Chemical synthesis of 3-amino-2,3-dideoxy-d-myo-inositol (an intermediate in the biosynthesis of 2-deoxystreptamine) and its d-epi stereoisomer
- 15 November 1986
- journal article
- research article
- Published by Elsevier in Carbohydrate Research
- Vol. 156, 247-255
- https://doi.org/10.1016/s0008-6215(00)90119-8
Abstract
No abstract availableThis publication has 22 references indexed in Scilit:
- Biosynthesis of 2-deoxystreptamine.The Journal of Antibiotics, 1985
- Biosynthetic pathway of 2-deoxystreptamine.The Journal of Antibiotics, 1981
- Synthesis of (1D)-1,3,5/2,4- and (1L)-1,2,4/3,5-5-aminocyclohexanetetrols.The Journal of Antibiotics, 1981
- Structure elucidation of an intermediate of 2-deoxystreptamine biosynthesis.The Journal of Antibiotics, 1980
- Accumulation of 2-deoxy-scyllo-inosamine by a 2-deoxystreptamine-requiring idiotroph of Micromonospora sagamiensis.The Journal of Antibiotics, 1980
- Isolation of an intermediate of 2-deoxystreptamine biosynthesis from a mutant of Bacillus circulans.The Journal of Antibiotics, 1980
- Biosynthesis of butirosins. II. Biosynthetic pathway of butirosins elucidated from cosynthesis and feeding experiments.The Journal of Antibiotics, 1979
- Mutational biosynthesis by idiotrophs of Micromonospora purpurea. II. Conversion of non-amino containing cyclitols to aminoglycoside antibiotics.The Journal of Antibiotics, 1977
- Biosynthesis of aminocyclitol antibiotics.The Journal of Antibiotics, 1976
- Carbon-13 as a biosynthetic tool. IV. Biosynthetic incorporation of glucosamine-1-13C and glucose-6-13C into neomycinJournal of the American Chemical Society, 1974