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

24 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

cyclopropane
amino acids
Amino acids
esters
Esters
Amino Acids
preparation
8-phenylmenthol

ASJC Scopus subject areas

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

Cite this

Diastereoselective iodocarbocyclization reaction of 8-phenylmenthyl allylmalonate : An efficient preparation of a synthetic intermediate of cyclopropane amino acids. / Inoue, Tadashi; Kitagawa, Osamu; Ochiai, Orie; Taguchi, Takeo.

In: Tetrahedron: Asymmetry, Vol. 6, No. 3, 1995, p. 691-692.

Research output: Contribution to journalArticle

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