1,5-Rhodium Shift in Rearrangement of <i>N</i>‑Arenesulfonylazetidin-3-ols into Benzosultams
收藏NIAID Data Ecosystem2026-03-08 收录
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Benzosultams are synthesized in an enantiopure form starting from α-amino acids through a rhodium-catalyzed rearrangement reaction of N-arenesulfonylazetidin-3-ols. Mechanistically, this reaction involves C–C bond cleavage by β-carbon elimination and C–H bond cleavage by a 1,5-rhodium shift.
创建时间:
2016-02-18



