Ruthenium-catalyzed one-pot carbenoid N-H insertion reactions and diastereoselective synthesis of prolines

Org Lett. 2008 Apr 17;10(8):1529-32. doi: 10.1021/ol800087p. Epub 2008 Mar 20.

Abstract

Aryl- and aliphatic-substituted 3-hydroxyprolines and various other amino esters are conveniently prepared by [RuCl2(p-cymene)]2-catalyzed one-pot intramolecular and intermolecular carbenoid N-H insertion reactions, respectively, and the prolines are formed with high diastereoselectivities. The catalytic reactions are tolerant toward air/moisture, and the product yields are insensitive to the organic solvents used.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Proline / chemical synthesis*
  • Ruthenium / chemistry*
  • Stereoisomerism

Substances

  • Ruthenium
  • Proline