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

Ting Liang; Shigefumi Kuwahara

doi:10.1271/bbb.66.2501

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 journal › Article › peer-review

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 language	English
Pages (from-to)	2501-2503
Number of pages	3
Journal	Bioscience, Biotechnology and Biochemistry
Volume	66
Issue number	11
DOIs	https://doi.org/10.1271/bbb.66.2501
Publication status	Published - 2002 Jan 1

Keywords

Isorobinal
Rhizoglyphus
Terpenoid

ASJC Scopus subject areas

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

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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.",

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KW - Terpenoid

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

Abstract

Keywords

ASJC Scopus subject areas

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