Approaches to Asymmetric Synthesis. The Diastereoselective Alkylations of Chiral Propionamide Enolates

Approaches to Asymmetric Synthesis. The Diastereoselective Alkylations of Chiral Propionamide Enolates

<p>Enantioselective propionate alkylation, as a method to control acyclic methyl~bearing stereocenters, is achieved via the diastereoselective alkylation of chiral propionamide enolates. The factors which control stereoselective enolization, diastereotopic differentiation of the enolate system...

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Bibliographic Details
Main Author: Takacs, James Michael
Format: Others
Language:en
Published: 1981
Online Access:https://thesis.library.caltech.edu/10869/1/Takacs_JM_1981.pdf
Takacs, James Michael (1981) Approaches to Asymmetric Synthesis. The Diastereoselective Alkylations of Chiral Propionamide Enolates. Dissertation (Ph.D.), California Institute of Technology. doi:10.7907/f2kf-9406. https://resolver.caltech.edu/CaltechTHESIS:05092018-115015856 <https://resolver.caltech.edu/CaltechTHESIS:05092018-115015856>

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https://thesis.library.caltech.edu/10869/1/Takacs_JM_1981.pdf
Takacs, James Michael (1981) Approaches to Asymmetric Synthesis. The Diastereoselective Alkylations of Chiral Propionamide Enolates. Dissertation (Ph.D.), California Institute of Technology. doi:10.7907/f2kf-9406. https://resolver.caltech.edu/CaltechTHESIS:05092018-115015856 <https://resolver.caltech.edu/CaltechTHESIS:05092018-115015856>

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