3-Aryl-1-benzoylthioureas with α-bromoketones in Water form 2-N-benzoyl-3-arylthiazol-2(3H)-imines, not 3-aryl-1-benzoylimidazoline-2-thiones-Reference-Cited by-同舟云学术

3-Aryl-1-benzoylthioureas with α-bromoketones in Water form 2-N-benzoyl-3-arylthiazol-2(3H)-imines, not 3-aryl-1-benzoylimidazoline-2-thiones

Published:2007-03 Issue:3 Volume:2007 Page:136-137
ISSN:1747-5198
Container-title:Journal of Chemical Research
language:en
Short-container-title:Journal of Chemical Research

Author:

Singh C.B.¹,Murru Siva¹,Kavala Veerababurao¹,Patel Bhisma K.¹

Affiliation:

1. Department of Chemistry, Indian Institute of Technology Guwahati, Guwahati 781 039, Assam, India

Abstract

The products obtained by the reaction of 1-benzoyl-3-phenylthioureas with α-bromoketones in water in the presence of triethylamine are not imidazoline-2-thiones as reported (J. Chem. Res. 2005, 689–690); rather they are thiazol-2-imine derivatives.

Publisher

SAGE Publications

Subject

General Chemistry

Link

http://journals.sagepub.com/doi/pdf/10.3184/030823407X196719

Reference5 articles.

1. It Is “Thiazolidene-2-imine” and Not Imidazole-2-thione as the Reaction Product of 1-Benzoyl-3-phenylthiourea with Br2/Enolizable Ketone

2. Novel Synthesis of 1-Aroyl-3-aryl-4-substituted Imidazole-2-thiones

3. An efficient and clean synthesis of 1-aroyl-3-aryl-4-substituted imidazole-2-thiones in water

4. Stereoselective Organic Reactions in Water

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