2-Substituted fortimicins by ring opening of 2-deoxy-1,2-epimino-2-epi-fortimicin B and by nucleophilic displacements of 2-O-(methylsulfonyl)fortimicin derivatives
- 16 October 1981
- journal article
- Published by Elsevier in Carbohydrate Research
- Vol. 96 (2) , 185-203
- https://doi.org/10.1016/s0008-6215(00)81869-8
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Preparations of 2-epi-fortimicins A from 2-epi-fortimicin B by intramolecular base-catalyzed 2-O-acylation of 1,2′,6′-tri-N-benzyloxycarbonyl-2-epi-fortimicin BCarbohydrate Research, 1981
- 2-epi-fortimicin B. Participation of 1-N-benzyloxycarbonylamino and 1-acetamido groups in solvolysis of 2-O-(methylsulfonyl)fortimicin B derivativesCarbohydrate Research, 1981
- 4-N-acylfortimicins b and the preparation of fortimicin a from fortimicin BCarbohydrate Research, 1980
- Synthesis of 2-deoxyfortimicins and 1-deamino-2-deoxy-2-EPI-aminofortimicins VIA 2-O-methanesulfonylfortimicin B.The Journal of Antibiotics, 1980
- Fortimicins A and B, new aminoglycoside antibiotics. IV. in vitro Study of fortimicin a compared with other aminoglycosides.The Journal of Antibiotics, 1977
- 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