Absolute configuration of A-32'287 [conocandin] and total synthesis of its methyl and tert-butyl esters
- 1 November 1987
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 52 (24) , 5452-5457
- https://doi.org/10.1021/jo00233a028
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
- High diastereoface selection in an ester enolate addition to .alpha.-alkoxy aldehydes: stereoselective synthesis of .alpha.-methylene-.beta.-hydroxy-.gamma.-alkoxy estersThe Journal of Organic Chemistry, 1984
- Highly stereoselective synthesis of trisubstituted olefins via addition of alkylcopper complexes to acetylenesThe Journal of Organic Chemistry, 1979
- Stoffwechselprodukte von Mikroorganismen. 160. Mitteilung. Conocandin, ein fungistatisches Antibiotikum aus Hormococcus conorum (SACC. et ROUM.) ROBACKHelvetica Chimica Acta, 1976