A highly stereocontrolled route to the monensin spiroketal ring system
- 1 March 1988
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 53 (5) , 1046-1056
- https://doi.org/10.1021/jo00240a022
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- Sodium ion-proton exchange reactions of the carboxylic acid ionophore monensinJournal 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
- Convergent synthesis of polyether ionophore antibiotics: the synthesis of the monensin spiroketalJournal of the American Chemical Society, 1985
- Synthetic studies toward aflavinine: a synthesis of 3-demethylaflavinine via a [2 + 2 + 2] annulationJournal of the American Chemical Society, 1985
- Rates and equilibria of alkali metal and silver ion complex formation with monensin in ethanolJournal of the American Chemical Society, 1984
- Stability constants of complexes of monensin and lasalocid with alkali-metal and alkaline-earth-metal ions in protic and polar aprotic solventsJournal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases, 1984
- Polyether biosynthesis. 2. Origin of the oxygen atoms of monensin AJournal of the American Chemical Society, 1982
- Complexation of metal ions by monensin. Crystal and molecular structure of hydrated and anhydrous crystal forms of sodium monensinJournal of the American Chemical Society, 1980
- Oxidation of long-chain and related alcohols to carbonyls by dimethyl sulfoxide "activated" by oxalyl chlorideThe Journal of Organic Chemistry, 1978