37: 2403-2404. DOI: 10.1016/0040-4039(96)00321-8 |
0.431 |
|
| 1996 |
Mulzer J, Dürner G, Trauner D-D. Formal Total Synthesis of (—)-Morphine by Cuprate Conjugate Addition† Angewandte Chemie. 35: 2830-2832. DOI: 10.1002/Anie.199628301 |
0.356 |
|
| 1996 |
Mulzer J, Trauner D-D, Bats JW. Stereoselective Insertion of Ketenes into O,O‐Acetals: Synthesis of β‐Alkoxy Esters and 1,4‐Dioxepan‐5‐ones Angewandte Chemie. 35: 1970-1972. DOI: 10.1002/Anie.199619701 |
0.366 |
|
| 1996 |
Mulzer J, Dürner G, Trauner D. Formale Totalsynthese von (−)‐Morphin über konjugierte Cuprataddition Angewandte Chemie. 108: 3046-3048. DOI: 10.1002/Ange.19961082345 |
0.41 |
|
| 1996 |
Mulzer J, Trauner D, Bats JW. Stereoselektive Insertion von Ketenen in O, O‐Acetale: Synthese von β‐Alkoxyestern und 1,4‐Dioxepan‐5‐onen Angewandte Chemie. 108: 2093-2095. DOI: 10.1002/Ange.19961081722 |
0.423 |
|
| 1995 |
Mulzer J. New developments in the synthesis of polyketides and of chiral methyl groups Studies in Natural Products Chemistry. 18: 155-192. DOI: 10.1016/S1572-5995(96)80026-3 |
0.389 |
|
| 1995 |
Mulzer J, Meyer F, Buschmann J, Luger P. Asymmetric synthesis of the C-26-C-32 tetrahydropyran - moiety of Swinholide A by hetero-Diels-Alder reaction Tetrahedron Letters. 36: 3503-3506. DOI: 10.1016/0040-4039(95)00576-X |
0.374 |
|
| 1995 |
Schlecker W, Huth A, Ottow E, Mulzer J. Synthesis of 4-arylpyridines and substituted β-carbolines via 1,4-Grignard-addition to pyridinecarboxamides Tetrahedron. 51: 9531-9542. DOI: 10.1016/0040-4020(95)00596-Z |
0.371 |
|
| 1995 |
Schlecker W, Huth A, Ottow E, Mulzer J. Regioselective monometalation of 2,5-pyridinedicarboxamides with (2,2,6,6-tetramethylpiperidino)magnesium chloride (TMPMgCI) Liebigs Annalen. 1995: 1441-1446. DOI: 10.1002/Jlac.1995199508195 |
0.366 |
|
| 1995 |
Mulzer J, Pietschmann C, Schöllhorn B, Buschmann J, Luger P. New chiral building blocks from 1,2;5,6-di-O-isopropylidene-D-mannitol: Synthesis of C2-symmetrical and unsymmetrical mono- and bisepoxides and of a polyhydroxylated butenolide Liebigs Annalen. 1995: 1433-1439. DOI: 10.1002/Jlac.1995199508194 |
0.386 |
|
| 1995 |
Mulzer J, Graske K, Shanyoor M. A Short Synthesis of a Thromboxane B2 Key Intermediate from (R)‐2,3‐Isopropylideneglyceraldehyde. γ‐Lactones as Templates for Chemoselective cis‐Annulation of Pyranosides Liebigs Annalen. 1995: 593-598. DOI: 10.1002/Jlac.199519950482 |
0.449 |
|
| 1994 |
Mulzer J, Mohr J. Stereoselective Synthesis of the Bis-tetrahydrofuran Fragment (C-1-C-9) of Asteltoxin Journal of Organic Chemistry. 59: 1160-1165. DOI: 10.1021/Jo00084A039 |
0.476 |
|
| 1994 |
Mulzer J, List B. Highly stereoselective synthesis of tetrasubstituted alkenes via [2,3]-wittig rearrangement Tetrahedron Letters. 35: 9021-9024. DOI: 10.1016/0040-4039(94)88416-1 |
0.576 |
|
| 1994 |
Mulzer J. Asymmetric synthesis of the Novel Antidepressant Rolipram Journal Fur Praktische Chemie-Chemiker-Zeitung. 336: 287-291. DOI: 10.1002/Prac.19943360402 |
0.41 |
|
| 1994 |
