| Year |
Citation |
Score |
| 2018 |
Kharkwal SS, Veerapen N, Jervis P, Bhowruth V, Besra AK, North SJ, Haslam SM, Dell A, Hobrath J, Quaid P, Moynihan P, Cox LR, Kharkwal H, Zauderer M, Besra GS, et al. Photoactivable glycolipid antigens generate stable conjugates with CD1d for invariant Natural Killer T cell activation. Bioconjugate Chemistry. PMID 30085659 DOI: 10.1021/Acs.Bioconjchem.8B00484 |
0.354 |
|
| 2016 |
Jukes JP, Gileadi U, Ghadbane H, Yu TF, Shepherd D, Cox LR, Besra GS, Cerundolo V. Non-glycosidic compounds can stimulate both human and mouse iNKT cells. European Journal of Immunology. PMID 26873393 DOI: 10.1002/Eji.201546114 |
0.312 |
|
| 2015 |
Dossa RG, Alperin DC, Garzon D, Mealey RH, Brown WC, Jervis PJ, Besra GS, Cox LR, Hines SA. In contrast to other species, α-Galactosylceramide (α-GalCer) is not an immunostimulatory NKT cell agonist in horses. Developmental and Comparative Immunology. 49: 49-58. PMID 25445911 DOI: 10.1016/J.Dci.2014.11.005 |
0.307 |
|
| 2014 |
Cenci SM, Cox LR, Leeke GA. Ultrasound-Induced CO2/H2O Emulsions as a Medium for Clean Product Formation and Separation: The Barbier Reaction as a Synthetic Example Acs Sustainable Chemistry & Engineering. 2: 1280-1288. DOI: 10.1021/Sc500112Q |
0.347 |
|
| 2013 |
Jervis PJ, Polzella P, Wojno J, Jukes JP, Ghadbane H, Garcia Diaz YR, Besra GS, Cerundolo V, Cox LR. Design, synthesis, and functional activity of labeled CD1d glycolipid agonists. Bioconjugate Chemistry. 24: 586-94. PMID 23458425 DOI: 10.1021/Bc300556E |
0.338 |
|
| 2012 |
Jervis PJ, Graham LM, Foster EL, Cox LR, Porcelli SA, Besra GS. New CD1d agonists: synthesis and biological activity of 6″-triazole-substituted α-galactosyl ceramides. Bioorganic & Medicinal Chemistry Letters. 22: 4348-52. PMID 22652050 DOI: 10.1016/J.Bmcl.2012.05.009 |
0.317 |
|
| 2012 |
Jervis PJ, Moulis M, Jukes JP, Ghadbane H, Cox LR, Cerundolo V, Besra GS. Towards multivalent CD1d ligands: synthesis and biological activity of homodimeric α-galactosyl ceramide analogues. Carbohydrate Research. 356: 152-62. PMID 22445102 DOI: 10.1016/J.Carres.2012.02.034 |
0.383 |
|
| 2012 |
Wojno J, Jukes JP, Ghadbane H, Shepherd D, Besra GS, Cerundolo V, Cox LR. Amide analogues of CD1d agonists modulate iNKT-cell-mediated cytokine production. Acs Chemical Biology. 7: 847-55. PMID 22324848 DOI: 10.1021/Cb2005017 |
0.322 |
|
| 2011 |
Kaur R, Chen J, Dawoodji A, Cerundolo V, Garcia-Diaz YR, Wojno J, Cox LR, Besra GS, Moghaddam B, Perrie Y. Preparation, characterisation and entrapment of a non-glycosidic threitol ceramide into liposomes for presentation to invariant natural killer T cells. Journal of Pharmaceutical Sciences. 100: 2724-33. PMID 21283989 DOI: 10.1002/Jps.22500 |
0.303 |
|
| 2011 |
Jervis PJ, Cox LR, Besra GS. Synthesis of a versatile building block for the preparation of 6-N-derivatized α-galactosyl ceramides: rapid access to biologically active glycolipids. The Journal of Organic Chemistry. 76: 320-3. PMID 21155575 DOI: 10.1021/Jo102064P |
0.345 |
|
| 2010 |
Gleixner RM, Joly KM, Tremayne M, Kariuki BM, Male L, Coe DM, Cox LR. Reaction of 1,1'-divinyl ferrocene with one-electron oxidants: entry into functionalised [4]ferrocenophanes and observation of an isotope-dependent chemoselectivity effect. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 5769-77. PMID 20391576 DOI: 10.1002/Chem.200903478 |
