X = Y - ZH systems as potential 1,3-dipoles. Part 40. Chiral azomethine ylides from homochiral cyclic α-amino esters. Unusual regiospecific deprotonation of iminium ions.-Reference-Cited by-同舟云学术

X = Y - ZH systems as potential 1,3-dipoles. Part 40. Chiral azomethine ylides from homochiral cyclic α-amino esters. Unusual regiospecific deprotonation of iminium ions.

Published:1993-09 Issue:38 Volume:49 Page:8679-8690
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Grigg Ronald,Rankovic Zoran,Thornton-Pett Mark,Somasunderam Anoma

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference18 articles.

1. X=Y-ZH compounds as potential 1,3-Dipoles. Part 281,2 the iminium ion route to azomethine ylides. background and reaction of amines with bifunctional ketones.

2. X=Y-ZH compounds as potential 13-dipoles. Part 29. The iminium ion route to azomethine ylides. Reaction of cyclic secondary amines with mono- and bI- functional aldehydes

3. Allylic strain in six-membered rings

4. X = Y-ZH systems as potential 1,3-dipoles. part 27 Intramolecular cycloaddition reactions of imines of cyclic secondary α-amino esters. dipole and cycloaddition stereochemistry

5. X=Y-ZH Systems as potential 1,3-dipoles

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