| Year |
Citation |
Score |
| 2006 |
Staab HA, Saupe T, Krieger C. 4,5‐Bis(dimethylamino)fluoren, ein neuer „Protonenschwamm”︁ Angewandte Chemie. 95: 748-749. DOI: 10.1002/Ange.19830950924 |
0.359 |
|
| 2001 |
Bauer H, Stier F, Petry C, Knorr A, Stadler C, Staab HA. Phenothiazine−Bipyridinium Cyclophanes European Journal of Organic Chemistry. 2001: 3255-3278. DOI: 10.1002/1099-0690(200109)2001:17<3255::Aid-Ejoc3255>3.0.Co;2-0 |
0.312 |
|
| 2000 |
Staab HA, Kirsch A, Barth T, Krieger C, Neugebauer FA. Isomeric tetrakis(dimethylamino)naphthalenes: Syntheses, structure- dependence of basicities, crystal structures, and physical properties European Journal of Organic Chemistry. 1617-1622. DOI: 10.1002/(Sici)1099-0690(200004)2000:8<1617::Aid-Ejoc1617>3.0.Co;2-C |
0.353 |
|
| 2000 |
Staab HA, Elbl-Weiser K, Krieger C. Syntheses, Structures and Basicities of 1,2,4,5‐Tetrakis(dimethylamino)benzene and 2,3,6,7‐Tetrakis(dimethylamino)naphthalene European Journal of Organic Chemistry. 2000: 327-333. DOI: 10.1002/(Sici)1099-0690(200001)2000:2<327::Aid-Ejoc327>3.0.Co;2-Z |
0.353 |
|
| 1999 |
Pullen SH, Edington MD, Studer-Martinez SL, Simon JD, Staab HA. Experimental Verification of the Through-Bond Mechanisms of Electron Transfer in Bridged Donor-Acceptor Complexes Journal of Physical Chemistry A. 103: 2740-2743. DOI: 10.1021/Jp984761O |
0.323 |
|
| 1999 |
Staab HA, Nikolic S, Krieger C. Pyromellitic diimide-porphyrin cyclophanes: Syntheses, transannular interactions and structure analysis European Journal of Organic Chemistry. 1999: 1459-1470. DOI: 10.1002/(Sici)1099-0690(199906)1999:6<1459::Aid-Ejoc1459>3.0.Co;2-7 |
0.395 |
|
| 1998 |
Staab HA, Weikard J, Rückemann A, Schwögler A. Porphyrin-Cyclophanes with 7,7,8,8-Tetracyanoquinodimethane as an Especially Strong Electron-Acceptor: Syntheses, Properties, Electron-Transfer Interactions European Journal of Organic Chemistry. 2703-2712. DOI: 10.1002/(Sici)1099-0690(199812)1998:12<2703::Aid-Ejoc2703>3.0.Co;2-I |
0.358 |
|
| 1998 |
Staab HA, Kratzer B, Quazzotti S. Distance dependence of photoinduced electron-transfer: Syntheses and properties of biphenylene-spacered porphyrin-quinone cyclophanes European Journal of Organic Chemistry. 2149-2160. DOI: 10.1002/(Sici)1099-0690(199810)1998:10<2149::Aid-Ejoc2149>3.0.Co;2-E |
0.351 |
|
| 1998 |
Wartini AR, Staab HA, Neugebauer FA. Intramolecular electron transfer between terminal 1,4-dimethoxybenzene units in radical cations with a [2.2](1,4)naphthalenophane, [2.2](1,4)anthracenophane, and pentacene skeleton European Journal of Organic Chemistry. 1161-1170. DOI: 10.1002/(Sici)1099-0690(199806)1998:6<1161::Aid-Ejoc1161>3.0.Co;2-1 |
0.337 |
|
| 1998 |
Wartini AR, Valenzuela J, Staab HA, Neugebauer FA. [2.2]Paracyclophane‐4,7,12,15‐tetrone, [2.2](1,4)Naphthalenophane‐4,7,14,17‐tetrone, and 1,4,8,11‐Pentacenetetrone Radical Anions − A Comparative ESR Study European Journal of Organic Chemistry. 1998: 221-227. DOI: 10.1002/(Sici)1099-0690(199802)1998:2<221::Aid-Ejoc221>3.0.Co;2-Y |
0.33 |
|
| 1998 |
Wartini AR, Valenzuela J, Staab HA, Neugebauer FA. Intramolecular Electron Transfer between 2,5‐Dimethoxy‐1,4‐phenylene Units in [n.n]Paracyclophane Radical Cations European Journal of Organic Chemistry. 1998: 139-148. DOI: 10.1002/(Sici)1099-0690(199801)1998:1<139::Aid-Ejoc139>3.0.Co;2-6 |
0.316 |
|
| 1997 |
Staab HA, Feurer A, Krieger C, Kumar AS. Photoinduced electron-transfer in porphyrin-quinone cyclophanes, 15. Distance dependence of photoinduced electron-transfer: Syntheses and structures of naphthalene-spacered porphyrin-quinone cyclophanes Liebigs Annales. 2321-2336. DOI: 10.1002/Jlac.199719971121 |
0.377 |
|
| 1997 |
Staab HA, Zhang D, Krieger C. New Electron Donor−Acceptor Compounds, 51. [3](N,N)−1,8;4,5−Naphthalenetetracarboxdiimido− [3](2,7)Pyrenophane and Its [4,4]Cyclophane Homologue Liebigs Annalen. 1997: 1551-1556. DOI: 10.1002/Jlac.199719970735 |
0.385 |
|
| 1997 |
Staab HA, Krieger C, Hieber G, Oberdorf K. 1,8-Bis(Dimethylamino)-4,5-Dihydroxynaphthalin : Ein Neutraler, Intramolekular Protonierter Protonenschwamm Mit Zwitterionischer Struktur Angewandte Chemie. 109: 1946-1949. DOI: 10.1002/Ange.19971091718 |
0.306 |
|
| 1996 |
Frank M, Peraus K, Staab HA. Exploring the Conformational Behavior of Rigid Porphyrin-Quinone Systems by High-Temperature MD Simulations and Temperature-Dependent 1H-NMR Experiments Journal of Molecular Modeling. 2: 383-385. DOI: 10.1007/S0089460020383 |
0.339 |
|
| 1995 |
Staab HA, Diehm M, Krieger C. Synthesis, structure and 'proton sponge' properties of 1,12-bis(dimethylamino)benzo[c]phenanthrene Tetrahedron Letters. 36: 2967-2970. DOI: 10.1016/0040-4039(95)00441-E |
0.338 |
|
| 1995 |
