Strain-driven direct cross-aldol and -ketol reactions of four-membered heterocyclic ketones

Org Lett. 2015 Jun 5;17(11):2634-7. doi: 10.1021/acs.orglett.5b01002. Epub 2015 May 11.

Abstract

Owing to the ring strain and α-heteroatom effect, the four-membered heterocyclic ketones can undergo direct cross-aldol and -ketol reactions without the need for preformed enol or "enolate-like" intermediates. Besides the organocatalyzed cross-ketol addition onto their highly active carbonyl group, their ability to act as a nucleophilic donor has also been explored. As a result, a number of discrete aldol adducts were synthesized and the distinct reactivities were successfully combined into a double-aldol one-pot reaction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alcohols / chemical synthesis*
  • Alcohols / chemistry
  • Aldehydes / chemical synthesis*
  • Aldehydes / chemistry
  • Heterocyclic Compounds / chemistry*
  • Ketones / chemical synthesis*
  • Ketones / chemistry*
  • Molecular Structure

Substances

  • Alcohols
  • Aldehydes
  • Heterocyclic Compounds
  • Ketones