0.349 |
|
| 2010 |
Ley SV, Burckhardt S, Cox LR, Worrall JM. ChemInform Abstract: Reductive Decomplexation of π-Allyltricarbonyliron Lactone Complexes: A New Route to Stereodefined Acyclic 1,5-Diols and 1,5,7-Triols. Cheminform. 31: no-no. DOI: 10.1002/chin.200019054 |
0.444 |
|
| 2010 |
Ley SV, Cox LR, Middleton B, Worrall JM. ChemInform Abstract: 1,7-Induction of Chirality in Mukaiyama Aldol Reactions Using π-Allyltricarbonyliron Lactone and Lactam Complexes as Chiral Templates Cheminform. 30: no-no. DOI: 10.1002/chin.199931028 |
0.488 |
|
| 2010 |
LEY SV, COX LR, WORRALL JM. ChemInform Abstract: Double Diastereodifferentiation in the Mukaiyama Aldol Reactions of π-Allyltricarbonyliron Lactone Complexes: 1,7- vs. 1,2-Asymmetric Induction. Cheminform. 30: no-no. DOI: 10.1002/chin.199908039 |
0.482 |
|
| 2010 |
COX LR, LEY SV. ChemInform Abstract: Tricarbonyliron Complexes: An Approach to Acyclic Stereocontrol Cheminform. 30: no-no. DOI: 10.1002/chin.199902297 |
0.372 |
|
| 2010 |
LEY SV, COX LR, MIDDLETON B, WORRALL JM. ChemInform Abstract: Mukaiyama Aldol Reactions of π-Allyltricarbonyliron Lactone and Lactam Complexes Bearing Trimethylsilyl Enol Ether Side-Chains. Not Just Formal, but Genuine 1,7-Induction of Chirality. Cheminform. 29: no-no. DOI: 10.1002/chin.199845184 |
0.509 |
|
| 2010 |
LEY SV, COX LR. ChemInform Abstract: Highly Diastereoselective Synthesis of β-Hydroxy Carbonyl Compounds Using π-Allyltricarbonyliron Lactone Complexes: A Formal 1,7-Asymmetric Induction of Chirality in a Mukaiyama Aldol Reaction. Cheminform. 29: no-no. DOI: 10.1002/chin.199820053 |
0.488 |
|
| 2010 |
LEY SV, BURCKHARDT S, COX LR, WORRALL JM. ChemInform Abstract: A Novel Decomplexation of π-Allyltricarbonyliron Lactone Complexes Using Borohydride Reagents: A New Route to Stereodefined Acyclic 1,5-Diols and 1,5,7-Triols. Cheminform. 29: no-no. DOI: 10.1002/chin.199819034 |
0.459 |
|
| 2010 |
LEY SV, COX LR. ChemInform Abstract: 1,5-Asymmetric Induction of Chirality: Highly Diastereoselective Synthesis of Homoallylic Tertiary Alcohols by the Lewis Acid-Mediated Addition of Allylstannanes into Ketones in the Side-Chain of π-Allyltricarbonyliron Lactone Complex Cheminform. 29: no-no. DOI: 10.1002/chin.199814038 |
0.482 |
|
| 2010 |
LEY SV, COX LR, MEEK G, METTEN K, PIQUE C, WORRALL JM. ChemInform Abstract: 1,5-Asymmetric Induction of Chirality: Highly Diastereoselective Addition Reactions of Organoaluminum Reagents into Ketone Groups in the Side-Chain of π-Allyltricarbonyliron Lactone Complexes. Cheminform. 29: no-no. DOI: 10.1002/chin.199814037 |
0.513 |
|
| 2010 |
LEY SV, BURCKHARDT S, COX LR, MEEK G. ChemInform Abstract: 1,5-Asymmetric Induction of Chirality: Diastereoselective Addition of Organoaluminum Reagents and Allylstannanes into Aldehyde Groups in the Side-Chain of π-Allyltricarbonyliron Lactone Complexes. Cheminform. 29: no-no. DOI: 10.1002/chin.199813040 |
0.482 |
|
| 2010 |
LEY SV, COX LR. ChemInform Abstract: Diastereoselective Addition Reactions of Allylstannanes to Carbonyl Groups in the Side-Chain of π-Allyltricarbonyliron Lactone Complexes. Cheminform. 27: no-no. DOI: 10.1002/chin.199629033 |
