Solid state conformations of α,β-unsaturated hydroxamates derived from the ‘chiral Weinreb amide’ auxiliary ( S )- N -1-(1′-naphthyl)ethyl- O - tert -butylhydroxylamine-Reference-Cited by-同舟云学术

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Solid state conformations of α,β-unsaturated hydroxamates derived from the ‘chiral Weinreb amide’ auxiliary ( S )- N -1-(1′-naphthyl)ethyl- O - tert -butylhydroxylamine

Published:2017-10 Issue:10 Volume:28 Page:1337-1341
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

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

Publisher

Elsevier BV

Subject

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

Reference18 articles.

1. The Chiral Auxiliary N-1-(1′-Naphthyl)ethyl-O-tert-butylhydroxylamine: A Chiral Weinreb Amide Equivalent

2. Alkylation and aldol reactions of acyl derivatives of N-1-(1′-naphthyl)ethyl-O-tert-butylhydroxylamine: asymmetric synthesis of α-alkoxy-, α-substituted-β-alkoxy- and α,β-dialkoxyaldehydes

3. Chiral relay auxiliaries

4. Chiral relay effects influence the facial selectivity of N-alkylated 5-phenylmorpholin-2-one enolates

5. On the origins of diastereoselectivity in the alkylation of diketopiperazine enolates

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