A synthesis of a common intermediate to the lactone–pyrrolidinone ring systems in oxazolomycin A and neooxazolomycin
- 1 July 2007
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 63 (27) , 6216-6231
- https://doi.org/10.1016/j.tet.2007.03.043
Abstract
No abstract availableKeywords
This publication has 72 references indexed in Scilit:
- Lajollamycin, a Nitro-tetraene Spiro-β-lactone-γ-lactam Antibiotic from the Marine Actinomycete Streptomyces nodosusJournal of Natural Products, 2005
- Absolute stereochemistry determination of 16-methyloxazolomycin produced by a Streptomyces sp.The Journal of Antibiotics, 1999
- Novel Bioactive Oxazolomycin Isomers Produced by Streptomyces albus JA3453.Bioscience, Biotechnology, and Biochemistry, 1998
- 16-Methyloxazolomycin, a New Antimicrobial and Cytotoxic Substance Produced by a Streptomyces sp.The Journal of Antibiotics, 1997
- Oxazolomycin Esters, Specific Inhibitors of Plant TransformationBioscience, Biotechnology, and Biochemistry, 1992
- Inhibitory effect of oxazolomycin on crown gall formation.Agricultural and Biological Chemistry, 1989
- Structure of oxazolomycin, a novel β-lactone antibioticTetrahedron Letters, 1985
- Isolation and structural determination of a new antibiotic curromycin B.Agricultural and Biological Chemistry, 1985
- Structure of a new antibiotic curromycin A produced by a genetically modified strain of Streptomyces hygroscopicus, a polyether antibiotic producing organism.The Journal of Antibiotics, 1985
- Structure of neooxazolomycin, an antitumor antibioticTetrahedron Letters, 1985