Stereocontrolled dihydroxylation reactions of acyclic allylic amines

Jongho Jeon, Nara Shin, Young Gyu Kim

Research output: Contribution to journalReview articlepeer-review

3 Scopus citations

Abstract

The dihydroxylation reaction of allylic amines is a facile and useful synthetic method to obtain amino diol structures that are widely found in lots of biologically important natural products. This review will focus on the recent methods of both substrate-controlled and ligand-controlled dihydroxylation reactions of acyclic allylic amines. In addition, several applications of the diastereoselective dihydroxylation methods to asymmetric syntheses of natural products are presented.

Original languageEnglish
Pages (from-to)437-446
Number of pages10
JournalApplied Chemistry for Engineering
Volume25
Issue number5
DOIs
StatePublished - 1 Oct 2014

Keywords

  • Acyclic conformation
  • Asymmetric synthesis
  • Dihydroxylation
  • Natural product
  • Osmium tetroxide

Fingerprint

Dive into the research topics of 'Stereocontrolled dihydroxylation reactions of acyclic allylic amines'. Together they form a unique fingerprint.

Cite this