Synthesis of Methyl 2,6-Di-N-acetyl-2,3,4,6,7-pentadeoxy-l-lyxo-heptopyranoside, a Derivative of 6-epi-d-Purpurosamine B
- 1 May 1980
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 53 (5) , 1372-1375
- https://doi.org/10.1246/bcsj.53.1372
Abstract
6-epi-d-Purpurosamine B, 2,6-diamino-2,3,4,6,7-pentadeoxy-l-lyxo-heptopyranose, was found to be a component of antibiotic fortimicins. Methyl 2,6-di-N-acetyl-6-epi-α-d-purpurosaminide B has been synthesized from methyl 2-acetamido-2-deoxy-6-O-trityl-α-d-glucopyranoside.This publication has 16 references indexed in Scilit:
- The synthesis of racemic purpurosamine BCarbohydrate Research, 1979
- Fortimicins A and B, new aminoglycoside antibiotics. III. Structural identification.The Journal of Antibiotics, 1977
- Fortimicins A and B, new aminoglycoside antibiotics. II. Isolation, physico-chemical and chromatographic properties.The Journal of Antibiotics, 1977
- Fortimicins A and B, new aminoglycoside antibiotics. I. Producing organism, fermentation a biological properties of fortimicins.The Journal of Antibiotics, 1977
- An approach to the synthesis of branched-chain amino sugars from C-methylene sugarsCarbohydrate Research, 1975
- Syntheses of 3,4-Dideoxy-3-enosides and the Corresponding 3,4-Dideoxy SugarsBulletin of the Chemical Society of Japan, 1971
- Synthesis of N-AcetyllincosamineCHEMICAL & PHARMACEUTICAL BULLETIN, 1970
- heterocyclic amino sugar derivatives Part III. Epimino and oxazolidinone derivatives of 2-amino-2-deoxy-d-alloseCarbohydrate Research, 1969
- Infrared spectra of N-substituted aziridine compoundsAnalytical Chemistry, 1967
- 3,4-Dimethyl-D-glucosamine Hydrochloride and Derivatives1,2Journal of the American Chemical Society, 1952