[2,3]-Rearrangements of Ammonium Zwitterions

Hongli Bao, Uttam K. Tambar

Research output: Chapter in Book/Report/Conference proceedingChapter

10 Scopus citations

Abstract

The [2,3]-rearrangements of ammonium zwitterions are useful for the synthesis of nitrogen-containing chiral molecules. These rearrangements have served as key steps in the synthesis of complex natural products, which are discussed in this chapter. The [2,3]-rearrangement of amine N-oxides has become a powerful strategy for the total synthesis of natural products and other complex molecules. From a retrosynthetic perspective, there are several retrons associated with this process. For example, the identification of an O-allylhydroxylamine in the target molecule can guide the utilization of the Meisenheimer rearrangement in a total synthesis. The [2,3]-rearrangement of ammonium ylides has become a general strategy for the total synthesis of natural products and other target molecules. Retrosynthetically, α-allyl acid derivatives are common retrons for this sigmatropic process. Given the ubiquity of noncanonical amino acid substructures in naturally occurring small molecules, the Stevens rearrangement has emerged as a synthetically powerful transformation.

Original languageEnglish (US)
Title of host publicationMolecular Rearrangements in Organic Synthesis
Publisherwiley
Pages459-496
Number of pages38
ISBN (Electronic)9781118939901
ISBN (Print)9781118347966
DOIs
StatePublished - Oct 12 2015

Keywords

  • Amine N-oxides
  • Ammonium ylides
  • Ammonium zwitterions
  • Meisenheimer rearrangement
  • Stevens rearrangement
  • [2,3]-rearrangements

ASJC Scopus subject areas

  • Chemistry(all)

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