Staab HA, Kanellakopulos J, Kirsch P, Krieger C. π…π interactions of flavins, 5. Syntheses, structures and physical properties of flavin systems with covalent bonding to π donors and π acceptors (quinones) Liebigs Annalen. 1995: 1827-1836. DOI: 10.1002/Jlac.1995199510256 |
0.646 |
|
| 1994 |
Lipson M, McGarry PF, Koptyug IV, Staab HA, Turro NJ, Doetschman DC. Electron spin resonance of the lowest excited triplet states .alpha.-Oxo[1.n]paracyclophanes [cyclophanobenzophenones]. Effect of molecular geometry on the electronic character of the triplet state The Journal of Physical Chemistry. 98: 7504-7512. DOI: 10.1021/J100082A020 |
0.318 |
|
| 1994 |
Staab HA, Döhling A, Voit P, Dernbach M. Syntheses of a fourfold-bridged porphyrin-quinone cyclophane and its zinc complex Tetrahedron Letters. 35: 7617-7620. DOI: 10.1016/S0040-4039(00)78357-2 |
0.351 |
|
| 1994 |
Kirsch A, Krieger C, Staab HA, Neugebauer FA. 1,2,5,6- and 1,2,7,8-tetrakis(dimethylamino)naphthalenes and their dications: Syntheses and properties Tetrahedron Letters. 35: 8365-8368. DOI: 10.1016/S0040-4039(00)74408-X |
0.36 |
|
| 1994 |
Staab HA, Diehm M, Krieger C. Synthesis, structure and basicity of 1,16-diaza[6]helicene Tetrahedron Letters. 35: 8357-8360. DOI: 10.1016/S0040-4039(00)74406-6 |
0.327 |
|
| 1994 |
Bauer H, Matz V, Lang M, Krieger C, Staab HA. Oligooxa[3n.3]paracyclophane Quinhydrones — Cation-Induced Charge-Transfer Absorptions and Structures of the Metal Complexes Chemische Berichte. 127: 1993-2008. DOI: 10.1002/Cber.19941271024 |
0.323 |
|
| 1994 |
Staab HA, Zipplies MF, Müller T, Storch M, Krieger C. Pyridinio‐isoalloxazinophanes as Model Systems for Active‐Site Complexes in Flavoenzymes: Syntheses, X‐Ray Structure Analyses and Spectroscopic Properties Chemische Berichte. 127: 1667-1680. DOI: 10.1002/Cber.19941270918 |
0.344 |
|
| 1994 |
Staab HA, Kirsch P, Zipplies MF, Weinges A, Krieger C. [3.3]Isoalloxazinophanes and arene-bridged bis(isoalloxazines): syntheses, characterizations and properties related to intramolecular interactions Chemische Berichte. 127: 1653-1665. DOI: 10.1002/Cber.19941270917 |
0.648 |
|
| 1994 |
Staab HA, Krieger C, Anders C, Rückemann A. Zinc complexes of porphyrin-quinone cyclophanes: syntheses, structures and electron-transfer-related properties Chemische Berichte. 127: 231-236. DOI: 10.1002/Cber.19941270133 |
0.338 |
|
| 1994 |
Staab HA, Carell T, Döhling A. Syntheses and Properties of New Quinone-Bridged Diphenyl- and Tetraphenylporphyrins Chemische Berichte. 127: 223-229. DOI: 10.1002/Cber.19941270132 |
0.651 |
|
| 1994 |
Staab HA, Tercel M, Fischer R, Krieger C. Synthesis and properties of a vertically stacked porphyrin-quinone(1)-quinone(2) cyclophane Angewandte Chemie (International Edition in English). 33: 1463-1466. DOI: 10.1002/Anie.199414631 |
0.323 |
|
| 1994 |
Staab HA, Carell T. Synthese und Eigenschaften eines vertikal gestapelten Porphyrin(1)‐Porphyrin(2)‐Chinon‐Cyclophans Angewandte Chemie. 106: 1534-1536. DOI: 10.1002/Ange.19941061413 |
0.657 |
|
| 1994 |
Staab HA, Tercel M, Fischer R, Krieger C. Synthese und Eigenschaften eines vertikal gestapelten Porphyrin‐Chinon(1)‐Chinon(2)‐Cyclophans Angewandte Chemie. 106: 1531-1534. DOI: 10.1002/Ange.19941061412 |
0.385 |
|
| 1993 |
Barth T, Krieger G, Staab HA, Neugebauer FA. The dication of 1,4,5,8-tetrakis(dimethylamino)naphthalene: Properties, crystal structure and a comparison with the dication of 1,4-bis(dimethylamino) benzene Journal of the Chemical Society, Chemical Communications. 1129-1131. DOI: 10.1039/C39930001129 |
0.317 |
|
| 1993 |
Pöllinger F, Heitele H, Michel-Beyerle ME, Tercel M, Staab HA. Stacked porphyrin-quinone triads as models for the primary charge-separation in photosynthesis Chemical Physics Letters. 209: 251-257. DOI: 10.1016/0009-2614(93)80103-V |
0.31 |
|
| 1993 |
Krieger C, Dernbach M, Voit G, Carell T, Staab HA. Photoinduced Electron Transfer in Porphyrin‐Quinone Cyclophanes, 8 Conformational Mobility and Crystal Structures of Porphyrin‐Quinone Cyclophanes Chemische Berichte. 126: 811-821. DOI: 10.1002/Cber.19931260336 |
0.636 |
|
| 1992 |
Heitele H, Pöllinger F, Kremer K, Michel-Beyerle ME, Futscher M, Voit G, Weiser J, Staab HA. Electron transfer in porphyrin—quinone cyclophanes Chemical Physics Letters. 188: 270-278. DOI: 10.1016/0009-2614(92)90021-E |
0.336 |
|
| 1992 |
Frey W, Klann R, Laermer F, Elsaesser T, Baumann E, Futscher M, Staab HA. Electron transfer in porphyrin-quinone cyclophanes studied on the pico- and femto-second time scale Chemical Physics Letters. 190: 567-573. DOI: 10.1016/0009-2614(92)85192-D |
0.316 |
|
| 1992 |
Staab HA, Voit G, Weiser J, Futscher M. Photoinduced electron transfer in porphyrin‐quinone cyclophanes, 7. Porphyrin‐quinone cyclophanes with gradually varied acceptor strength: Physical properties related to electron transfer Chemische Berichte. 125: 2303-2310. DOI: 10.1002/Cber.19921251018 |