0.472 |
|
| 2010 |
LEY SV, COX LR, MEEK G. ChemInform Abstract: (π-Allyl)tricarbonyliron Lactone Complexes in Organic Synthesis: A Useful and Conceptually Unusual Route to Lactones and Lactams Cheminform. 27: no-no. DOI: 10.1002/chin.199622294 |
0.452 |
|
| 2009 |
Weller MD, Kariuki BM, Cox LR. Synthesis of hybrid masked triyne-phenylene axial rods containing (E)-beta-chlorovinylsilanes in the pi-conjugated framework. The Journal of Organic Chemistry. 74: 7898-907. PMID 19813769 DOI: 10.1021/Jo901766P |
0.37 |
|
| 2009 |
Diaz YRG, Wojno J, Cox LR, Besra GS. Synthesis of threitol ceramide and [14C]threitol ceramide, non-glycosidic analogues of the potent CD1d antigen α-galactosyl ceramide Tetrahedron-Asymmetry. 20: 747-753. DOI: 10.1016/J.Tetasy.2009.02.020 |
0.369 |
|
| 2009 |
Weller MD, Cox LR. A novel twist on an old theme: β-Halovinylsilanes, a new elimination approach to oligoyne assembly Comptes Rendus Chimie. 12: 366-377. DOI: 10.1016/J.Crci.2008.09.027 |
0.316 |
|
| 2008 |
Jervis PJ, Cox LR. Total synthesis and proof of relative stereochemistry of (-)-aureonitol. The Journal of Organic Chemistry. 73: 7616-24. PMID 18774862 DOI: 10.1021/Jo801338T |
0.371 |
|
| 2008 |
Beignet J, Jervis PJ, Cox LR. Temporary silicon connection strategies in intramolecular allylation of aldehydes with allylsilanes. The Journal of Organic Chemistry. 73: 5462-75. PMID 18557649 DOI: 10.1021/Jo800824X |
0.435 |
|
| 2008 |
Ramalho R, Jervis PJ, Kariuki BM, Humphries AC, Cox LR. A Brønsted acid mediated cascade enone synthesis from aldehydes containing a tethered propargylsilane Journal of Organic Chemistry. 73: 1631-1634. PMID 18197686 DOI: 10.1021/Jo702351S |
0.398 |
|
| 2008 |
Jervis PJ, Kariuki BM, Cox LR. Stereoselective synthesis of 3,4-disubstituted tetrahydrofurans and 2,3,4-trisubstituted tetrahydrofurans using an intramolecular allylation strategy employing allylsilanes Tetrahedron Letters. 49: 2514-2518. DOI: 10.1016/J.Tetlet.2008.02.088 |
0.395 |
|
| 2008 |
Jervis PJ, Kariuki BM, Cox LR. ChemInform Abstract: Stereoselective Synthesis of 3,4-Disubstituted Tetrahydrofurans and 2,3,4-Trisubstituted Tetrahydrofurans Using an Intramolecular Allylation Strategy Employing Allylsilanes. Cheminform. 39. DOI: 10.1002/CHIN.200831133 |
0.316 |
|
| 2007 |
Williams I, Reeves K, Kariuki BM, Cox LR. Stereoselective synthesis of 2-dienyl-substituted piperidines using an eta4-dienetricarbonyliron complex as the stereocontrolling element in a double reductive amination cascade. Organic & Biomolecular Chemistry. 5: 3325-9. PMID 17912386 DOI: 10.1039/B710898B |
0.49 |
|
| 2007 |
Jervis PJ, Cox LR. Tether-directed synthesis of highly substituted oxasilacycles via an intramolecular allylation employing allylsilanes. Beilstein Journal of Organic Chemistry. 3: 6. PMID 17288602 DOI: 10.1186/1860-5397-3-6 |
0.414 |
|
| 2007 |
Joly KM, Gleixner RM, Simpkins SME, Coe DM, Cox LR. Synthesis of (2-aminoethyl)ferrocenes from the reaction of lithium amides with vinylferrocene Tetrahedron. 63: 761-767. DOI: 10.1016/J.Tet.2006.10.078 |
0.428 |
|
| 2006 |
Jervis PJ, Kariuki BM, Cox LR. Stereoselective synthesis of 2,4,5-trisubstituted tetrahydropyrans using an intramolecular allylation strategy. Organic Letters. 8: 4649-52. PMID 16986972 DOI: 10.1021/Ol061957V |
