The asymmetric michael addition process involving chiral imines : stereochemical data in support of a cyclic-like transition state
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. Enantioselective synthesis of quaternary carbon centers through Michael-type alkylation of chiral imines
2. Enantioselective synthesis of ring-C aromatic steroids by asymmetric Michael-type alkylation of chiral imines.
3. Asymmetric intramolecular Michael reaction. Construction of chiral building blocks for the synthesis of several alkaloids
4. Toward a transition-state model in the asymmetric alkylation of chiral ketone secondary enamines by electron-deficient alkenes. A theoretical MO study
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2. Computational investigation of mechanistic aspects of the alkylation of chiral enamines;Journal of Molecular Structure: THEOCHEM;2007-07
3. Acyclic Stereocontrol in Michael Addition Reactions of Enamines and Enol Ethers;Topics in Stereochemistry;2007-02-26
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