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PubMed · 14787552

[Sulfone therapy].

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J COTTET. 1950-10-05. [Sulfone therapy].. https://pubmed.ncbi.nlm.nih.gov/14787552/

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N-sulfonylbenzotriazoles as advantageous reagents for C-sulfonylation.

[Structure: see text]. Reactions of readily available N-(alkyl-, aryl-, and heteroarylsulfonyl)benzotriazoles 3a-h with diverse nitriles, reactive heteroaromatics, alkylheteroaromatics, sulfones, and esters produced alpha-cyanoalkyl sulfones 5a-i, sulfonylheteroaromatics 7a-e, alpha-(sulfonylalkyl)heterocycles 9a-f, alpha-sulfonylalkyl sulfones 11a-g, and esters of alpha-sulfonyl acids 14a-c, respectively, in synthetically useful to excellent yields. The results represent the first examples of the successful application of sulfonylazoles for C-sulfonylation.

Sulfones↗