The total synthesis of the polyether antibiotic X-206
- 1 April 1988
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 110 (8) , 2506-2526
- https://doi.org/10.1021/ja00216a026
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- A stereospecific route to aziridinomitosanes: the synthesis of novel mitomycin congenersJournal of the American Chemical Society, 1985
- Convergent synthesis of polyether ionophore antibiotics: an approach to the synthesis of the monensin tetrahydropyran-bis(tetrahydrofuran) via the ester enolate Claisen rearrangement and reductive decarboxylationJournal of the American Chemical Society, 1985
- Convergent synthesis of polyether ionophore antibiotics: the synthesis of the monensin bis(tetrahydrofuran) via the Claisen rearrangement of an ester enolate with a .beta.-leaving groupJournal of the American Chemical Society, 1985
- Biosynthesis of sulfur compounds. Investigations of the biosynthesis of asparagusic acidJournal of the American Chemical Society, 1985
- A totally synthetic route to lincosamine: some observations on the diastereofacial selectivity of electrophilic reactions on the double bonds of various 5-(1-alkenyl)arabinopyranosidesJournal of the American Chemical Society, 1985
- The total synthesis of ionophore antibiotics. A convergent synthesis of lasalocid A (X537A)Journal of the American Chemical Society, 1983
- Enolate Claisen rearrangement of esters from furanoid and pyranoid glycalsThe Journal of Organic Chemistry, 1980
- Oxidation of long-chain and related alcohols to carbonyls by dimethyl sulfoxide "activated" by oxalyl chlorideThe Journal of Organic Chemistry, 1978
- X-Ray structure of alborixin, a new antibiotic ionophoreJournal of the Chemical Society, Chemical Communications, 1975