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Synthesis of methyl 2,3,6-trideoxy- -L-erythro-hexopyranoside (methyl -L-amicetoside) and methyl 2,3,4,6-tetradeoxy-4-(dimethylamino)- -L-threo-hexopyranoside (methyl -L-ossaminide). 1972

J S Brimacombe, and L W Doner, and A J Rollins

UI MeSH Term Description Entries
D008722 Methods A series of steps taken in order to conduct research. Techniques,Methodological Studies,Methodological Study,Procedures,Studies, Methodological,Study, Methodological,Method,Procedure,Technique
D008744 Methylamines Derivatives of methylamine (the structural formula CH3NH2).
D011714 Pyrans Pyran
D006027 Glycosides Any compound that contains a constituent sugar, in which the hydroxyl group attached to the first carbon is substituted by an alcoholic, phenolic, or other group. They are named specifically for the sugar contained, such as glucoside (glucose), pentoside (pentose), fructoside (fructose), etc. Upon hydrolysis, a sugar and nonsugar component (aglycone) are formed. (From Dorland, 28th ed; From Miall's Dictionary of Chemistry, 5th ed) Glycoside
D006595 Hexosamines AMINO SUGARS created by adding an amine group to a hexose sugar. Hexosamine
D000900 Anti-Bacterial Agents Substances that inhibit the growth or reproduction of BACTERIA. Anti-Bacterial Agent,Anti-Bacterial Compound,Anti-Mycobacterial Agent,Antibacterial Agent,Antibiotics,Antimycobacterial Agent,Bacteriocidal Agent,Bacteriocide,Anti-Bacterial Compounds,Anti-Mycobacterial Agents,Antibacterial Agents,Antibiotic,Antimycobacterial Agents,Bacteriocidal Agents,Bacteriocides,Agent, Anti-Bacterial,Agent, Anti-Mycobacterial,Agent, Antibacterial,Agent, Antimycobacterial,Agent, Bacteriocidal,Agents, Anti-Bacterial,Agents, Anti-Mycobacterial,Agents, Antibacterial,Agents, Antimycobacterial,Agents, Bacteriocidal,Anti Bacterial Agent,Anti Bacterial Agents,Anti Bacterial Compound,Anti Bacterial Compounds,Anti Mycobacterial Agent,Anti Mycobacterial Agents,Compound, Anti-Bacterial,Compounds, Anti-Bacterial
D001386 Azides Organic or inorganic compounds that contain the -N3 group. Azide

Related Publications

J S Brimacombe, and L W Doner, and A J Rollins
A synthesis of methyl 2,3,6-trideoxy-alpha-D-erythro-hexopyranoside (methyl alpha-amicetoside).
November 1969, The Journal of organic chemistry,
J S Brimacombe, and L W Doner, and A J Rollins
Synthesis of derivatives of 3-amino-2,3,4,6-tetradeoxy-L-threo-hexose (4-deoxydaunosamine) and its L-erythro isomer.
December 1979, Carbohydrate research,
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The synthesis of methyl 3-amino-2,3,6-trideoxy-alpha-L-arabino-hexopyranoside, a structural analog of duanosamine.
November 1974, Carbohydrate research,
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Synthesis of 6-azido- and 6-amino-2,3,6-trideoxy-D-erythro-hexose.
July 1977, Carbohydrate research,
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Alternative preparation of methyl 3-amino-2,3,6-trideoxy-alpha-D-arabino-hexopyranoside and chiral intermediates for the synthesis of thienamycin.
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Synthesis, the crystal structure, and high-resolution NMR spectroscopy of methyl 4-O-acetyl-3-azido-2,3,6-trideoxy-6-iodo-alpha-D-arabino-hexopyranoside.
February 2002, Carbohydrate research,
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Synthesis and conformational studies on methyl 4-O-acetyl-3-azido-2,3,6-trideoxy-hex-5-enopyranosides of the L series.
September 2005, Carbohydrate research,
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[Synthetic studies in the series of polyene macrolide antibiotics. 5. Synthesis of methyl-2,4,6-trideoxy-2,4-di-C-methyl-alpha-L- gluco-hexopyranoside and methyl-2,4,6-trideoxy-2,4-di-C-methyl- alpha-L-manno-hexopyranoside, the stereoisomers of the C33-C38 fragment of amphotericin B].
August 1988, Bioorganicheskaia khimiia,
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Design, synthesis and biological activity of 7-O-(4-O-acetyl-3-iodo-2,3,6-trideoxy-alpha-L-arabino-hexopyranosyl) daunomycinone and 7-O-(3-chloro-2,3,6-trideoxy-4-O-propanoyl-alpha-L-lyxo- hexopyranosyl)daunomycinone.
January 2000, Chemical & pharmaceutical bulletin,
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Methyl 3-amino-2,3,6,-trideoxy-L-hexopyranosides in DFT level theory conformational studies.
July 2008, The journal of physical chemistry. A,
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