Diastereoselective reduction of ketimines derived from (R)-3,4-dihydroxybutan-2-one: an alternative route to key intermediates for the synthesis of anticancer agent ES-285-Reference-Cited by-同舟云学术

Diastereoselective reduction of ketimines derived from (R)-3,4-dihydroxybutan-2-one: an alternative route to key intermediates for the synthesis of anticancer agent ES-285

Published:2010-03 Issue:4 Volume:21 Page:503-506
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Allepuz Ana C.,Badorrey Ramón,Díaz-de-Villegas María D.,Gálvez José A.

Publisher

Elsevier BV

Subject

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

Reference29 articles.

1. Study of the Reactions between Vinylmagnesium Bromide and Imines Derived from (R)-Glyceraldehyde − The Key Step in the Stereodivergent Synthesis of Conveniently Protected, Enantiopure syn- and anti-2-Amino-1,3,4-butanetriol Derivatives

2. Efficient stereodivergent synthesis of 1,4-dideoxy-1,4-iminohexitols from an (S)-glyceraldimine

3. Asymmetric Homologation of Ketones. A New Entry to Orthogonally Protected (2R,4R)-Piperidine-2,4-dicarboxylic Acid

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