Semipinacol rearrangement of cis-fused β-lactam diols into keto-bridged bicyclic lactams

Org Lett. 2012 May 4;14(9):2234-7. doi: 10.1021/ol300605y. Epub 2012 Apr 18.

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 N-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-exo trig carbamoyl radical cyclization, regioselective dithiocarbamate group elimination, and dihydroxylation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alcohols / chemical synthesis*
  • Alcohols / chemistry
  • Azabicyclo Compounds / chemical synthesis*
  • Azabicyclo Compounds / chemistry
  • Cyclization
  • Molecular Structure
  • Stereoisomerism
  • beta-Lactams / chemical synthesis*
  • beta-Lactams / chemistry

Substances

  • Alcohols
  • Azabicyclo Compounds
  • beta-Lactams