Semipinacol Rearrangement of <i>Cis</i>-Fused β-Lactam Diols into Keto-Bridged Bicyclic Lactams

Abstract

The 6-azabicyclo[3.2.1]octane ring system, prevalent in a range of biologically active molecules, is prepared through a novel semipinacol rearrangement utilizing a cyclic phosphorane or sulfite intermediate. The rearrangement proceeds with exclusive <i>N</i>-acyl group migration of a β-lactam ring and results in carbonyl functionality at the 7- and bridging 8-position of the bicycle. Precursor ring-fused β-lactam diols are prepared through a sequence of 4-<i>exo trig</i> carbamoyl radical cyclization, regioselective dithiocarbamate group elimination, and dihydroxylation