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 |
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Pages (from-to) | 2501-2503 |
Number of pages | 3 |
Journal | Bioscience, Biotechnology and Biochemistry |
Volume | 66 |
Issue number | 11 |
DOIs | |
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