Cyanuric Chloride: an Efficient Catalyst for Ring Opening of Epoxides with Thiols Under Solvent-Free Conditions

Babasaheb P. Bandgar; Neeta S. Joshi; Vinod T. Kamble; Sanjay S. Sawant

doi:10.1071/CH07079

RESEARCH ARTICLE

Previous Contents Vol 61(3)

Cyanuric Chloride: an Efficient Catalyst for Ring Opening of Epoxides with Thiols Under Solvent-Free Conditions

Babasaheb P. Bandgar ^A ^B , Neeta S. Joshi ^A , Vinod T. Kamble ^A and Sanjay S. Sawant ^A

+ Author Affiliations

- Author Affiliations

^A Organic Chemistry Research Laboratory, School of Chemical Sciences, Swami Ramanand Teerth Marathwada University, Nanded 431606, Maharashtra, India.

^B Corresponding author. Email: bandgar_bp@yahoo.com

Australian Journal of Chemistry 61(3) 231-234 https://doi.org/10.1071/CH07079
Submitted: 15 March 2007 Accepted: 6 February 2008 Published: 26 March 2008

Abstract

2,4,6-Trichloro-1,3,5-triazine-catalyzed convenient and efficient ring opening of epoxides with thiols under solvent-free conditions is described. Short reaction time, mild reaction conditions, inexpensive and readily available catalyst, and excellent yields of products are attractive features of this methodology.

Acknowledgement

We thank Council of Scientific and Industrial Research, New Delhi, for financial assistance.

References

Cyanuric Chloride: an Efficient Catalyst for Ring Opening of Epoxides with Thiols Under Solvent-Free Conditions

Abstract

Acknowledgement

Subscriber Login