Chemoselective ligation of sulfinic acids with aryl-nitroso compounds.

Angew Chem Int Ed Engl

Department of Chemistry, The Scripps Research Institute, 130 Scripps Way, Jupiter, FL 33458, USA.

Published: June 2012

Making a comeback: The inefficient condensation of sulfinic acid and aryl nitroso compounds has been transformed into a chemoselective process that converts sulfinic acid into stable cyclic sulfonamide analogues (see scheme). This ligation proceeds rapidly under aqueous conditions in high yield, and lays the groundwork for the development of sulfinic acid detection methods in biological systems.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3523331PMC
http://dx.doi.org/10.1002/anie.201201812DOI Listing

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