Mulzer J, Kermanchahi AK, Buschmann J, Luger P. Asymmetric Synthesis of ent‐Corey Lactone Alcohol and its 12‐(all‐cis)‐ and 11‐Epimers via Free Radical 5‐exo‐trig‐C, C Cyclization European Journal of Organic Chemistry. 1994: 531-539. DOI: 10.1002/Jlac.199419940602 |
0.397 |
|
| 1994 |
Mulzer J, Schröder F, Lobbia A, Buschmann J, Luger P. Synthesis of a new unnatural amino acid with a benzodiazepine-containing side chain and incorporation into a tripeptide Angewandte Chemie. 33: 1737-1739. DOI: 10.1002/Anie.199417371 |
0.336 |
|
| 1994 |
Mulzer J, Schröder F, Lobbia A, Buschmann J, Luger P. Synthese einer neuen nichtnatürlichen Aminosäure mit einem Benzodiazepinrest in der Seitenkette und Einbau in ein Tripeptid Angewandte Chemie. 106: 1813-1815. DOI: 10.1002/Ange.19941061710 |
0.353 |
|
| 1993 |
Mulzer J, Scharp M. Practical asymmetric synthesis of hastanecine and dihydroxyheliotridane by a Claisen rearrangement/amine-epoxide-opening sequence Synthesis. 1993: 615-622. DOI: 10.1055/S-1993-25913 |
0.417 |
|
| 1993 |
Mulzer J, Salimi N, Hartl H. First asymmetric synthesis of (+)- and (−)-Roccellaric acid and dihydroprotolichesterinic acid Tetrahedron-Asymmetry. 4: 457-471. DOI: 10.1016/S0957-4166(00)86089-9 |
0.349 |
|
| 1993 |
Mulzer J, Shanyoor M. Highly diastereoselective synthesis of (−)-petasinecine via Ireland-Claisen-type rearrangement Tetrahedron Letters. 34: 6545-6548. DOI: 10.1016/0040-4039(93)88100-W |
0.39 |
|
| 1993 |
Mulzer J, Dupré S, Buschmann J, Luger P. Linear Total Synthesis of (–)‐ACRL Toxin III B Angewandte Chemie. 32: 1452-1454. DOI: 10.1002/Anie.199314521 |
0.347 |
|
| 1993 |
Mulzer J, Greifenberg S, Buschmann J, Luger P. Domino Reactions of 4‐Ene‐1,2,3‐triol Derivatives Angewandte Chemie. 32: 1173-1174. DOI: 10.1002/Anie.199311731 |
0.316 |
|
| 1992 |
Mulzer J, Mareski PA, Buschmann J, Luger P. Total synthesis of 6-epi-erythronolide derivatives Synthesis. 1992: 215-228. DOI: 10.1055/S-1992-34154 |
0.379 |
|
| 1992 |
Mulzer J, Dehmlow H, Buschmann J, Luger P. Stereocontrolled total synthesis of the unnatural enantiomers of castanospermine and 1-epi-castanospermine Journal of Organic Chemistry. 57: 3194-3202. DOI: 10.1021/Jo00037A043 |
0.432 |
|
| 1992 |
Schulz H, Liebscher J, Luger P, Quian M, Mulzer J. Selective mono, bis, and trisiminoformylation of 2,4,6-trialkyl-1,3,5-triazines : unusual enol acylenamine tautomerism of hydroxyalkenyl-1,3,5-triazines Journal of Heterocyclic Chemistry. 29: 1125-1132. DOI: 10.1002/Jhet.5570290515 |
0.356 |
|
| 1992 |
Mulzer J, Zuhse R, Schmiechen R. Enantioselective Synthesis of the Antidepressant Rolipram by Michael Addition to a Nitroolefin Angewandte Chemie. 31: 870-872. DOI: 10.1002/Anie.199208701 |
0.451 |
|
| 1992 |
Mulzer J, Zuhse R, Schmiechen R. Enantioselektive Synthese des Antidepressivums Rolipram durch Nitroolefin‐Michael‐Addition Angewandte Chemie. 104: 914-915. DOI: 10.1002/Ange.19921040734 |
0.316 |
|
| 1991 |
