Excellent diastereoselective allylation of camphor derived glyoxylic oxime ethers mediated by a Lewis acid

Neelesh A. Kulkarni, Kwunmin Chen

Research output: Contribution to journalArticle

16 Citations (Scopus)

Abstract

The nucleophilic allylation of camphor derived glyoxylic oxime ethers was carried out using allyltributyltin in the presence of Sn(OTf)2 affording the corresponding homoallylic amines in high chemical yields (up to 94%) and excellent stereoselectivities (up to >99%).

Original languageEnglish
Pages (from-to)611-613
Number of pages3
JournalTetrahedron Letters
Volume47
Issue number4
DOIs
Publication statusPublished - 2006 Jan 23

    Fingerprint

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

Cite this