Acyclic stereocontrol through the dianionic Claisen rearrangement of .beta.-hydroxy esters: synthesis of (.+-.)-botryodiplodin
- 1 May 1985
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 50 (11) , 1840-1845
- https://doi.org/10.1021/jo00211a010
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
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- Diastereoselective benzyloxymercuration/demercuration of derivatives of .gamma.-alkyl-.delta.-hydroxy-.alpha.,.beta.-unsaturated esters. A new strategy for the synthesis of aldol-type productsJournal of the American Chemical Society, 1983
- Botryodiplodin, a mycotoxin synthesized by a strain of P. roquefortiThe Journal of Organic Chemistry, 1982
- Mutagenicity of the mycotoxin botryodiplodin in the salmonella typhimurium/microsomal activation testEnvironmental Mutagenesis, 1981