Superoxide‐Mediated Regioselective Deblocking of the Tosyl Group from N‐Tosylcarboxamides

R. S. Raghuvanshi Department of Applied Chemistry, Institute of Technology, Banaras Hindu University, Varanasi, India

K. N. Singh Department of Applied Chemistry, Institute of Technology, Banaras Hindu University, Varanasi, IndiaCorrespondence[email protected]

Abstract

In situ–generated tetraethylammonium superoxide brings about an easy and selective cleavage of the N[sbnd]S bond of N‐tosylcarboxamides, providing a new method for the deblocking of the tosyl group from such substrates.

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Acknowledgment

The authors thank Council of Scientific and Industrial Research (CSIR), New Delhi, for financial support.

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Superoxide‐Mediated Regioselective Deblocking of the Tosyl Group from N‐Tosylcarboxamides

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Superoxide‐Mediated Regioselective Deblocking of the Tosyl Group from N‐Tosylcarboxamides

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