The biosynthesis of furanomycin. Mechanism of formation of the ether linkage
- 1 June 1988
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 110 (12) , 4035-4036
- https://doi.org/10.1021/ja00220a051
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Steric course of the allylic rearrangement catalyzed by .beta.-hydroxydecanoylthioester dehydrase. Mechanistic implicationsJournal of the American Chemical Society, 1984
- Polyether biosynthesis. 2. Origin of the oxygen atoms of monensin AJournal of the American Chemical Society, 1982
- Total synthesis of (+)-furanomycin and stereoisomersJournal of the American Chemical Society, 1980
- Studies of enzyme-mediated reactions. Part VII. Stereospecific syntheses of tritium-labelled (2R)- and (2S)-dopamines: stereochemical course of hydroxylation of dopamine by dopamine β-hydroxylase (E.C. 1.14.17.1)Journal of the Chemical Society, Perkin Transactions 1, 1976
- A New Antibiotic. Furanomycin, an Isoleucine AntagonistJournal of Medicinal Chemistry, 1967