Synthesis of both enantiomers of isorobinal, a novel cyclic monoterpene isolated from the astigmatid mite, rhizoglyphus sp.

Ting Liang, Shigefumi Kuwahara

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

Both enantiomers of isorobinal, a cyclic monoterpene isolated from the astigmatid mite (Rhizoglyphus sp.), were synthesized from the enantiomers of perillaldehyde in four steps by using PCC-oxidation of a tertiary allylic alcohol intermediate as the key step.

Original languageEnglish
Pages (from-to)2501-2503
Number of pages3
JournalBioscience, Biotechnology and Biochemistry
Volume66
Issue number11
DOIs
Publication statusPublished - 2002 Jan 1

Keywords

  • Isorobinal
  • Rhizoglyphus
  • Terpenoid

ASJC Scopus subject areas

  • Biotechnology
  • Analytical Chemistry
  • Biochemistry
  • Applied Microbiology and Biotechnology
  • Molecular Biology
  • Organic Chemistry

Fingerprint Dive into the research topics of 'Synthesis of both enantiomers of isorobinal, a novel cyclic monoterpene isolated from the astigmatid mite, rhizoglyphus sp.'. Together they form a unique fingerprint.

  • Cite this