Biosynthesis of diterpenoid aphidicolin: Isolation of intermediates from P-450 inhibitor treated mycelia of Phoma betae
- 1 June 1999
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 55 (24) , 7541-7554
- https://doi.org/10.1016/s0040-4020(99)00392-0
Abstract
No abstract availableKeywords
This publication has 34 references indexed in Scilit:
- Useful approach to find the plausible biosynthetic precursors of secondary metabolites using P-450 inhibitors: postulated intermediates of chaetoglobosin AJournal of the Chemical Society, Perkin Transactions 1, 1992
- Structures of betaenones A and B, novel phytotoxins from Phoma betae Fr.Journal of the American Chemical Society, 1983
- A phytotoxin, betaenone C, and its related metabolites of Phoma betae Fr.Agricultural and Biological Chemistry, 1983
- Mode of Action of (E)-1-(2, 4-dichlorophenyl)-4, 4-dimethyl-2-(1, 2, 4-triazol-1-yl)-1-penten-3-ol (S-3308) in Ustilago maydisJournal of Pesticide Science, 1983
- Biogenetic-type total synthesis of (.+-.)-aphidicolinJournal of the American Chemical Society, 1983
- Efficient, stereoselective total synthesis of (.+-.)-aphidicolinJournal of the American Chemical Society, 1981
- Total synthesis of (.+-.)-aphidicolinJournal of the American Chemical Society, 1980
- A total synthesis of aphidicolinJournal of the American Chemical Society, 1979
- Isolation of aphidicolin as a root growth inhibitor from Harziella entomophilla.Agricultural and Biological Chemistry, 1978
- The production of aphidicolin by Nigrospora sphaericaCanadian Journal of Microbiology, 1974