Ring-closure reactions of functionalized vinyl sulfonamides

Chem. Heterocycl. Compd. 2021, 57 (6), 630-632

DOI: 10.1007/s10593-021-02960-0

Dodrydnev A.; Omelian T.

Diversity-oriented synthesis embodied in a strategy of pairing vinyl sulfonamide moiety with other functional groups resulted in an array of skeletally diverse 5–8-membered sultams (cyclic sulfonamides) in the fewest possible steps. In particular, this strategy allows utilization of a number of cyclization protocols including intramolecular Michael, Diels–Alder, Heck, Pauson–Khand, Baylis–Hillman reactions, ring-closing metathesis (RCM) and others.

Ring-closure reactions of functionalized vinyl sulfonamides

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