Adaptation of a small-molecule hydrogen-bond donor catalyst to an enantioselective hetero-Diels-Alder reaction hypothesized for brevianamide biosynthesis

Org Lett. 2015 Feb 20;17(4):880-3. doi: 10.1021/ol503626w. Epub 2015 Jan 31.

Abstract

Chiral diamine-derived hydrogen-bond donors were evaluated for their ability to effect stereocontrol in an intramolecular hetero-Diels-Alder (HDA) reaction hypothesized in the biosynthesis of brevianamides A and B. Collectively, these results provide proof of principle that small-molecule hydrogen-bond catalysis, if even based on a hypothetical biosynthesis construct, holds significant potential within enantioselective natural product synthesis.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkaloids / chemical synthesis*
  • Alkaloids / chemistry
  • Cycloaddition Reaction
  • Hydrogen Bonding
  • Molecular Structure
  • Piperazines / chemical synthesis*
  • Piperazines / chemistry
  • Spiro Compounds / chemical synthesis
  • Spiro Compounds / chemistry
  • Stereoisomerism

Substances

  • Alkaloids
  • Piperazines
  • Spiro Compounds
  • brevianamide A
  • brevianamide B