Mulzer J, Kattner L, Strecker AR, Schröder C, Buschmann J, Lehmann CW, Luger P. Highly Felkin-Anh selective Hiyama additions of chiral allylic bromides to aldehydes. Application to the first synthesis of nephromopsinic acid and its enantiomer Journal of the American Chemical Society. 113: 4218-4229. DOI: 10.1021/Ja00011A025 |
0.39 |
|
| 1991 |
Mulzer J, Kirstein HM, Buschmann J, Lehmann C, Luger P. Total synthesis of 9-dihydroerythronolide B derivatives and of erythronolide B Journal of the American Chemical Society. 113: 910-923. DOI: 10.1021/Ja00003A026 |
0.44 |
|
| 1991 |
Mulzer J, Seilz C, Reutter W. Enantiospecific synthesis of (2S,3S,5S)‐2‐acetamido‐2,4‐dideoxyhexopyranose (N‐acetyl‐4‐deoxy‐D‐mannosamine) from D‐glucose European Journal of Organic Chemistry. 1991: 957-960. DOI: 10.1002/Jlac.1991199101163 |
0.385 |
|
| 1991 |
Mulzer J, Seilz C, Luger P, Weber M, Reutter W. Total synthesis of all four diastereomers of 2-acetamido-2,4-dideoxy-D-hexapyranose as potential competitive inhibitors ofN-acetylneuraminic acid synthase Liebigs Annalen Der Chemie. 1991: 947-955. DOI: 10.1002/Jlac.1991199101162 |
0.381 |
|
| 1991 |
Mulzer J, Bock H, Eck W, Buschmann J, Luger P. Intramolecular Diels–Alder Reactions: Diastereofacial Selectivity and Coupling with an Aliphatic Claisen Rearrangement† Angewandte Chemie. 30: 414-416. DOI: 10.1002/Anie.199104141 |
0.31 |
|
| 1990 |
Mulzer J, Schöllhorn B. Enantio‐ and Regiocontrolled Synthesis of a Central Ionophoric Antibiotic Building Block by Sequential Opening of Two Epoxide Rings with Cuprate Reagents Angewandte Chemie. 29: 1476-1478. DOI: 10.1002/Anie.199014761 |
0.412 |
|
| 1990 |
Mulzer J, Schöllhorn B. Enantio‐ und regiokontrollierte Synthese eines zentralen Ionophor‐Antibiotica‐Bausteines durch sequentielle Öffnung zweier Epoxidringe mit Cuprat‐Reagentien Angewandte Chemie. 102: 1529-1530. DOI: 10.1002/Ange.19901021256 |
0.372 |
|
| 1990 |
Mulzer J, Kattner L. Doppelt stereodifferenzierende Hiyama‐Addition mit ungleichsinnigen Reaktanten; enantio‐ und diastereokontrollierte Synthese von Dihydrocanadensolid Angewandte Chemie. 102: 717-718. DOI: 10.1002/Ange.19901020634 |
0.371 |
|
| 1989 |
Mulzer J, Becker R, Brunner E. Synthesis of hydroxylated 1-azabicyclo[3.1.0]hexane and prolinol derivatives by stereo- and regiocontrolled Staudinger aminocyclization. Application to the nonproteinogenic amino acid (2S,3S,4S)-3-hydroxy-4-methylproline (HMP) and its enantiomer Journal of the American Chemical Society. 111: 7500-7504. DOI: 10.1021/Ja00201A033 |
0.329 |
|
| 1988 |
Mulzer J, Graske K, Kirste B. Asymmetric synthesis of carbacyclin precursors by Pauson‐Khand cyclization European Journal of Organic Chemistry. 1988: 891-897. DOI: 10.1002/Jlac.198819880913 |
0.465 |
|
| 1988 |
Mulzer J, Büttelmann B, Münch W. Synthesis of diastereomerically and enantiomerically pure (3S,4S)-statine European Journal of Organic Chemistry. 1988: 445-448. DOI: 10.1002/Jlac.198819880513 |
0.345 |
|
| 1988 |
Mulzer J, Kühl U, Huttner G, Evertz K. Facial selectivities and rate effects in the thermal [4+2] dimerization of arylated 1,3‐dienes. 1,5‐H shift versus dimerization of (Z)‐1,3‐Dienes Chemische Berichte. 121: 2231-2238. DOI: 10.1002/Cber.19881211223 |