0.346 |
|
| 1992 |
Staab HA, Weiser J, Futscher M, Voit G, Rückemann A, Anders C. Photoinduced electron transfer in porphyrin‐quinone cyclophanes, 6. Porphyrin‐quinone cyclophanes with gradually varied acceptor strength: Syntheses and characterizations Chemische Berichte. 125: 2285-2301. DOI: 10.1002/Cber.19921251017 |
0.373 |
|
| 1992 |
Staab HA, Weiser J, Baumann E. Photoinduced electron transfer in porphyrin‐quinone cyclophanes, 5. Quinone‐porphyrin‐quinone and quinone‐porphyrin‐donor cyclophanes: Syntheses, structures and electron‐transfer‐related properties Chemische Berichte. 125: 2275-2283. DOI: 10.1002/Cber.19921251016 |
0.336 |
|
| 1991 |
Staab HA, Döhling A, Krieger C. Electron donor-acceptor [3.3]metacyclophanes: charge-transfer absorption of syn- and anti-isomers Tetrahedron Letters. 32: 2215-2218. DOI: 10.1016/S0040-4039(00)79684-5 |
0.352 |
|
| 1991 |
Asami M, Krieger C, Staab HA. New orthopara- and orthometacyclophanes Tetrahedron Letters. 32: 2117-2120. DOI: 10.1016/S0040-4039(00)71251-2 |
0.34 |
|
| 1991 |
Barth T, Krieger C, Neugebauer FA, Staab HA. 1,4,5,8‐Tetrakis(dimethylamino)naphthalene: Synthesis, Structure, “Proton Sponge” and Electron Donor Properties Angewandte Chemie. 30: 1028-1030. DOI: 10.1002/Anie.199110281 |
0.351 |
|
| 1991 |
Barth T, Krieger C, Neugebauer FA, Staab HA. 1,4,5,8‐Tetrakis(dimethylamino)naphthalin: Synthese, Struktur, „Protonenschwamm”︁‐ und Elektronendonor‐Eigenschaften Angewandte Chemie. 103: 1006-1008. DOI: 10.1002/Ange.19911030828 |
0.382 |
|
| 1990 |
Eiermann U, Krieger C, Neugebauer FA, Staab HA. [2.2](2,6)‐ and [2.2](2,5)Pyrazinophanes: Synthesis and Molecular Structure Chemische Berichte. 123: 523-533. DOI: 10.1002/Cber.19901230319 |
0.353 |
|
| 1989 |
Turro NJ, Gould IR, Liu J, Jenks WS, Staab H, Alt R. Investigations of the influence of molecular geometry on the spectroscopic and photochemical properties of .alpha.-oxo[1.n]paracyclophanes (cyclophanobenzophenones) Journal of the American Chemical Society. 111: 6378-6383. DOI: 10.1021/Ja00198A059 |
0.34 |
|
| 1989 |
Mauzerall D, Weiser J, Staab H. Electron transfer in photoexcited porphyrin quinone cyclophanes Tetrahedron. 45: 4807-4814. DOI: 10.1016/S0040-4020(01)85153-X |
0.328 |
|
| 1989 |
Staab HA, Zirnstein MA, Krieger C. Benzo[1,2‐h:4,3‐h′]diquinoline (“1,14‐Diaza[5]helicene”): Synthesis, Structure, and Properties Angewandte Chemie. 28: 86-88. DOI: 10.1002/Anie.198900861 |
0.315 |
|
| 1989 |
Krieger C, Newsom I, Zirnstein MA, Staab HA. Strukturen von Chino[7,8‐h]chinolin und Chino[8,7‐h]chinolin Angewandte Chemie. 101: 72-73. DOI: 10.1002/Ange.19891010119 |
0.302 |
|
| 1988 |
Staab HA, Krieger C, Höne M. Structuresof 2,2′-bis(dimethylamino)biphenyl and its monohydrobromide) Tetrahedron Letters. 29: 5629-5632. DOI: 10.1016/S0040-4039(00)80830-8 |
0.324 |
|
| 1988 |
Gleiter R, Schäfer W, Staab HA. Photoelektronen‐Spektren von Donor‐Akzeptor‐Cyclophanen Chemische Berichte. 121: 1257-1264. DOI: 10.1002/Cber.19881210708 |
0.322 |
|
| 1988 |
Staab HA, Saupe T. “Proton Sponges” and the Geometry of Hydrogen Bonds: Aromatic Nitrogen Bases with Exceptional Basicities Angewandte Chemie. 27: 865-879. DOI: 10.1002/Anie.198808653 |
0.317 |
|
| 1988 |
Staab HA, Saupe T. «Protonenschwamm» ― Verbindungen und die Geometrie von Wasserstoffbrücken: Aromatische Stickstoffbasen mit ungewöhnlicher Basizität Angewandte Chemie. 100: 895-909. DOI: 10.1002/Ange.19881000704 |
0.326 |
|
| 1987 |
Staab HA, Krieger C, Wahl P, Kay K. Electron Donor‐Acceptor Compounds, 46 Molecular Structures and Charge‐Transfer Absorptions of [2.2]‐, [3.3]‐, and [4.4] Paracyclophanes with Tetracyanobenzene as Acceptor Unit Chemische Berichte. 120: 551-558. DOI: 10.1002/Cber.19871200415 |
0.386 |
|
| 1987 |
Staab HA, Wahl P, Kay K. Electron Donor-Acceptor Compounds, 45 Syntheses of [2.2]-, [3.3]-, and [4.4]Paracyclophanes with 1,2,4,5-Tetracyanobenzene Units as Electron Acceptors Chemische Berichte. 120: 541-549. DOI: 10.1002/Cber.19871200414 |
0.415 |
|
| 1987 |
Staab HA, Gabel G, Krieger C. Electron donor-acceptor compounds, 44 synthesis, molecular structure, and electron-donor properties of pseudogem-5,8,14,17-Tetrakis(dimethylamino)[3.3]paracyclophane Chemische Berichte. 120: 269-273. DOI: 10.1002/Cber.19871200304 |
0.404 |
|
| 1987 |
Staab HA, Herbst W, Krieger C. Darstellung und Strukturanalyse eines stabilen 9,10‐Anthrachinodimethans Chemische Berichte. 120: 93-95. DOI: 10.1002/Cber.19871200117 |
0.312 |
|
| 1987 |
Staab HA, Matzke G, Krieger C. 9,12,22,25‐Tetramethoxy[7.7]paracyclophan‐4,17‐dion:Synthese und Molekülstruktur Chemische Berichte. 120: 89-91. DOI: 10.1002/Cber.19871200116 |
