Asymmetric synthesis of R-β-amino butanoic acid and S-β-tyrosine: Homochiral lithium amide equivalents for Michael additions to α,β-unsaturated esters.-Reference-Cited by-同舟云学术

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

Published:1991-01 Issue:3 Volume:2 Page:183-186
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Davies Stephen G.,Ichihara Osamu

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference16 articles.

1. The ring opening of aziridine-2-carboxylate esters with organometallic reagents

2. General synthesis of enantiomerically pure β-amino acids

3. Stereoselective preparation of β-amino-acyl iron complexes for β-lactam synthesis

4. Transformations of chiral iron complexes used in organic synthesis. Reactions of .eta.5-CpFe(PPh3)(CO)COCH3 and related species leading to a mild, stereospecific synthesis of .beta.-lactams

5. Enantioselective synthesis of .beta.-amino esters through high pressure-induced addition of amines to .alpha.,.beta.-ethylenic esters

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