0.322 |
|
| 1987 |
Mulzer J, Autenrieth-Ansorge L, Kirstein H, Matsuoka T, Muench W. Practical synthesis of diastereomerically and enantiomerically pure 2-methyl 1,3-diols from (R)-2,3-O-isopropylideneglyceraldehyde. Application to the C(1)-C(7) and C(9)-C(12) fragments of erythronolide B Journal of Organic Chemistry. 52: 3784-3789. DOI: 10.1021/Jo00226A011 |
0.34 |
|
| 1987 |
Mulzer J, Angermann A, Münch W, Schlichthörl G, Hentzschel A. Synthesis of (2R,3S)‐1,2,3‐Butanetriol Derivatives From (R)‐2,3‐O‐Isopropylideneglyceraldehyde and of the (2S,3R)‐Enantiomers From D‐Glucose. Application to the Synthesis of Enantiomerically Pure Muscarine European Journal of Organic Chemistry. 1987: 7-14. DOI: 10.1002/Jlac.198719870103 |
0.309 |
|
| 1987 |
Mulzer J. Book Review: Palladium Reagents in Organic Synthesis. By R. F. Heck Angewandte Chemie. 26: 593-594. DOI: 10.1002/Anie.198705933 |
0.314 |
|
| 1987 |
Mulzer J. Palladium Reagents in Organic Synthesis. Von R. F. Heck. Academic Press, New York 1985. XX, 461 S., geb. $ 99.00. – ISBN 0-12-336140-0 Angewandte Chemie. 99: 377-378. DOI: 10.1002/Ange.19870990437 |
0.32 |
|
| 1986 |
Mulzer J, Brand C. Enantioselective syntheses of D- and L-ribo- and arabino-C18- phytosphingosine from (R)-2,3-0-isopropylidene glyceraldehyde Tetrahedron. 42: 5961-5968. DOI: 10.1016/S0040-4020(01)96078-8 |
0.32 |
|
| 1986 |
Mulzer J, Salimi N. Stereocontrolled Synthesis of all Four Steroisomers of Verrucarinolactone from (R)‐2,3‐O‐Isopropylidene‐Glyceraldehyde European Journal of Organic Chemistry. 1986: 1172-1178. DOI: 10.1002/Jlac.198619860705 |
0.329 |
|
| 1986 |
Mulzer J, Lasalle Pd, Freißler A. Addition of crotylchromium(II) and dilithium propionate to (R)‐2,3‐O‐isopropylideneglyceraldehyde: Steric course and synthetic application in a formal synthesis of (+)‐ and (−)‐δ‐multistriatin European Journal of Organic Chemistry. 1986: 1152-1171. DOI: 10.1002/Jlac.198619860704 |
0.321 |
|
| 1986 |
Mulzer J, Angermann A, Münch W. Enantio‐ and Diastereocontrolled Synthesis of Chiral 1,2‐Diol Derivatives from (R)‐2,3‐Di‐O‐isopropylideneglyceraldehyde: endo‐ and exo‐brevicomin European Journal of Organic Chemistry. 1986: 825-838. DOI: 10.1002/Jlac.198619860504 |
0.318 |
|
| 1986 |
Mulzer J, Lasalle PD, Freissler A. Addition of Crotylchromium(II) and Dilithium Propionate to (R)-2,3-O-Isopropylideneglyceraldehyde: Steric Course and Synthetic Application in a Formal Synthesis of (+)- and (-)-δ-Multistriatin. Cheminform. 17. DOI: 10.1002/Chin.198646083 |
0.331 |
|
| 1986 |
Mulzer J, Lammer O. Enantioselective Diastereospecific Synthesis of anti-α-Alkyl-β-hydroxy Esters Through Cuprate Opening of Glycidic Esters. Cheminform. 17. DOI: 10.1002/Chin.198645063 |
0.356 |
|
| 1986 |
Mulzer J, Angermann A, Muench W. Enantio- and Diastereocontrolled Synthesis of Chiral 1,2-Diol Derivatives from (R)-2,3-Di-O-isopropylideneglyceraldehyde: endo- and exo-Brevicomin. Cheminform. 17. DOI: 10.1002/Chin.198636333 |
