Cycloaddition-elimination reactions of 4-methyl-5-phenylimino Δ2-1,2,3,4-thiatriazoline with strong electrophilic isothiocyanates. Mechanism of the isomerization process-Reference-Cited by-同舟云学术

Cycloaddition-elimination reactions of 4-methyl-5-phenylimino Δ2-1,2,3,4-thiatriazoline with strong electrophilic isothiocyanates. Mechanism of the isomerization process

Published:1990-01 Issue:4 Volume:46 Page:1281-1286
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

L'abbé Gerrit,Buelens Karin

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference11 articles.

1. 4-Alkyl-5-(arylimino)-1,2,3,4-thiatriazolines as masked 1,3-dipoles

2. Some ring-transformation reactions of sulfur-containing heterocycles

3. A rare case of three rearrangements during the cycloaddition-elimination reaction of 4-methyl-5-phenylimino-Δ2-1,2,3,4-thiatriazoline with 2-pyridyl isothiocyanate

4. The Chemistry of Hypervalent Molecules

5. "Frozen" Transition States: Pentavalent Carbon et al.

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1. On the Cycloaddition-Elimination Reactions of 1,2,3,4-Thiatriazoline-5-Imines with Ketenes;Bulletin des Sociétés Chimiques Belges;2010-09-01

2. Isomerizations of 1,2,4-Thiadiazolidines via Thiapentalene Intermediates;Bulletin des Sociétés Chimiques Belges;2010-09-01

3. On the Mechanism of the Reactions of 4-Alkyl-5-Arylimino-1,2,3,4-Thiatriazolines with Isocyanates;Bulletin des Sociétés Chimiques Belges;2010-09-01

4. Cycloaddition−Elimination Reactions of 5-Imino-1,2,4-thiadiazolidin-3-ones and 5-Imino-1,2,4-dithiazolidin-3-ones with Electron-Rich Double Bonds;European Journal of Organic Chemistry;1998-03

5. Volume 4 References;Comprehensive Heterocyclic Chemistry II;1996