Acylation of Ambident Vinylogous Urethanes Exocyclic to Thiazolidines and Reduced Thiazines-Reference-Cited by-同舟云学术

Acylation of Ambident Vinylogous Urethanes Exocyclic to Thiazolidines and Reduced Thiazines

Published:2006-09 Issue:9 Volume:2006 Page:580-583
ISSN:1747-5198
Container-title:Journal of Chemical Research
language:en
Short-container-title:Journal of Chemical Research

Author:

Avent Anthony G.¹,Loakes David¹,Young Douglas W.¹

Affiliation:

1. Department of Chemistry, University of Sussex, Falmer, Brighton BN1 9QJ, UK

Abstract

The vinylogous thiazine urethanes 1 are invariably acylated on carbon and not on nitrogen, even when the carbon is “blocked” as in 18. The analogous thiazolidine 2 is acylated either on carbon or nitrogen, depending on the electrophile used.

Publisher

SAGE Publications

Subject

General Chemistry

Link

http://journals.sagepub.com/doi/pdf/10.3184/030823406778521365

Reference6 articles.

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5. 221. Studies related to cephalosporin C. Part III. A synthetical route to 6H-1,3-thiazines and the synthesis of a new fragmentation product of a cephalosporanic acid derivative

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2. Acetic Formic Anhydride;Encyclopedia of Reagents for Organic Synthesis;2008-09-15

3. Acylation of Ambident Vinylogous Urethanes Exocyclic to Thiazolidines and Reduced Thiazines.;ChemInform;2007-01-16