0.363 |
|
| 1986 |
Mulzer J, Lammer O. Enantioselective diastereospecific synthesis of anti-α-alkyl-β-hydroxy esters through cuprate opening of glycidic esters Chemische Berichte. 119: 2178-2190. DOI: 10.1002/Cber.19861190713 |
0.349 |
|
| 1986 |
Mulzer J, Chucholowski A. Stereocontrolled Synthesis of Paraconates from β‐Lactones; Stereochemistry of Electrophilic Additions to Endocyclic Paraconate‐Enolates Angewandte Chemie. 25: 655-656. DOI: 10.1002/Anie.198606551 |
0.485 |
|
| 1985 |
Mulzer J, Kappert M, Huttner G, Jibril I. Uncatalyzed asymmetric diels-alder addition of cyclopentadiene to (E)- and (Z) - (R) -4,5-di-O-isopropylidene-pent-2-enonates Tetrahedron Letters. 26: 1631-1634. DOI: 10.1016/S0040-4039(00)98570-8 |
0.342 |
|
| 1985 |
Mulzer J, Kappert M, Huttner G, Jibril I. Diastereo- And Enantioselective Synthesis Of Vicinal Threo- Or Erythro-Dihydroxy Derivatives Cheminform. 16. DOI: 10.1002/Chin.198501101 |
0.469 |
|
| 1985 |
Mulzer J. Strategies and Tactics in Organic Synthesis. Herausgegeben von T. Lindberg. Academic Press, New York 1984. XIV, 370 S., geb. $ 57.00. ‐ ISBN 0‐12‐450280‐6 Angewandte Chemie. 97: 528-529. DOI: 10.1002/Ange.19850970633 |
0.301 |
|
| 1984 |
Mulzer J, Lasalle PD, Chucholowski A, Blaschek U, Brüntrup G, Jibril I, Huttner G. Stereoselective additions to carboxylic acid dianions and β-lactone substituted ester enolates Tetrahedron. 40: 2211-2218. DOI: 10.1016/0040-4020(84)80003-4 |
0.351 |
|
| 1984 |
Mulzer J. New Alkaloid Syntheses Cheminform. 15. DOI: 10.1002/Chin.198447374 |
0.314 |
|
| 1984 |
Mulzer J, Lasalle PD, Chucholowski A, Blaschek U, Bruentrup G, Jibril I, Huttner G. Stereoselective additions to carboxylic acid dianions and β-lactone substituted ester enolates: application to the synthesis of racemic epi-blastmycinone, δ-multistriatine, paraconic esters and lignantype dilactones Tetrahedron. 15: 2211-2218. DOI: 10.1002/Chin.198440069 |
0.401 |
|
| 1984 |
Mulzer J, Kappert M, Huttner G, Jibril I. Optional Diastereo‐ and Enantioselective Synthesis of Vicinal threo‐ or erythro‐Dihydroxy Derivatives Angewandte Chemie. 23: 704-705. DOI: 10.1002/Anie.198407041 |
0.46 |
|
| 1984 |
Mulzer J, Kappert M, Huttner G, Jibril I. Wahlweise diastereo‐ und enantioselektive Synthese von vicinalen threo‐ oder erythro‐ Dihydroxyderivaten Angewandte Chemie. 96: 726-727. DOI: 10.1002/Ange.19840960936 |
0.378 |
|
| 1983 |
Mulzer J, Chucholowski A, Lammer O, Jibril I, Huttner G. Diastereoselective Michael additions of β-lactone enolates to dimethyl maleate Journal of the Chemical Society, Chemical Communications. 869-871. DOI: 10.1039/C39830000869 |
0.314 |
|
| 1983 |
Mulzer J, Angermann A. On the steric course of the addition of some organometallic reagents to (R)-2,3-isopropylidene glyceraldehyde. Synthesis of optically active α-benzyloxy aldehydes, alcohols, carboxylic acids and 1,2-diols Tetrahedron Letters. 24: 2843-2846. DOI: 10.1016/S0040-4039(00)88039-9 |
0.302 |
|
| 1983 |
Mulzer J, Lasalle PD. Synthesis Of (S)-((2-Phenylmethoxy)Ethyl)Oxirane Cheminform. 14. DOI: 10.1002/Chin.198318137 |
