Secondary mould metabolites. Part 29. Isolation and structure elucidation of candicansol, 3-epi-illudol and 1-O-acetyl-3-epi-illudol, novel sesquiterpenoids from Clitocybe candicans, and absolute configuration of 3-epi-illudol
- 1 January 1989
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1
- No. 11,p. 1995-2000
- https://doi.org/10.1039/p19890001995
Abstract
The structural elucidation of candicansol (1a), 3-epi-illudol (2a), and 1-O-acetyl-3-epi-illudol (3), novel illudalane and protoilludane sesquiterpenoids isolated from cultures of Clitocybe candicans is based on a study of their 1H and 13C n.m.r. spectral data. The absolute configuration of 3-epi-illudol is also reported.This publication has 4 references indexed in Scilit:
- Secondary mould metabolites. Part 19. Structure elucidation and absolute configuration of melledonals B and C, novel antibacterial sesquiterpenoids from Armillaria mellea. X-Ray molecular structure of melledonal CJournal of the Chemical Society, Perkin Transactions 1, 1988
- Sulcatine, a norsesquiterpene from the fungus Laurilia sulcataPhytochemistry, 1987
- Structures of melleolides B-D, three antibacterial sesquiterpenoids from Armillaria melleaPhytochemistry, 1986
- Synthesis of racemic fomannosin and illudol using a biosynthetically patterned common intermediateJournal of the American Chemical Society, 1982