0.407 |
|
| 1986 |
Staab HA, Elbl K, Krieger C. Protonation of 1,2,4,5-tetrakis(dimethylamino)benzene Tetrahedron Letters. 27: 5719-5722. DOI: 10.1016/S0040-4039(00)85309-5 |
0.316 |
|
| 1986 |
Rentzea M, Saupe T, Staab HA. Proximity effects in the mass spectra of crowded bis(dimethylamino)arenes, I, intramolecular cyclization of 'proton sponges' under electron impact Tetrahedron Letters. 27: 5715-5718. DOI: 10.1016/S0040-4039(00)85308-3 |
0.327 |
|
| 1986 |
Schweitzer D, Hausser KH, Vogler H, Staab HA, Boekelheide V. Electronic spectra and triplet state properties of superphane Chemical Physics. 110: 93-101. DOI: 10.1016/0301-0104(86)85147-3 |
0.332 |
|
| 1986 |
Hasselbach H, Krieger C, Decker M, Staab HA. Nicotinamide Coenzyme Models, II. Bis(methoxycarbonyl)‐N,N′‐dimethyl[2.2](2,5)pyridiniophane Diiodides: Preparation, Structure, and Reduction to Semi‐Reduced Systems European Journal of Organic Chemistry. 1986: 765-776. DOI: 10.1002/Jlac.198619860415 |
0.399 |
|
| 1986 |
Staab HA, Hasselbach H, Krieger C. Nicotinamide Coenzyme Models, I. Synthesis and Molecular Structure of Four Isomeric Bis(methoxycarbonyl)[2.2](2,5)pyridinophanes European Journal of Organic Chemistry. 1986: 751-764. DOI: 10.1002/Jlac.198619860414 |
0.382 |
|
| 1986 |
Saupe T, Krieger C, Staab HA. Novel "Proton Sponge" Compounds. Part 3. 4,5-Bis(dimethylamino)phenanthrene and 4,5-Bis(dimethylamino)-9,10-dihydrophenanthrene: Syntheses and "Proton Sponge" Properties. Cheminform. 17. DOI: 10.1002/Chin.198636061 |
0.349 |
|
| 1986 |
Hasselbach H-, Krieger C, Decker M, Staab HA. Nicotinamide Coenzyme Models. Part 2. Bis(methoxycarbonyl)-N,N′-dimethyl[2.2](2,5)pyridiniophane Diiodides: Preparation, Structure, and Reduction to Semi-Reduced Systems. Cheminform. 17. DOI: 10.1002/Chin.198632208 |
0.303 |
|
| 1986 |
Staab HA, Hasselbach H-, Krieger C. Nicotinamide Coenzyme Models. Part 1. Synthesis and Molecular Structure of Four Isomeric Bis(methoxycarbonyl)[2.2](2,5)pyridinophanes. Cheminform. 17. DOI: 10.1002/Chin.198632207 |
0.314 |
|
| 1986 |
Bauer H, Briaire J, Staab HA. Electron Donor‐Acceptor Compounds. Part 41. Cation‐Induced Charge‐Transfer Absorptions of Oligooxa[n.n]paracyclophane Quinhydrones (I). Cheminform. 17. DOI: 10.1002/Chin.198614235 |
0.31 |
|
| 1986 |
Elbl K, Krieger C, Staab HA. 1,2,4,5‐Tetrakis(dimethylamino)benzene, a New Electron Donor with Unusual Properties Angewandte Chemie. 25: 1023-1024. DOI: 10.1002/Anie.198610231 |
0.319 |
|
| 1986 |
Saupe T, Krieger C, Staab HA. 4,5‐Bis(dimethylamino)phenanthrene and 4,5‐Bis(dimethylamino)‐9,10‐dihydrophenanthrene: Syntheses and “Proton Sponge” Properties Angewandte Chemie. 25: 451-453. DOI: 10.1002/Anie.198604511 |
0.32 |
|
| 1986 |
Saupe T, Krieger C, Staab HA. 4,5‐Bis(dimethylamino)phenanthren und 4,5‐Bis(dimethylamino)‐9,10‐dihydrophenanthren: Synthesen und „Protonenschwamm”︁‐Eigenschaften Angewandte Chemie. 98: 460-462. DOI: 10.1002/Ange.19860980521 |
0.345 |
|
| 1985 |
Staab HA, Hasselbach HJ. Bis(methoxycarbonyl)[2.2](2,5)pyridinophanes as nicotinamide coenzyme models Tetrahedron Letters. 26: 5979-5982. DOI: 10.1016/S0040-4039(00)98276-5 |
0.3 |
|
| 1985 |
Weiser J, Staab HA. A new benzoquinone-bridged porphyrin Tetrahedron Letters. 26: 6059-6062. DOI: 10.1016/S0040-4039(00)95124-4 |
0.357 |
|
| 1985 |
Krieger C, Weiser J, Staab HA. Molecular structure and fluorescence behaviour of a benzoquinone/porphyrin/benzoquinone sandwich-molecule Tetrahedron Letters. 26: 6055-6058. DOI: 10.1016/S0040-4039(00)95123-2 |
0.345 |
|
| 1985 |
Butler Ransohoff JE, Staab HA. En route to hexaaza-kekulene Tetrahedron Letters. 26: 6179-6182. DOI: 10.1016/S0040-4039(00)95046-9 |
0.32 |
|
| 1985 |
Bauer H, Briaire J, Staab HA. Cation-induced charge-transfer absorptions of oligooxa[n.n]Paracyclophane quinhydrones Tetrahedron Letters. 26: 6175-6178. DOI: 10.1016/S0040-4039(00)95045-7 |
0.324 |
|
| 1985 |
Rosenau B, Krieger C, Staab HA. Sterically crowded tetracyano-para-quinodimethanes: synthesis and structure of 2,3,5,6-tetramethyl-7,7,8,8-tetracyano-para-quino=dimethane Tetrahedron Letters. 26: 2081-2084. DOI: 10.1016/S0040-4039(00)94784-1 |
0.321 |
|
| 1985 |
Vogler H, Schanne L, Staab HA. Electron Donor-Acceptor Compounds. Xl. Theoretical Explanation Of Charge-Transfer Absorptions Of Syn- And Anti-Donor Acceptor Metacyclophanes Cheminform. 16. DOI: 10.1002/Chin.198530186 |
0.337 |
|
| 1985 |
Staab HA, Reibel WRK, Krieger C. Electron Donor-Acceptor Compounds. Xxxix. Quinones And Quinhydrones Of The (2.2)Metacyclophane Series Cheminform. 16. DOI: 10.1002/Chin.198530185 |
0.337 |
|
| 1985 |
Staab HA, Schanne L, Krieger C, Taglieber V. Electron Donor-Acceptor Compounds. Xxxviii. Electron Donor-Acceptor (2.2)Metacyclophanes: Synthesis, Structure, And Charge-Transfer Spectra Cheminform. 16. DOI: 10.1002/Chin.198530184 |