0.391 |
|
| 1983 |
Mulzer J, Lammer O. Olefins from β‐Hydroxycarboxylic Acids ‐ Synthesis of Isomerically Pure α‐ and β‐Asarone Angewandte Chemie. 22: 628-629. DOI: 10.1002/Anie.198308870 |
0.34 |
|
| 1982 |
Mulzer J, Chucholowski A. Three‐Center Diastereoselective Aldol Additions of β‐Lactone Enolates to Aldehydes Angewandte Chemie. 21: 777-778. DOI: 10.1002/Anie.198207771 |
0.448 |
|
| 1980 |
Mulzer J, Bruentrup G, Finke J, Zippel M. Aldol addition = cycloaddition without cycloadduct formation 2 Cheminform. 11. DOI: 10.1002/Chin.198012097 |
0.364 |
|
| 1980 |
Mulzer J, Kerkmann T. 2-Thietanimines from α-Deprotonated β-Lactones and Phenyl Isothiocyanate—A Novel Four-Membered Ring/Four-Membered Ring Recyclization† Angewandte Chemie. 19: 466-468. DOI: 10.1002/Anie.198004661 |
0.316 |
|
| 1979 |
Mulzer J, Pointner A, Chucholowski A, Brüntrup G. threo-3-Hydroxycarboxylic acids as key intermediates in a highly stereoselective synthesis of (Z)- and (E)-olefins and enol ethers Journal of the Chemical Society, Chemical Communications. 52-54. DOI: 10.1039/C39790000052 |
0.368 |
|
| 1979 |
Mulzer J, Bruentrup G, Finke J, Zippel M. Aldol addition = cycloaddition without cycloadduct formation 2 Journal of the American Chemical Society. 101: 7723-7725. DOI: 10.1021/Ja00520A020 |
0.364 |
|
| 1979 |
Mulzer J, Brüntrup G. The decarboxyla tive dehydration of 3-hydroxycarboxylic acids with dimethyl-formamide-dimethylacetal - evidence for a zwitterionic intermediate Tetrahedron Letters. 20: 1909-1912. DOI: 10.1016/S0040-4039(01)86876-3 |
0.3 |
|
| 1979 |
Mulzer J, Pointer A, Chucholowski A, Bruentrup G. Threo-3-Hydroxycarboxylic Acids As Key Intermediates In A Highly Stereoselective Synthesis Of (Z)- And (E)-Olefins And Enol Ethers Cheminform. 10. DOI: 10.1002/Chin.197921184 |
0.408 |
|
| 1979 |
Mulzer J, Brütrup G. Stereospecific Synthesis of γ‐Lactones by Dyotropic Wagner‐Meerwein Rearrangement Angewandte Chemie. 18: 793-794. DOI: 10.1002/Anie.197907931 |
0.472 |
|
| 1979 |
Mulzer J, Brüntrup G. Stereospezifische Synthese von γ‐Lactonen durch dyotrope Wagner‐Meerwein‐Umlagerung Angewandte Chemie. 91: 840-841. DOI: 10.1002/Ange.19790911010 |
0.385 |
|
| 1978 |
Mulzer J, Kühl U, Brüntrup G. The decarboxylative dehydration of 4.5-unsaturated 3-hydroxycarboxylic acids with dimethylformamide dimethylacetal - an efficient synthesis of sensitive 1.3-dienes. Tetrahedron Letters. 19: 2953-2954. DOI: 10.1016/S0040-4039(01)94909-3 |
0.381 |
|
| 1977 |
Mulzer J, Segner J, Brüntrup G. Stereoselective synthesis of threo-3-hydroxycarboxylic acids. Stereocheminstry of an aldoltype addition under kinetic and thermodynamic control. Tetrahedron Letters. 18: 4651-4654. DOI: 10.1016/S0040-4039(01)83592-9 |
0.373 |
|
| 1977 |
Mulzer J, Brüntrup G. Decarboxylative Dehydration of β‐Hydroxycarboxylic Acids by Redox Condensation: A Novel Olefin Synthesis Angewandte Chemie. 16: 255-256. DOI: 10.1002/Anie.197702551 |
0.403 |
|
| Show low-probability matches. |
