4.4 Article

Metal free organic transformation: cyanuric chloride catalyzed synthesis of 5-substituted-1H-tetrazoles

Journal

TETRAHEDRON LETTERS
Volume 56, Issue 17, Pages 2203-2206

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2015.03.032

Keywords

5-Substituted 1H-tetrazoles; Cyanuric chloride; [2+3] cycloaddition; Nitriles; Sodium azide

Funding

  1. Council of Scientific and Industrial Research, New Delhi, India [02(0025)/11/EMR-II]

Ask authors/readers for more resources

A wide variety of nitriles react with sodium azide in the presence of a catalytic amount of cyanuric chloride or 2,4,6-trichloro-1,3,5-triazine (TCT) under mild reaction conditions to give the corresponding 5-substituted-1H-tetrazoles in good to excellent yields. Here, we used TCT as a source of hydrochloric acid to catalyze this cycloaddition reaction. (C) 2015 Elsevier Ltd. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.4
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available