0.37 |
|
| 1985 |
Staab HA, Joerns M, Krieger C, Rentzea M. Electron Donor-Acceptor Compounds, Xxxvi. Quinones And Quinhydrones Of The (2.2)- And (3.3)Metaparacyclophane Series Cheminform. 16. DOI: 10.1002/Chin.198526050 |
0.336 |
|
| 1985 |
Vogler H, Schanne L, Staab HA. Elektron-Donor-Acceptor-Verbindungen. XL: Theoretische Deutung der Charge-Transfer-Absorptionen von syn- und anti-Donor-Acceptor-Metacyclophanen Chemische Berichte. 118: 1254-1260. DOI: 10.1002/Cber.19851180338 |
0.323 |
|
| 1985 |
Staab HA, Reibel WRK, Kreiger C. Elektron-Donor-Acceptor-Verbindungen, XXXIX. Chinone und Chinhydrone der [2.2]Metacyclophan-Reihe Chemische Berichte. 118: 1230-1253. DOI: 10.1002/Cber.19851180337 |
0.37 |
|
| 1985 |
Staab HA, Schanne L, Krieger C, Taglieber VK. Elektron‐Donor‐Acceptor‐Verbindungen, XXXVIII. Elektron‐Donor‐Acceptor‐[2.2]Metacyclophane: Synthese, Struktur und Charge‐Transfer‐Spektren Chemische Berichte. 118: 1204-1229. DOI: 10.1002/Cber.19851180336 |
0.434 |
|
| 1985 |
Staab HA, Jörns M, Krieger C, Rentzea M. Electron donor-acceptor compounds. XXXVI: Quinones and quinhydrones of the [2.2] and [3.3]metaparacyclophane series Chemische Berichte. 118: 796-813. DOI: 10.1002/Cber.19851180238 |
0.397 |
|
| 1985 |
Koray AR, Krieger C, Staab HA. Bis(tricarbonyliron)‐para‐quinodimethanes: Preparation and Molecular Structure Angewandte Chemie. 24: 521-522. DOI: 10.1002/Anie.198505211 |
0.32 |
|
| 1985 |
Koray AR, Krieger C, Staab HA. Bis(tricarbonyleisen)-para-chinodimethane: Darstellung und Molekülstruktur Angewandte Chemie. 97: 513-514. DOI: 10.1002/Ange.19850970621 |
0.347 |
|
| 1984 |
Schanne L, Staab HA. Complexation of electron donor-acceptor [2.2] paracyclophanes with tetracyanoethylene (TCNE) Tetrahedron Letters. 25: 1721-1724. DOI: 10.1016/S0040-4039(01)81154-0 |
0.326 |
|
| 1984 |
Zipplies MF, Staab HA. π...π-interactions of flavins,-II. [3.3](3,10)Isoalloxazinophane and quinhydrone-like flavin interactions Tetrahedron Letters. 25: 1035-1038. DOI: 10.1016/S0040-4039(01)80093-9 |
0.344 |
|
| 1984 |
Alt R, Staab HA, Reisenauer HP, Maier G. Diarylcarbenes of unusual steric and electronic structure Tetrahedron Letters. 25: 633-636. DOI: 10.1016/S0040-4039(00)99957-X |
0.326 |
|
| 1984 |
Sauer M, Staab HA. [2.2](2,7)Anthracenophan: Synthese und Konformations‐Untersuchungen European Journal of Organic Chemistry. 1984: 615-617. DOI: 10.1002/Jlac.198419840320 |
0.325 |
|
| 1984 |
Gleiter R, Schäfer W, Staab HA, Saupe T. Electronic structure of 4,5-bis(dimethylamino)fluorene. PE spectroscopic investigations Journal of Organic Chemistry. 49: 4463-4465. DOI: 10.1002/Chin.198515086 |
0.331 |
|
| 1984 |
Diederich F, Schneider K, Staab HA. Dibenz(A,J)Anthracene Via Photo‐Cyclodehydrogenation Of 9,10‐Dihydro‐2‐Styrylphenanthrene Cheminform. 15. DOI: 10.1002/Chin.198423208 |
0.497 |
|
| 1984 |
Wahl P, Krieger C, Schweitzer D, Staab HA. 1,8‐Dipyrenylnaphthalenes: Syntheses, Molecular Structure, And Spectroscopic Properties Cheminform. 15. DOI: 10.1002/Chin.198412066 |
0.34 |
|
| 1984 |
STAAB HA, RIEGLER N, DIEDERICH F, KRIEGER C, SCHWEITZER D. ChemInform Abstract: (3.3)- AND (4.4)(2,7)PYRENOPHANES AS EXCIMER MODELS: SYNTHESIS, MOLECULAR STRUCTURE, AND SPECTROSCOPIC PROPERTIES Chemischer Informationsdienst. 15. DOI: 10.1002/Chin.198412065 |
0.563 |
|
| 1984 |
Diederich FN, Schneider K, Staab HA. Dibenz[a,j]anthracene via Photo‐cyclodehydrogenation of 9,10‐Dihydro‐2‐styrylphenanthrene Chemische Berichte. 117: 1255-1258. DOI: 10.1002/Cber.19841170339 |
0.528 |
|
| 1984 |
Wahl P, Krieger C, Schweitzer D, Staab HA. 1,8‐Dipyrenylnaphthalenes: Syntheses, Molecular Structure, and Spectroscopic Properties Chemische Berichte. 117: 260-276. DOI: 10.1002/Cber.19841170120 |
0.396 |
|
| 1984 |
Staab HA, Riegler N, Diederich F, Krieger C, Schweitzer D. [3.3]- and [4.4](2,7)Pyrenophanes as Excimer Models: Synthesis, Molecular Structure, and Spectroscopic Properties Chemische Berichte. 117: 246-259. DOI: 10.1002/Cber.19841170119 |
0.603 |
|
| 1983 |
Zipplies MF, Krieger C, Staab HA. π...π-interactions of flavins: Synthesis and molecular structure of a flavinocyclophane Tetrahedron Letters. 24: 1925-1928. DOI: 10.1016/S0040-4039(00)81807-9 |
0.336 |
|
| 1983 |
Staab HA, Diederich F, Čaplar V. Cycloarenes, a New Class of Aromatic Compounds, III. Studies towards the Synthesis of Cyclo[d.e.d.e.e.d.e.d.e.e]decakisbenzene Liebigs Annalen Der Chemie. 1983: 2262-2273. DOI: 10.1002/Jlac.198319831219 |
0.553 |
|
| 1983 |
STAAB HA, DIEDERICH F, KRIEGER C, SCHWEITZER D. ChemInform Abstract: CYCLOARENES, A NEW CLASS OF AROMATIC COMPOUNDS. II. MOLECULAR STRUCTURE AND SPECTROSCOPIC PROPERTIES OF KEKULENE Chemischer Informationsdienst. 14. DOI: 10.1002/Chin.198352057 |
