Synthetic Studies of Rifamycins. V. A Chiral Synthesis of an Ansa-chain Compound for the C-17–C-29 Portion of Rifamycin W
- 1 October 1982
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 55 (10), 3283-3296
- https://doi.org/10.1246/bcsj.55.3283
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- Synthetic Studies of Rifamycins. III. The Partial Synthesis of Rifamycin Ansa-chain Compounds from Their Degradation ProductsBulletin of the Chemical Society of Japan, 1981
- Further synthetic studies on rifamycin sTetrahedron, 1981
- Synthetic Studies of Rifamycins. II. Syntheses of Methyl 2,4,6,7-Tetradeoxy-4-C-methyl-3-O-methyl-α-l-arabino-heptopyranosid-6-ulose and Its Derivatives Utilizable in the Construction of the Rifamycin Ansa Chain PortionBulletin of the Chemical Society of Japan, 1980
- Early intermediates in the biosynthesis of ansamycins. III. Isolation and identification of further 8-deoxyansamycins of the rifamycin-type.The Journal of Antibiotics, 1980
- Early intermediates in the biosynthesis of ansamycins. II. Isolation and identification of proasamycin B-M1 and protorifamycin I-M1.The Journal of Antibiotics, 1979
- Early intermediates in the biosynthesis of ansamycins. I. Isolation and identification of protorifamycin I.The Journal of Antibiotics, 1978
- Structure of rifamycin WTetrahedron, 1974
- Rifamycin Biosynthesis Studied with 13C Enriched Precursors and Carbon Magnetic ResonanceNature, 1973
- The synthesis of branched-chain, deoxy sugars by sugar epoxide-grignard reagent reactionsCarbohydrate Research, 1970
- Studies in Stereochemistry. X. The Rule of “Steric Control of Asymmetric Induction” in the Syntheses of Acyclic SystemsJournal of the American Chemical Society, 1952