Total Synthesis of Streptogramin Antibiotics. (−)-Madumycin II
- 1 January 1996
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 118 (13) , 3303-3304
- https://doi.org/10.1021/ja954312r
Abstract
No abstract availableThis publication has 38 references indexed in Scilit:
- Total Synthesis of (−)-Virginiamycin M2 Using Second-Generation Vinylogous Urethane ChemistryJournal of the American Chemical Society, 1996
- Bioactive sponge peptidesChemical Reviews, 1993
- Ascidians: producers of amino acid-derived metabolitesChemical Reviews, 1993
- Muscarine, oxazole, imidazole, thiazole, and peptide alkaloids and other miscellaneous alkaloidsNatural Product Reports, 1993
- Biosynthesis of antibiotics of the virginiamycin family. 8. Formation of the dehydroproline residueJournal of the American Chemical Society, 1989
- Enantioselective synthesis of the depsipeptide unsaturated acid portion of madumycin IIThe Journal of Organic Chemistry, 1985
- A New Reagent for Activating Carboxyl Groups; Preparation and Reactions ofN,N-Bis[2-oxo-3-ox-azolidinyl]phosphorodiamidic ChlorideSynthesis, 1980
- Interaction of vernamycin A with Escherichia coli ribosomesBiochemistry, 1971
- Virginiamycin M-A specific inhibitor of the acceptor site of ribosomesBiochimie, 1971
- Antibiotics of the ostreogrycin complex. Part II. Structure of ostreogrycin AJournal of the Chemical Society C: Organic, 1966