0.559 |
|
| 1983 |
Staab HA, Hinz R, Knaus GH, Krieger C. Electron Donor‐Acceptor Compounds. Xxxii. An Electron Donor‐Acceptor Paracyclophane With N,N,N′,N′‐Tetramethyl‐P‐Phenylenediamine And 7,7,8,8‐Tetracyanoquinodimethane Subunits Cheminform. 14. DOI: 10.1002/Chin.198349174 |
0.306 |
|
| 1983 |
Staab HA, Knaus GH, Henke H-, Krieger C. Electron Donor-Acceptor Compounds. Xxix. Electron Donor-Acceptor Paracyclophanes With 7,7,8,8-Tetracyanoquinodimethane (Tcnq) As Acceptor Unit Cheminform. 14. DOI: 10.1002/Chin.198349171 |
0.329 |
|
| 1983 |
Bauer H, Briaire J, Staab HA. Electron Donor-Acceptor Compounds. Part 34. Cationically Controlled Charge-Transfer Absorption Of Intramolecular Quinhydrones With Oligooxaparacyclophane Structure Cheminform. 14. DOI: 10.1002/Chin.198328040 |
0.361 |
|
| 1983 |
Staab HA, Starker B, Krieger C. Elektron‐Donor‐Acceptor‐Verbindungen, XXXIV. Höhere [n.n]Paracyclophan‐Chinhydrone: Synthese, Molekülstruktur und spektroskopische Eigenschaften Chemische Berichte. 116: 3831-3845. DOI: 10.1002/Cber.19831161207 |
0.386 |
|
| 1983 |
Staab HA, Herz CP, Krieger C, Rentea M. Elektron‐Donor‐Acceptor‐Verbindungen, XXXIII. Intramolekulare Chinhydrone der [3.3]Paracyclophan‐Reihe Chemische Berichte. 116: 3813-3830. DOI: 10.1002/Cber.19831161206 |
0.436 |
|
| 1983 |
Staab HA, Diederich F, Krieger C, Schweitzer D. Cycloarenes, a New Class of Aromatic Compounds, II. Molecular Structure and Spectroscopic Properties of Kekulene Chemische Berichte. 116: 3504-3512. DOI: 10.1002/Cber.19831161022 |
0.598 |
|
| 1983 |
Staab HA, Diederich F. Cycloarenes, a New Class of Aromatic Compounds, I. Synthesis of Kekulene Chemische Berichte. 116: 3487-3503. DOI: 10.1002/Cber.19831161021 |
0.541 |
|
| 1983 |
Staab HA, Hinz R, Knaus GH, Krieger C. Elektron‐Donor‐Acceptor‐Verbindungen, XXXII. Ein Elektron‐Donor‐Acceptor‐Paracyclophan mit N,N,N′,N′‐Tetramethyl‐p‐phenylendiamin‐ und 7,7,8,8‐Tetracyanchinodimethan‐Untereinheiten Chemische Berichte. 116: 2835-2847. DOI: 10.1002/Cber.19831160810 |
0.422 |
|
| 1983 |
Staab HA, Gabel G, Krieger C. Elektron‐Donor‐Acceptor‐Verbindungen, XXXI. Elektron‐Donor‐Acceptor‐[3.3]Paracyclophane mit N,N,N′,N′‐Tetramethyl‐p‐phenylendiamin (TMPD) als Donor‐Einheit Chemische Berichte. 116: 2827-2834. DOI: 10.1002/Cber.19831160809 |
0.352 |
|
| 1983 |
Staab HA, Knaus GH, Henke H, Krieger C. Elektron‐Donor‐Acceptor‐Verbindungen, XXIX. Elektron‐Donor‐Acceptor‐Paracyclophane mit 7,7,8,8‐Tetracyanchinodimethan (TCNQ) als Acceptor‐Einheit Chemische Berichte. 116: 2785-2807. DOI: 10.1002/Cber.19831160807 |
0.434 |
|
| 1982 |
Schweitzer D, Hausser KH, Vogler H, Diederich F, Staab HA. Electronic properties of kekulene Molecular Physics. 46: 1141-1153. DOI: 10.1080/00268978200101861 |
0.512 |
|
| 1982 |
Staab HA, Kuo‐chen C, Ruland A. Triarylmethyl‐Systeme, IV. Synthese und Reaktionen von α‐Hydroxy‐ und α‐Halogen‐α‐aryl[1.n]paracyclophanen Chemische Berichte. 115: 1765-1774. DOI: 10.1002/Cber.19821150511 |
0.304 |
|
| 1981 |
Staab HA, Appel WK. Elektron-Donor-Acceptor-Verbindungen, XXVIII Synthese und Charge-Transfer-Eigenschaften von 4,7-Diaza[2.2]paracyclophanen European Journal of Organic Chemistry. 1981: 1065-1072. DOI: 10.1002/Jlac.198119810612 |
0.378 |
|
| 1981 |
Staab HA, Döhling A, Krieger C. Elektron‐Donor‐Acceptor‐Verbindungen, XXVII Chinhydrone der [4.4]Paracyclophan‐Reihe European Journal of Organic Chemistry. 1981: 1052-1064. DOI: 10.1002/Jlac.198119810611 |
0.397 |
|
| 1981 |
Staab HA, Doehling A, Krieger C. Electron Donor-Acceptor Compounds. Xxvii. Quinhydrones Of The (4.4)Paracyclophane Series Cheminform. 12. DOI: 10.1002/Chin.198138172 |
0.336 |
|
| 1980 |
Ippen J, Tao‐Pen C, Starker B, Schweitzer D, Staab HA. Electron Donor‐Acceptor Compounds. 26. (2.2)‐ And (3.3)Tetrathiafulvalenophanes Cheminform. 11. DOI: 10.1002/Chin.198016180 |
0.308 |
|
| 1980 |
Staab HA, Ippen J, Tao-Pen C, Krieger C, Starker B. Electron Donor-Acceptor Compounds. 25. Tetrathiafulvalenoparacyclophanes Cheminform. 11. DOI: 10.1002/Chin.198016179 |
0.328 |
|
| 1980 |
Staab HA, Herz CP, Doehling A+, Krieger C. Electron Donor-Acceptor Compounds. Xx. Intramolecular Quinhydrones Of The (3.3)Metacyclophane Series: Synthesis, Structure, Stability, And Charge-Transfer Absorptions Of Stereoisomeric(3.3)Metacyclophane Quinhydrones Cheminform. 11. DOI: 10.1002/Chin.198014221 |
0.378 |
|
| 1980 |
Staab HA, Herz CP, Doehling A. Electron Donor-Acceptor Compounds. Xix. Intramolecular Quinhydrones Of The (3.3)Metacyclophane Series: Syn- And Anti-6,9,15,18-Tetramethoxy(3.3)Metacyclophanes As Precursors Cheminform. 11. DOI: 10.1002/Chin.198014220 |
0.344 |
|
| 1980 |
