Diastereoselective iodocarbocyclization reaction of 8-phenylmenthyl allylmalonate: An efficient preparation of a synthetic intermediate of cyclopropane amino acids

Tadashi Inoue, Osamu Kitagawa, Orie Ochiai, Takeo Taguchi

Research output: Contribution to journalArticle

25 Citations (Scopus)

Abstract

The iodocarbocyclization of allylmalonate using (-)-8-phenylmenthol as a chiral auxiliary proceeded with high diastereoselectivity to give the iodomethylcyclopropane dicarboxylic ester in good yield.

Original languageEnglish
Pages (from-to)691-692
Number of pages2
JournalTetrahedron: Asymmetry
Volume6
Issue number3
DOIs
Publication statusPublished - 1995
Externally publishedYes

    Fingerprint

ASJC Scopus subject areas

  • Catalysis
  • Inorganic Chemistry
  • Organic Chemistry
  • Physical and Theoretical Chemistry
  • Materials Chemistry
  • Drug Discovery

Cite this