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.-Reference-Cited by-同舟云学术

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.

Published:1990-01 Issue:18 Volume:46 Page:6433-6448
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Ardill Harriet,Dorrity M.J.R.,Grigg Ronald,Leon-Ling Mooi-Sin,Malone J.F.,Sridharan Visuvanathar,Thianpatanagul. Sunit

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference32 articles.

1. 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

2. Iminium ion route to azomethine yields from primary and secondary amines

3. Prototropic routes to 1,3- and 1,5-dipoles, and 1,2-ylides: applications to the synthesis of heterocyclic compounds

4. XY–ZH systems as potential 1,3-dipoles. Part 3. Isoxazolidines from the 1:1 cycloaddition of oximes with dipolarophiles

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

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