A concise and stereoselective route to the predominant stereochemical pattern of the tetrahydropyranoid antibiotics: an application to indanomycin
- 1 April 1987
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 109 (7) , 2082-2089
- https://doi.org/10.1021/ja00241a028
Abstract
No abstract availableThis publication has 2 references indexed in Scilit:
- 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
- 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