An approach to branched-chain amino sugars, particularly derivatives of l-vancosamine (3-amino-2,3,6-trideoxy-3-C-methyl-l-lyxo-hexose) and its d enantiomer, via the cyanohydrin route-Reference-Cited by-同舟云学术

An approach to branched-chain amino sugars, particularly derivatives of l-vancosamine (3-amino-2,3,6-trideoxy-3-C-methyl-l-lyxo-hexose) and its d enantiomer, via the cyanohydrin route

Published:1982-12 Issue:2 Volume:110 Page:207-215
ISSN:0008-6215
Container-title:Carbohydrate Research
language:en
Short-container-title:Carbohydrate Research

Author:

Brimacombe John S.,Mengech Annalee S.,Rahman Khandker M.M.,Tucker Leslie C.N.

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry

Reference38 articles.

1. The synthesis of some derivatives of l-vancosamine (3-amino-2,3,6-trideoxy-3-C-methyl-l-lyxo-hexose)

2. Chemistry of everninomicin antibiotics. III. Evernitrose, a naturally occurring nitro sugar from everninomicins

3. 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-hexopyranoside

4. The structure of an amino-sugar from the antibiotic vancomycin

5. Vancosamine: the structure and configuration of a novel amino-sugar from vancomycin

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