Regiospecific Cleavage of S–N Bonds in Sulfonyl Azides: Sulfonyl Donors
Zhiguo Zhang, Songnan Wang, Yong Zhang, Guisheng Zhang
Abstract
Zhiguo Zhang, Songnan Wang, Yong Zhang, Guisheng Zhang
Abstract
Sulfonyl azides have been widely used as sulfonamido, diazo, and azido donors, as well as all-nitrogen 1,3-dipoles donors in synthetic chemistry. Here, the sulfonyl azides were used as efficient sulfonyl donors, which is very unusual. Trifluoromethanesulfonic acid-induced formation of the sulfonyl cation reactive species from sulfonyl azides was developed and used for the first time to couple various inactivated arenes to prepare sulfones at ambient temperature.
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Sulfonyl azides have been widely used as sulfonamido, diazo, and azido donors, as well as all-nitrogen 1,3-dipoles donors in synthetic chemistry. Here, the sulfonyl azides were used as efficient sulfonyl donors, which is very unusual. Trifluoromethanesulfonic acid-induced formation of the sulfonyl cation reactive species from sulfonyl azides was developed and used for the first time to couple various inactivated arenes to prepare sulfones at ambient temperature.
Key concepts: Sulfonyl, Chemistry, Diazo, Cleavage (geology), Organic chemistry, Medicinal chemistry, Geotechnical engineering, Alkyl