Synthesis of 2,3,6-trideoxy-3-C-methyl-4-O-methyl-3-nitro-l-xylo-hexopyranose (l-rubranitrose)
- 1 August 1982
- journal article
- research article
- Published by Elsevier in Carbohydrate Research
- Vol. 106 (1) , C1-C3
- https://doi.org/10.1016/s0008-6215(00)80745-4
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Kijanimicin. 1. Structures of the individual sugar componentsJournal of the American Chemical Society, 1981
- An approach to the construction of the aromatic portions of naphthomycin and the rubradirins - nucleophilic additions to unsymmetrically substituted naphthoquinonesTetrahedron Letters, 1980
- The synthesis of evernitrose and 3-epi-evernitroseCarbohydrate Research, 1979
- The chemistry of rubradirin. II. Rubranitrose.The Journal of Antibiotics, 1979
- The chemistry of the rubradirins. I. The structures of rubransarols A and B.The Journal of Antibiotics, 1978
- Stereochemistry at C-3 of evernitrose: a fallacy in the determination of stereochemistry at quaternary centres using nuclear magnetic resonance spectroscopy. X-Ray crystal structure of methyl 3-acetamido-2,3,6-trideoxy-3-c,4-O-dimethyl-L-xylo-hexopyranosideJournal of the Chemical Society, Chemical Communications, 1977
- Rubradirin, an inhibitor of ribosomal polypeptide biosynthesisBiochemistry, 1973
- Synthesis of branched-chain sugars by the wittig reactionCanadian Journal of Chemistry, 1968