The cybrodins, a new class of sesquiterpenes
- 15 July 1981
- journal article
- research article
- Published by Canadian Science Publishing in Canadian Journal of Chemistry
- Vol. 59 (14) , 2150-2158
- https://doi.org/10.1139/v81-310
Abstract
The isolation and structure determination of the "cybrodins", a new group of sesquiterpenoids produced by a new strain of the bird's nest fungus Cyathus bulleri, is reported. Cybrodol (3), isocybrodol (4), cybrodal (5), trisnorcybrodolide (6), and cybrodic acid (7) may be classified as seco-illudalane sesquiterpenes. The evidence leading to the structural assignments is presented, along with chemical correlations among the cybrodins. The possible mode of biogenesis is discussed. Pterosin-C (13), a known norsesquiterpene, and 3-methyllumichrome (17) were also isolated. Small quantities of a new sesquiterpenoid, broderol, believed to possess structure 21, were obtained on two occasions.This publication has 4 references indexed in Scilit:
- The total synthesis of the cybrodinsCanadian Journal of Chemistry, 1981
- Chemical and toxicological studies on bracken fern, Pteridium aquilinum var. latiusculum. II. Structures of pterosins, sesquiterpenes having 1-indanone skeleton.CHEMICAL & PHARMACEUTICAL BULLETIN, 1978
- Metabolites of bird's nest fungi. Part 4. The isolation and structure determination of cybullol, a metabolite of Cyathus bulleri BrodieCanadian Journal of Chemistry, 1976
- Syntheses of isoalloxazines, alloxazines, toxoflavins, and fervenulins by oxidative cyclization of the Michael-type adducts from substituted 6-aminouracils and azo-compoundsJournal of the Chemical Society, Perkin Transactions 1, 1976