Double asymmetric induction as a mechanistic probe: the doubly diastereoselective conjugate addition of enantiopure lithium amides to enantiopure α,β-unsaturated esters and enantiopure α,β-unsaturated hydroxamates-Reference-Cited by-同舟云学术

Double asymmetric induction as a mechanistic probe: the doubly diastereoselective conjugate addition of enantiopure lithium amides to enantiopure α,β-unsaturated esters and enantiopure α,β-unsaturated hydroxamates

Published:2011-08 Issue:34 Volume:67 Page:6382-6403
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Davies Stephen G.,Lee James A.,Roberts Paul M.,Thomson James E.,Yin Jingda

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference106 articles.

1. Asymmetric synthesis of R-β-amino butanoic acid and S-β-tyrosine: Homochiral lithium amide equivalents for Michael additions to α,β-unsaturated esters.

2. Origins of the high stereoselectivity in the conjugate addition of lithium(α-methylbenzyl)benzylamide to t-butyl cinnamate

3. Homochiral lithium amides for the asymmetric synthesis of β-amino acids

4. Iodine-mediated ring-closing iodoamination with concomitant N-debenzylation for the asymmetric synthesis of polyhydroxylated pyrrolidines

5. Doubly diastereoselective [3,3]-sigmatropic aza-Claisen rearrangements

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