Skip to main navigation Skip to search Skip to main content

The Vinylogous Mukaiyama Aldol Reaction in Natural Product Synthesis

Research output: Chapter in book/report/conference proceedingContribution to book/anthologyResearchpeer review

Abstract

The aldol reaction is one of the most predominantly used reactions for the formation of C-C bonds in synthetic organic chemistry. The vinylogous extension of this fundamental C-C bond-forming reaction, the VMAR, is unique in its atomic economy in the generation of hydroxycarbonyl compounds. The generation of the same hydroxycarbonyl compounds via other routes is sometimes cumbersome and often requires multi-step synthetic sequences. Therefore, the VMAR can be a powerful alternative to other strategies in the rational design of polyketide fragments of complex natural products. In this chapter, recent advances in the VMAR and its applications to natural product synthesis are discussed.

Original languageEnglish
Title of host publicationModern Methods in Stereoselective Aldol Reactions
PublisherWiley-VCH Verlag
Pages83-154
Number of pages72
ISBN (Print)9783527332052
DOIs
Publication statusPublished - 6 Feb 2013

Keywords

  • Asymmetric
  • Butenolides
  • D4 donors
  • Diastereoselective
  • Enantioselective
  • Natural product synthesis
  • Polyketides
  • Vinylogous Mukaiyama aldol reaction
  • Vinylogy

ASJC Scopus subject areas

  • General Chemistry

Cite this