Abstract
The naturally occurring (-)-enantiomer of a fatty acid isolated from the mushroom (Hericium erinaceum) was synthesized from (R)-(-)-benzyl glycidyl ether in 8 steps. A comparison of the specific rotation of the synthetic sample with that of the natural Compound established the absolute configuration of the latter.
Original language | English |
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Pages (from-to) | 1417-1419 |
Number of pages | 3 |
Journal | Bioscience, Biotechnology and Biochemistry |
Volume | 56 |
Issue number | 9 |
DOIs | |
Publication status | Published - 1992 |
Externally published | Yes |
ASJC Scopus subject areas
- Biotechnology
- Analytical Chemistry
- Biochemistry
- Applied Microbiology and Biotechnology
- Molecular Biology
- Organic Chemistry