| Year |
Citation |
Score |
| 2021 |
Huters AD, Stambuli J, Klix RC, Matulenko MA, Chan VS, Simanis J, Hill DR, Reddy RE, Towne TB, Bellettini JR, Kotecki BJ, Cardinal-David B, Ji J, Voight EA, Shou M, et al. Scalable Asymmetric Syntheses of Foslevodopa and Foscarbidopa Drug Substances for the Treatment of Parkinson's Disease. The Journal of Organic Chemistry. PMID 34280307 DOI: 10.1021/acs.joc.1c00905 |
0.395 |
|
| 2013 |
Cardinal-David B, Scheidt KA. Carbene catalysis: Beyond the benzoin and stetter reactions Topics in Organometallic Chemistry. 44: 233-260. DOI: 10.1007/3418-2012-47 |
0.609 |
|
| 2011 |
Cohen DT, Cardinal-David B, Scheidt KA. Lewis acid activated synthesis of highly substituted cyclopentanes by the N-heterocyclic carbene catalyzed addition of homoenolate equivalents to unsaturated ketoesters. Angewandte Chemie (International Ed. in English). 50: 1678-82. PMID 21308931 DOI: 10.1002/Anie.201005908 |
0.742 |
|
| 2011 |
Cohen DT, Cardinal-David B, Roberts JM, Sarjeant AA, Scheidt KA. NHC-catalyzed/titanium(IV)-mediated highly diastereo- and enantioselective dimerization of enals. Organic Letters. 13: 1068-71. PMID 21271734 DOI: 10.1021/Ol103112V |
0.682 |
|
| 2011 |
Cohen DT, Cardinal-David B, Roberts JM, Sarjeant AA, Scheidt KA. Titanium-Mediated Diastereo- and Enantioselective Dimerizationof Enals Synfacts. 2011: 665-665. DOI: 10.1055/S-0030-1260366 |
0.667 |
|
| 2011 |
Cohen DT, Cardinal-David B, Scheidt KA. NHC-Catalyzed Addition of Homoenolate Equivalents to UnsaturatedKeto Esters Synfacts. 2011: 437-437. DOI: 10.1055/S-0030-1259613 |
0.716 |
|
| 2011 |
Cohen DT, Cardinal-David B, Scheidt KA. Innentitelbild: Lewis Acid Activated Synthesis of Highly Substituted Cyclopentanes by the N-Heterocyclic Carbene Catalyzed Addition of Homoenolate Equivalents to Unsaturated Ketoesters (Angew. Chem. 7/2011) Angewandte Chemie. 123: 1484-1484. DOI: 10.1002/Ange.201007985 |
0.708 |
|
| 2010 |
Raup DE, Cardinal-David B, Holte D, Scheidt KA. Cooperative catalysis by carbenes and Lewis acids in a highly stereoselective route to gamma-lactams. Nature Chemistry. 2: 766-71. PMID 20729898 DOI: 10.1038/Nchem.727 |
0.729 |
|
| 2010 |
Cardinal-David B, Raup DE, Scheidt KA. Cooperative N-heterocyclic carbene/Lewis acid catalysis for highly stereoselective annulation reactions with homoenolates. Journal of the American Chemical Society. 132: 5345-7. PMID 20345186 DOI: 10.1021/Ja910666N |
0.742 |
|
| 2009 |
Chapdelaine D, Cardinal-David B, Prévost M, Gagnon M, Thumin I, Guindon Y. A stereoselective approach to nucleosides and 4'-thioanalogues from acyclic precursors. Journal of the American Chemical Society. 131: 17242-5. PMID 19902939 DOI: 10.1021/Ja905452F |
0.55 |
|
| 2009 |
Duplessis M, Waltz ME, Bencheqroun M, Cardinal-David B, Guindon Y. Stereoselective quaternary center construction via atom-transfer radical cyclization using silicon tethers on acyclic precursors. Organic Letters. 11: 3148-51. PMID 19552388 DOI: 10.1021/Ol901126Y |
0.649 |
|
| 2009 |
Duplessis M, Waltz M-, Bencheqroun M, Cardinal-David B, Guindon Y. Synthesis of Quaternary Stereocenters through a Radical Cyclization Synfacts. 2009: 990-990. DOI: 10.1055/S-0029-1217665 |
0.471 |
|
| 2006 |
Cardinal-David B, Brazeau JF, Katsoulis IA, Guindon Y. Phenylselenoethers as precursors of acyclic free radicals. Creating tertiary and quaternary centers using free radical-based intermediates Current Organic Chemistry. 10: 1939-1961. DOI: 10.2174/138527206778521259 |
0.515 |
|
| 2005 |
Cardinal-David B, Guérin B, Guindon Y. Synthesis of tertiary and quaternary stereogenic centers: a diastereoselective tandem reaction sequence combining Mukaiyama and free radical-based allylation. The Journal of Organic Chemistry. 70: 776-84. PMID 15675832 DOI: 10.1021/Jo048687J |
0.696 |
|
| 2002 |
Mochirian P, Cardinal-David B, Guérin B, Prévost M, Guindon Y. Synthesis of polypropionate motifs containing the anti-anti unit Tetrahedron Letters. 43: 7067-7071. DOI: 10.1016/S0040-4039(02)01557-5 |
0.64 |
|
| 2001 |
Guindon Y, Houde K, Prévost M, Cardinal-David B, Landry SR, Daoust B, Bencheqroun M, Guérin B. Synthesis of propionate motifs: diastereoselective tandem reactions involving anionic and free radical based processes. Journal of the American Chemical Society. 123: 8496-501. PMID 11525656 DOI: 10.1021/Ja010805M |
0.678 |
|
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