Synthesis of fused 1,2,4-thiadiazolines by intramolecular cycloaddition-elimination reactions of 4-methyl-5-(cyano tethered)imino-Δ2-1,2,3,4-thiatriazolines-Reference-Cited by-同舟云学术

Synthesis of fused 1,2,4-thiadiazolines by intramolecular cycloaddition-elimination reactions of 4-methyl-5-(cyano tethered)imino-Δ2-1,2,3,4-thiatriazolines

Published:1992-09 Issue:36 Volume:48 Page:7505-7518
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

L'abbé Gerrit,Leurs Stefan

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference21 articles.

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

2. 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

3. Influence of Pyridine on the Ring Transformations of 4-Alkyl-5-Arylimino-Δ2-1,2,3,4-Thiatriazolines With Aryl Isothiocyanates

4. Mechanism of the cycloaddition-elimination reactions of 4-methyl-5-phenylimino-δ2-1,2,3,4-thiatriazoline with alkyl and aryl isothiocyanates

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

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