X=Y–ZH systems as potential 1,3-dipoles. Part 56: Cascade 1,3-azaprotio cyclotransfer–cycloaddition reactions between aldoximes and divinyl ketone: the effect of oxime E/Z isomerism on cycloaddition stereoselectivity-Reference-Cited by-同舟云学术

X=Y–ZH systems as potential 1,3-dipoles. Part 56: Cascade 1,3-azaprotio cyclotransfer–cycloaddition reactions between aldoximes and divinyl ketone: the effect of oxime E/Z isomerism on cycloaddition stereoselectivity

Published:2002-09 Issue:38 Volume:58 Page:7715-7725
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Blackwell Mark,Dunn Peter J,Graham Alison B,Grigg Ronald,Higginson Paul,Saba Imaad S,Thornton-Pett Mark

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference25 articles.

1. Part 55. Dunn, P. J.; Graham, A. B.; Grigg, R.; Saba, I. S.; Thornton-Pett, M. Tetrahedron, 2002, 58, 7701–7713.

2. X=Y-ZH systems as potential 1,3-dipoles. Part 31. Generation of nitrones from oximes. Background and scope of the tandem 1,2-prototropy-intramolecular cycloaddition sequence.

3. X=Y-ZH systems as potential 1,3-dipoles. Part 32 generation of nitrones from oximes. Tandem Michael addition-1,3-dipolar cycloaddition reactions. Background and class 1 processes.

4. X=Y-ZH systems as potential 1,3-dipoles. Part 33. Generation of nitrones from oximes. Tandem Michael addition-1,3-dipolar cycloaddition reactions. Class 2 processes in which the dipolarophile is located within the oxime.

5. X=Y-ZH systems as potential 1,3-dipoles. Part 34. generation of nitrones from oximes. Tandem michael addition-1,3-dipolar cycloaddition reactions. class 2 processes utilising bifunctional michael acceptor-dipolarophile components.

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