Staab HA, Herz CP, Döhling A, Krieger C. Elektron‐Donor‐Acceptor‐Verbindungen, XX. Intramolekulare Chinhydrone der [3.3]Metacyclophan‐Reihe: Synthese, Struktur, Stabilität und Charge‐Transfer‐Absorptionen von stereoisomeren [3.3]Metacyclophan‐Chinhydronen Chemische Berichte. 113: 241-254. DOI: 10.1002/Cber.19801130125 |
0.386 |
|
| 1980 |
Staab HA, Herz CP, Döhling A. Elektron‐Donor‐Acceptor‐Verbindungen, XIX. Intramolekulare Chinhydrone der [3.3]Metacyclophan‐Reihe: syn‐ und anti‐6,9,15,18‐Tetramethoxy[3.3]metacyclophane als Vorstufen Chemische Berichte. 113: 233-240. DOI: 10.1002/Cber.19801130124 |
0.378 |
|
| 1980 |
Ippen J, Tao‐pen C, Starker B, Schweitzer D, Staab HA. [2.2]‐ und [3.3]Tetrathiafulvalenophane Angewandte Chemie. 92: 51-52. DOI: 10.1002/Ange.19800920114 |
0.306 |
|
| 1979 |
Staab HA, Knaus GH. The two diastereomers of [3] (2,5) (7,7,8,8-tetracyanoquinodimethano) - [3] (2,5-dimethoxyparacyclophane) Tetrahedron Letters. 20: 4261-4264. DOI: 10.1016/S0040-4039(01)86561-8 |
0.313 |
|
| 1979 |
Staab HA, Jörns M, Krieger C. Isomeric [2.2]metaparacyclophane quinhydrones Tetrahedron Letters. 20: 2513-2516. DOI: 10.1016/S0040-4039(01)86336-X |
0.339 |
|
| 1979 |
Staab HA, Döhling A. Anti-[3.3]metacyclophane quinhydrones: synthesis, charge-transfer absorption and thermal rearrangement to syn-stereoisomers Tetrahedron Letters. 20: 2019-2022. DOI: 10.1016/S0040-4039(01)86252-3 |
0.317 |
|
| 1979 |
KRIEGER C, DIEDERICH F, SCHWEITZER D, STAAB HA. ChemInform Abstract: CONJUGATION IN MACROCYCLIC BOND SYSTEMS. 30. MOLECULAR STRUCTURE AND SPECTROSCOPIC PROPERTIES OF KEKULENE Chemischer Informationsdienst. 10. DOI: 10.1002/Chin.197951204 |
0.558 |
|
| 1979 |
Staab HA, Meissner UE, Gensler A. Konjugation in makrocyclischen Bindungssystemen, XXIX. Synthese und Eigenschaften von Benzo[18]annulen Chemische Berichte. 112: 3907-3913. DOI: 10.1002/Cber.19791121215 |
0.374 |
|
| 1979 |
Staab HA, Meissner UE, Weinacht W, Gensler A. Konjugation in makrocyclischen Bindungssystemen, XXVIII. Benzo‐anellierte [14]Annulene Chemische Berichte. 112: 3895-3906. DOI: 10.1002/Cber.19791121214 |
0.375 |
|
| 1979 |
Krieger C, Diederich F, Schweitzer D, Staab HA. Molecular Structure and Spectroscopic Properties of Kekulene Angewandte Chemie International Edition in English. 18: 699-701. DOI: 10.1002/Anie.197906991 |
0.56 |
|
| 1979 |
Krieger C, Diederich F, Schweitzer D, Staab HA. Molekülstruktur und spektroskopische Eigenschaften des Kekulens Angewandte Chemie. 91: 733-735. DOI: 10.1002/Ange.19790910908 |
0.55 |
|
| 1978 |
Reimann R, Staab HA. Attempts to Synthesize Zwitterionic Donor‐Acceptor Cyclophanes: The Diastereomeric 12,15‐Bis(dimethylamino)‐[2](2,5)‐p‐benzoquinono[2]paracyclophanes Angewandte Chemie. 17: 374-375. DOI: 10.1002/Anie.197803741 |
0.365 |
|
| 1978 |
Diederich F, Staab HA. Benzenoidversus Annulenoid Aromaticity: Synthesis and Properties of Kekulene Angewandte Chemie International Edition in English. 17: 372-374. DOI: 10.1002/Anie.197803721 |
0.548 |
|
| 1978 |
Staab HA, Zapf U. Indirekte Donor‐Acceptor‐Wechselwirkungen bei Chinhydronen vierschichtiger [2.2]Paracyclophane Angewandte Chemie. 90: 807-808. DOI: 10.1002/Ange.19780901017 |
0.319 |
|
| 1978 |
Diederich F, Staab HA. Benzoide versus annulenoide Aromatizität: Synthese und Eigenschaften des Kekulens Angewandte Chemie. 90: 383-385. DOI: 10.1002/Ange.19780900513 |
0.567 |
|
| 1977 |
Haenel MW, Flatow A, Taglieber V, Staab HA. Orientation Effects On Charge-Transfer-Interactions. Part 10. New Syntheses Of (3.3)Paracyclophanes. Diastereomeric Donor-Acceptor-(3.3)Paracyclophanes Cheminform. 8. DOI: 10.1002/Chin.197734206 |
0.315 |
|
| 1977 |
Herz CP, Staab HA. An Intramolecular Quinhydrone of the [2](1,4)Naphthaleno[2]paracyclophane Series Angewandte Chemie. 16: 394-394. DOI: 10.1002/Anie.197703941 |
0.318 |
|
| 1977 |
Herz CP, Staab HA. Ein intramolekulares Chinhydron der [2](1,4)Naphthalion[2]paracyclophan‐Reihe Angewandte Chemie. 89: 407-408. DOI: 10.1002/Ange.19770890609 |
0.302 |
|
| 1976 |
Schweitzer D, Hausser KH, Taglieber V, Staab HA. Electronic properties of two isomeric charge transfer [2.2]paracyclophanes Chemical Physics. 14: 183-187. DOI: 10.1016/0301-0104(76)80037-7 |
0.304 |
|
| 1975 |
Schweitzer D, Colpa JP, Behnke J, Hausser KH, Haenel M, Staab HA. Transannular interactions in [2,2] phanes as studied by magnetic resonance and optical spectra Chemical Physics. 11: 373-384. DOI: 10.1016/0301-0104(75)80056-5 |
0.32 |
|
| 1974 |
Irngartinger H, Acker R, Rebafka W, Staab HA. Transannulare Wechselwirkungen Bei (2.2)Phanen 7. Mitt. (2,2)(2,5)Benzochinonophane, Struktur Und Photochemie Cheminform. 5. DOI: 10.1002/Chin.197451160 |
0.312 |
|
| 1974 |
