Sheldon A. Hiebert, Ph.D.
Affiliations: | 2003 | University of Toronto, Toronto, ON, Canada |
Area:
Organic SynthesisGoogle:
"Sheldon Hiebert"Mean distance: 8.38 | S | N | B | C | P |
Parents
Sign in to add mentor| Mark Lautens | grad student | 2003 | University of Toronto | |
| (Development of a palladium-catalyzed enantioselective ring -opening with dialkylzinc and its application to the total synthesis of ionomycin.) | ||||
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| Kodanko JJ, Hiebert S, Peterson EA, et al. (2007) Synthesis of all low-energy stereoisomers of the tris(pyrrolidinoindoline) alkaloid hodgkinsine and preliminary assessment of their antinociceptive activity. The Journal of Organic Chemistry. 72: 7909-14 |
| Becker MH, Chua P, Downham R, et al. (2007) Total synthesis of (-)-sarain A. Journal of the American Chemical Society. 129: 11987-2002 |
| Garg NK, Hiebert S, Overman LE. (2006) Total synthesis of (-)-sarain A. Angewandte Chemie (International Ed. in English). 45: 2912-5 |
| Douglas CJ, Hiebert S, Overman LE. (2005) Toward an enantioselective total synthesis of sarain A: construction of an advanced intermediate and rearrangement of the sarain A core under mild conditions. Organic Letters. 7: 933-6 |
| Lautens M, Hiebert S. (2004) Scope of palladium-catalyzed alkylative ring opening. Journal of the American Chemical Society. 126: 1437-47 |
| Lautens M, Colucci JT, Hiebert S, et al. (2002) Total synthesis of ionomycin using ring-opening strategies. Organic Letters. 4: 1879-82 |