Enantio- and diastereoselective synthesis of γ-amino alcohols

Chem Commun (Camb). 2015 Oct 4;51(77):14462-4. doi: 10.1039/c5cc04445f. Epub 2015 Aug 14.

Abstract

The γ-amino alcohol structural motif is often encountered in drugs and natural products. We developed two complementary catalytic diastereoselective methods for the synthesis of N-PMP-protected γ-amino alcohols from the corresponding ketones. The anti-products were obtained through Ir-catalyzed asymmetric transfer hydrogenation, the syn-products via Rh-catalyzed asymmetric hydrogenation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Alcohols / chemical synthesis*
  • Amino Alcohols / chemistry
  • Catalysis
  • Hydrogenation
  • Stereoisomerism

Substances

  • Amino Alcohols