X=Y–ZH systems as potential 1,3-dipoles. Part 57: Cascade 1,3-azaprotio cyclotransfer–cycloaddition reactions between aldoximes and divinyl ketone: remarkable rate enhancement and control of cycloaddition regiochemistry by Lewis acids-Reference-Cited by-同舟云学术

X=Y–ZH systems as potential 1,3-dipoles. Part 57: Cascade 1,3-azaprotio cyclotransfer–cycloaddition reactions between aldoximes and divinyl ketone: remarkable rate enhancement and control of cycloaddition regiochemistry by Lewis acids

Published:2002-09 Issue:38 Volume:58 Page:7727-7733
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Dunn Peter J,Graham Alison B,Grigg Ronald,Higginson Paul,Thornton-Pett Mark

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference11 articles.

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

2. Blackwell, M.; Dunn, P. J.; Graham, A. B.; Grigg, R.; Higginson, P.; Saba, I. S.; Thornton-Pett, M.; Tetrahedron, 2002, 58, 7715–7725.

3. Catalytic enantioselective 1,3-dipolar cycloaddition reactions of nitrones

4. A new synthetic access to N-alkylated nitrones through Lewis acid-catalyzed conjugate additions of aldoximes

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