Irngartinger H, Acker R, Rebafka W, Staab HA. [2.2](2,5)Benzochinonophane: Struktur und Photochemie Angewandte Chemie. 86: 705-706. DOI: 10.1002/Ange.19740861908 |
0.31 |
|
| 1973 |
Meissner U, Meissner B, Staab HA. Konjugation In Makrocyclischen Bindungssystemen 21. Mitt. Cyclooctadeca(Cdefg)Phenanthren (′(18)Annuleno(Cdefg)Phenanthren′) Cheminform. 4. DOI: 10.1002/Chin.197352292 |
0.313 |
|
| 1973 |
Haenel M, Staab HA. Transannulare Wechselwirkungen Bei (2,2)Phanen 3. Mitt. (2,2)(2,6)Naphthalinophan Und (2,2)(2,6)Naphthalinophan-1,11-Dien Cheminform. 4. DOI: 10.1002/Chin.197336243 |
0.342 |
|
| 1973 |
Staab HA, Haenel M. Transannulare Wechselwirkungen Bei (2,2)Phanen 2. Mitt. Synth. Von (2,2)(4,4′)Biphenylophan, (2,2)(2,7)Phenanthrenophan Und (2)(4,4′)Biphenylo(2)(2,7)Phenanthrenophan Cheminform. 4. DOI: 10.1002/Chin.197336240 |
0.302 |
|
| 1973 |
Rebafka W, Staab HA. Ein „intramolekulares Chinhydron”︁ Angewandte Chemie. 85: 831-832. DOI: 10.1002/Ange.19730851818 |
0.307 |
|
| 1972 |
Staab HA, Draeger B. Intramolekulare Wechselwirkungen Zwischen Dreifachbindungen 13. Mitt. 1,2‐Bis‐(3‐Phenyl‐Propin‐(2)‐Yl)‐Benzol Und Verwandte Verbindungen Cheminform. 3. DOI: 10.1002/Chin.197236246 |
0.31 |
|
| 1971 |
Meissner B, Staab HA. Sterisch behinderte Diarylborane: 1H-NMR-Untersuchungen zur Rotation um Kohlenstoff-Bor-Bindungen European Journal of Organic Chemistry. 753: 92-99. DOI: 10.1002/Jlac.19717530108 |
0.305 |
|
| 1970 |
Haenel M, Staab HA. Synthese von [2.2]cyclophanen: [2.2]-(4.4′)-biphenylophan, [2.2]-(2.6)-naphthalinophan und [2.2]-(2.7)-phenanthrenophan Tetrahedron Letters. 11: 3585-3588. DOI: 10.1016/S0040-4039(01)98534-X |
0.358 |
|
| 1969 |
Binnig F, Meyer H, Staab HA. Zur Konjugation in makrocyclischen Bindungssystemen, XIII1) Weitere Verbindungen des Hexa‐m‐phenylen‐Typs European Journal of Organic Chemistry. 724: 24-29. DOI: 10.1002/Jlac.19697240104 |
0.352 |
|
| 1965 |
Staab HA, Vögtle F, Mannschreck A. Untersuchungen über schiff'sche basen IV: rotonenresonanz-untersuchungen zur syn-anti-isomerie bei schiff'schen basen Tetrahedron Letters. 6: 697-702. |
0.433 |
|
| 1964 |
Staab HA, Wu MT, Mannschreck A, Schwalbach G. H/D-austausch bei azolen und azolium-salzen Tetrahedron Letters. 5: 845-848. DOI: 10.1016/S0040-4039(00)90393-9 |
0.441 |
|
| 1963 |
Mannschreck A, Staab HA, Wurmb-Gerlich D. Protonenresonanz-untersuchungen zur inneren rotation I: behinderte rotation um einfachbindungen bei mesitoyl-verbindungen Tetrahedron Letters. 4: 2003-2008. DOI: 10.1016/S0040-4039(01)90959-1 |
0.402 |
|
| 1962 |
Staab HA, Mannschreck A. Protonenresonanz und protonenaustausch bei diazolen Tetrahedron Letters. 3: 913-916. DOI: 10.1016/S0040-4039(00)70564-8 |
0.495 |
|
| 1959 |
Staab HA. Reaktionsfähige heterocyclische Amide der Kohlensäure, V Zur Reaktionsfähigkeit von N-Acyl-pyrazolen European Journal of Organic Chemistry. 622: 31-36. DOI: 10.1002/Jlac.19596220106 |
0.327 |
|
| 1959 |
Staab HA, Seel G. Transacylierungen, V. Über N-Acyl-Derivate des 3-Amino-1.2.4-triazols Chemische Berichte. 92: 1302-1306. DOI: 10.1002/Cber.19590920611 |
0.316 |
|
| 1958 |
Staab HA. Hundert Jahre organische Strukturchemie Angewandte Chemie. 70: 37-41. DOI: 10.1002/Ange.19580700202 |
0.315 |
|
| 1957 |
Staab HA. Reaktionsfähige N-Carbonsäureester und N-Carbonsäureamide des Imidazols und Triazols European Journal of Organic Chemistry. 609: 83-88. DOI: 10.1002/Jlac.19576090109 |
0.317 |
|
| 1957 |
Staab HA. Reaktionsfähige Heterocyclische Diamide der Kohlensäure European Journal of Organic Chemistry. 609: 75-83. DOI: 10.1002/Jlac.19576090108 |
0.323 |
|
| 1957 |
Staab HA. Transacylierungen, IV. Reaktionsfähige Heterocyclische Amide von Dicarbonsäuren Chemische Berichte. 90: 1326-1330. DOI: 10.1002/Cber.19570900727 |
0.359 |
|
| 1957 |
Staab HA. Transacylierungen, III. Über Die Reaktionsfähigkeit der N‐Acyl‐Derivate in der Reihe Indol/Benzimidazol/Benztriazol Chemische Berichte. 90: 1320-1325. DOI: 10.1002/Cber.19570900726 |
0.366 |
|
| 1954 |
Kuhn R, Staab HA. Über den 2.4-Dioxy-isophthalaldehyd Chemische Berichte. 87: 272-275. DOI: 10.1002/Cber.19540870223 |
0.481 |
|
| 1954 |
Kuhn R, Staab HA. Synthese Kernsubstituierter Sorbophenone Chemische Berichte. 87: 266-272. DOI: 10.1002/Cber.19540870222 |
0.495 |
|
| 1954 |
Kuhn R, Staab HA. Synthese von Polyenylphenyl‐ketonen Chemische Berichte. 87: 262-266. DOI: 10.1002/Cber.19540870221 |
0.543 |
|
| 1953 |
Kuhn R, Inhoffen HH, Staab HA, Otting W. Vergleich des cis‐Crocetin‐dimethylesters aus Safran mit 8.8′‐cis‐Crocetin‐dimethylester Chemische Berichte. 86: 965-968. DOI: 10.1002/Cber.19530860808 |
0.456 |
|
| 1953 |
Kuhn R, Staab HA. Synthese des Sorbophenons und Sorbicillins Angewandte Chemie. 65: 371-371. DOI: 10.1002/Ange.19530651405 |
0.503 |
|
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