Synthesis of a Lividomycin B Analogue, 5-O-[3-O-(2-Amino-2-deoxy-α-d-grlucopyranosyl)-β-d-ribofuranosyl]-3′-deoxyparomamine
- 1 September 1977
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 50 (9) , 2369-2374
- https://doi.org/10.1246/bcsj.50.2369
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Deneosaminyllividomycin B.The Journal of Antibiotics, 1977
- Synthesis of Butirosin B and Its 3′,4′-Dideoxy DerivativeBulletin of the Chemical Society of Japan, 1974
- CHEMICAL CONVERSION OF LIVIDOMYCIN A INTO LIVIDOMYCIN BThe Journal of Antibiotics, 1972
- SYNTHESIS OF PAROMAMINEThe Journal of Antibiotics, 1972
- Synthesis of Cyclic α-Amino Acids. IV. Syntheses of Adenine Nucleosides of 3-Amino-3-C-carboxy-3-deoxy-d-ribofuranose and 3-Amino-3-C-carboxy-3-deoxy-d-ribopyranoseBulletin of the Chemical Society of Japan, 1970
- Synthesis of D-Ribose from D-XyloseYAKUGAKU ZASSHI, 1963
- THE CONFIGURATION OF GLYCOSIDIC LINKAGES IN OLIGOSACCHARIDES: X. KÖNIGS–KNORR REACTIONS OF 3,5-DI-O-BENZOYL-ARABINO- AND -RIBO-FURANOSYL BROMIDES AND THEIR 2-SUBSTITUTED DERIVATIVESCanadian Journal of Chemistry, 1962
- New Method of Removing Xanthate Groups from Carbohydrates. Chemical Structure of Methyl α-D-Glucopyranoside Monoxanthate1Journal of the American Chemical Society, 1960
- Über GlucosaminideEuropean Journal of Inorganic Chemistry, 1960