0.44 |
|
| 2006 |
Williams I, Kariuki BM, Reeves K, Cox LR. Stereoselective synthesis of 2-dienyl-substituted pyrrolidines using an eta4-dienetricarbonyliron complex as the stereodirecting element: Elaboration to the pyrrolizidine skeleton. Organic Letters. 8: 4389-92. PMID 16986907 DOI: 10.1021/Ol061132L |
0.427 |
|
| 2006 |
Simpkins SME, Kariuki BM, Cox LR. Towards the synthesis of insulated oligoynes: A ring-closing-metathesis approach to molecular encapsulation Journal of Organometallic Chemistry. 691: 5517-5523. DOI: 10.1016/J.Jorganchem.2006.07.021 |
0.364 |
|
| 2005 |
Ramalho R, Beignet J, Humphries AC, Cox LR. Using a temporary silicon connection in a highly stereoselective synthesis of a new class of cyclic allenylsilanes Synthesis. 3389-3397. DOI: 10.1055/S-2005-918465 |
0.424 |
|
| 2005 |
Joly KM, Kariuki BM, Coe DM, Cox LR. One-pot synthesis of 1,1′-bis(2-amino)ethyl-substituted ferrocenes from the reaction of spiro[2.4]hepta-4,6-diene with lithium amides: An expedient route into functionalized ferrocenophanes Organometallics. 24: 358-366. DOI: 10.1021/Om049222M |
0.447 |
|
| 2005 |
Cox LR, DeBoos GA, Fullbrook JJ, Percy JM, Spencer N. Applying asymmetric dihydroxylation to the synthesis of difluorinated carbohydrate analogues: a 1,1-difluoro-1-deoxy-d-xylulose Tetrahedron-Asymmetry. 16: 347-359. DOI: 10.1016/J.Tetasy.2004.11.017 |
0.398 |
|
| 2004 |
Beignet J, Tiernan J, Woo CH, Kariuki BM, Cox LR. Stereoselective synthesis of allyl-C-mannosyl compounds: use of a temporary silicon connection in intramolecular allylation strategies with allylsilanes. The Journal of Organic Chemistry. 69: 6341-56. PMID 15357594 DOI: 10.1021/Jo049061W |
0.42 |
|
| 2004 |
Aricó CS, Cox LR. Regio- and stereoselective hydrosilylation of terminal alkynes using Grubbs' first-generation olefin-metathesis catalyst. Organic & Biomolecular Chemistry. 2: 2558-62. PMID 15351817 DOI: 10.1039/B409832C |
0.385 |
|
| 2004 |
Attrill R, Tye H, Cox LR. α-Amino acid synthesis via a Cu(II) chiral Lewis acid mediated addition of soft carbon nucleophiles to glycine cation equivalents Tetrahedron Asymmetry. 15: 1681-1684. DOI: 10.1016/J.Tetasy.2004.04.018 |
0.346 |
|
| 2003 |
Beignet J, Cox LR. Using a temporary silicon connection in stereoselective allylation with allylsilanes: application to the synthesis of stereodefined 1,2,4-triols. Organic Letters. 5: 4231-4. PMID 14572292 DOI: 10.1021/Ol035762O |
0.367 |
|
| 2003 |
Simpkins SM, Kariuki BM, Aricó CS, Cox LR. Stereoselective synthesis of beta-(chloro)vinylsilanes using a regio- and (E)-stereoselective bis-stannylation of unsymmetrically substituted butadiynes: application to the synthesis of a masked triyne. Organic Letters. 5: 3971-4. PMID 14535756 DOI: 10.1021/Ol035536E |
0.434 |
|
| 2003 |
Cox LR, DeBoos GA, Fullbrook JJ, Percy JM, Spencer NS, Tolley M. Catalytic asymmetric synthesis of a 1-deoxy-1,1-difluoro-D-xylulose. Organic Letters. 5: 337-9. PMID 12556186 DOI: 10.1021/Ol0273553 |
0.436 |
|
| 2002 |
Livingston R, Cox L, Odermatt S, Diederich F. 1,3-Diethynylallenes: Carbon-Rich Modules for Three-Dimensional Acetylenic Scaffolding Helvetica Chimica Acta. 85: 3052-3077. DOI: 10.1002/1522-2675(200210)85:10<3052::Aid-Hlca3052>3.0.Co;2-4 |
