Doubly diastereoselective conjugate additions of the antipodes of lithium N-benzyl-N-(α-methylbenzyl)amide to enantiopure ε-O-protected α,β-unsaturated esters derived from d-ribose-Reference-Cited by-同舟云学术

Doubly diastereoselective conjugate additions of the antipodes of lithium N-benzyl-N-(α-methylbenzyl)amide to enantiopure ε-O-protected α,β-unsaturated esters derived from d-ribose

Published:2014-04 Issue:6-7 Volume:25 Page:534-546
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Davies Stephen G.,Foster Emma M.,Lee James A.,Roberts Paul M.,Thomson James E.

Publisher

Elsevier BV

Subject

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

Reference38 articles.

1. Double Asymmetric Synthesis and a New Strategy for Stereochemical Control in Organic Synthesis

2. An Oxidation and Ring Contraction Approach to the Synthesis of (±)-1-Deoxynojirimycin and (±)-1-Deoxyaltronojirimycin

3. Syntheses of the Enantiomers of 1-Deoxynojirimycin and 1-Deoxyaltronojirimycin via Chemo- and Diastereoselective Olefinic Oxidation of Unsaturated Amines

4. Concise and highly selective asymmetric synthesis of acosamine from sorbic acid

5. Highly Diastereoselective and Stereodivergent Dihydroxylations of Acyclic Allylic Amines: Application to the Asymmetric Synthesis of 3,6-Dideoxy-3-amino-l-talose

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