Meha H. Shah, Ph.D.
Affiliations: | 2006 | Johns Hopkins University, Baltimore, MD |
Area:
mechanisms of redox reactions in proteinsGoogle:
"Meha Shah"Mean distance: 9.04 | S | N | B | C | P |
Parents
Sign in to add mentor| Justine P. Roth | grad student | 2006 | Johns Hopkins | |
| (Development and mechanistic studies of a bifunctional catalyst system: Lewis acid -Lewis base co-catalysis.) | ||||
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Publications
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| Bekele T, Shah MH, Wolfer J, et al. (2006) Catalytic, enantioselective [4 + 2]-cycloadditions of ketene enolates and o-quinones: efficient entry to chiral, alpha-oxygenated carboxylic acid derivatives. Journal of the American Chemical Society. 128: 1810-1 |
| France S, Shah MH, Weatherwax A, et al. (2005) Bifunctional Lewis acid-nucleophile-based asymmetric catalysis: mechanistic evidence for imine activation working in tandem with chiral enolate formation in the synthesis of beta-lactams. Journal of the American Chemical Society. 127: 1206-15 |
| France S, Wack H, Taggi AE, et al. (2004) Catalytic, asymmetric alpha-chlorination of acid halides. Journal of the American Chemical Society. 126: 4245-55 |
| Hafez AM, Dudding T, Wagerle TR, et al. (2003) A multistage, one-pot procedure mediated by a single catalyst: a new approach to the catalytic asymmetric synthesis of beta-amino acids. The Journal of Organic Chemistry. 68: 5819-25 |