0.48 |
|
| 2001 |
Livingston RC, Cox LR, Gramlich V, Diederich F. 1,3-Diethynylallenes: New Modules for Three-Dimensional Acetylenic Scaffolding. Angewandte Chemie (International Ed. in English). 40: 2334-2337. PMID 29711830 DOI: 10.1002/1521-3773(20010618)40:12<2334::AID-ANIE2334>3.0.CO;2-7 |
0.396 |
|
| 2001 |
Livingston RC, Cox LR, Gramlich V, Diederich F. 1,3-diethynylallenes: New modules for three-dimensional acetylenic scaffolding Angewandte Chemie - International Edition. 40: 2334-2337. DOI: 10.1002/1521-3773(20010618)40:12<2334::Aid-Anie2334>3.0.Co;2-7 |
0.446 |
|
| 2001 |
Livingston RC, Cox LR, Gramlich V, Diederich F. 1,3-Diethynylallenes: New Modules for Three-Dimensional Acetylenic Scaffolding Angewandte Chemie. 113: 2396-2399. DOI: 10.1002/1521-3757(20010618)113:12<2396::aid-ange2396>3.0.co;2-k |
0.314 |
|
| 2000 |
Ley SV, Burckhardt S, Cox LR, Worrall JM. Reductive decomplexation of π-allyltricarbonyliron lactone complexes: a new route to stereodefined acyclic 1,5-diols and 1,5,7-triols Journal of the Chemical Society-Perkin Transactions 1. 211-217. DOI: 10.1039/A907630A |
0.479 |
|
| 1999 |
Ley SV, Cox LR, Middleton B, Worrall JM. 1,7-Induction of chirality in Mukaiyama aldol reactions using π- allyltricarbonyliron lactone and lactam complexes as chiral templates Tetrahedron. 55: 3515-3530. DOI: 10.1016/S0040-4020(98)01159-4 |
0.547 |
|
| 1998 |
Ley SV, Cox LR, Worrall JM. Double diastereodifferentiation in the Mukaiyama aldol reactions of π-allyltricarbonyliron lactone complexes: 1,7- vs. 1,2-asymmetric induction Journal of the Chemical Society-Perkin Transactions 1. 3349-3354. DOI: 10.1039/A805996I |
0.541 |
|
| 1997 |
Ley SV, Cox LR. 1,5-Asymmetric induction of chirality: highly diastereoselective synthesis of homoallylic tertiary alcohols by the Lewis acid-mediated addition of allylstannanes into ketones in the side-chain of π-allyltricarbonyliron lactone complexes Journal of the Chemical Society-Perkin Transactions 1. 3315-3326. DOI: 10.1039/A704491G |
0.552 |
|
| 1997 |
Ley SV, Burckhardt S, Cox LR, Meek G. 1,5-Asymmetric induction of chirality: diastereoselective addition of organoaluminium reagents and allylstannanes into aldehyde groups in the side-chain of π-allyltricarbonyliron lactone complexes Journal of the Chemical Society-Perkin Transactions 1. 3327-3338. DOI: 10.1039/A704487I |
0.562 |
|
| 1997 |
Ley SV, Cox LR, Meek G, Metten K, Piqué C, Worrall JM. 1,5-Asymmetric induction of chirality: highly diastereoselective addition reactions of organoaluminium reagents into ketone groups in the side-chain of π-allyltricarbonyliron lactone complexes Journal of the Chemical Society-Perkin Transactions 1. 3299-3314. DOI: 10.1039/A704481J |
0.569 |
|
| 1996 |
Ley SV, Cox LR, Meek G. (pi-Allyl)tricarbonyliron Lactone Complexes in Organic Synthesis: A Useful and Conceptually Unusual Route to Lactones and Lactams. Chemical Reviews. 96: 423-442. PMID 11848759 DOI: 10.1021/Cr950015T |
0.503 |
|
| 1996 |
Ley SV, Cox LR. Diastereoselective addition reactions of allylstannanes to carbonyl groups in the side-chain of π-allyltricarbonyliron lactone complexes Chemical Communications. 657-658. DOI: 10.1039/Cc9960000657 |
0.555 |
|
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