Synthesis of model compounds of some biogenetic precursors of aflatoxin B1
- 1 January 1987
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1
- No. 1,p. 163-168
- https://doi.org/10.1039/p19870000163
Abstract
The synthesis of analogues of various natural products occurring during the biosynthesis of the notorious hepatocarcinogen aflatoxin B1(1) is described. These natural products are versiconol (21), versiconol acetate (22), versicolorin C (23), versiconal acetate (4), and 4-[2,3-dihydroxy-1-(hydroxymethyl)propyl]-3,8-dihydroxy-1-methoxyxanthone (24). The synthesis of an analogue of versiconal (5) is also described.This publication has 3 references indexed in Scilit:
- Polyketide-derived fungal metabolites from Bipolaris sorokiniana and their significance in the biosynthesis of sterigmatocystin and aflatoxin B1Journal of the Chemical Society, Perkin Transactions 1, 1984
- Structure and carbon-13 nuclear magnetic resonance assignments of versiconal acetate, versiconol acetate, and versiconol, metabolites from cultures of Aspergillus parasiticus treated with dichlorvosJournal of the Chemical Society, Perkin Transactions 1, 1979
- Biosynthesis of versiconal acetate, versiconol acetate, and versiconol, metabolites from cultures of Aspergillus parasiticus treated with dichlorvos. The role of versiconal acetate in aflatoxin biosynthesisJournal of the Chemical Society, Perkin Transactions 1, 1979