X=Y-ZH compounds as potential 1,3-Dipoles. Part 231,2 mechanisms of the reactions of ninhydrin and phenalene trion with ∝-amino acids. X-ray crystal structure of protonated ruhemann's purple, a stable azomethine ylide-Reference-Cited by-同舟云学术

X=Y-ZH compounds as potential 1,3-Dipoles. Part 231,2 mechanisms of the reactions of ninhydrin and phenalene trion with ∝-amino acids. X-ray crystal structure of protonated ruhemann's purple, a stable azomethine ylide

Published:1989-01 Issue:12 Volume:45 Page:3849-3862
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Grigg Ronald,F. Malone John,Mongkolaussavaratana Theeravat,Thianpatanagul Sunit

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference60 articles.

1. X=y-zh systems as potential 1,3-dipoles

2. Cycloaddition reaction relevant to the mechanism of the ninhydrin reaction. X-Ray crystal structure of protonated Ruhemann's purple, a stable 1,3-dipole

3. CXXXII.—Cyclic di- and tri-ketones

4. CCXII.—Triketohydrindene hydrate

5. LXXXIV.—Triketohydrindene hydrate. Part III. Its relation to alloxan

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