Synthesis of 2-deoxy-2-[(3R)-3-hydroxytetradecanamido]-3-O-[(3R)-3-hydroxytetradecanyl]-α-d-glucopyranosyl dihydrogen phosphate and 2-deoxy-2-[(3R)-3-hydroxy-tetradecanamido]-3-O-[3R)-3-hydroxytetradecanyl]-4-O-phosphono-d-glucopyranose-Reference-Cited by-同舟云学术

Synthesis of 2-deoxy-2-[(3R)-3-hydroxytetradecanamido]-3-O-[(3R)-3-hydroxytetradecanyl]-α-d-glucopyranosyl dihydrogen phosphate and 2-deoxy-2-[(3R)-3-hydroxy-tetradecanamido]-3-O-[3R)-3-hydroxytetradecanyl]-4-O-phosphono-d-glucopyranose

Published:1991-12 Issue: Volume:222 Page:57-68
ISSN:0008-6215
Container-title:Carbohydrate Research
language:en
Short-container-title:Carbohydrate Research

Author:

Shiozaki Masao,Kobayashi Yoshiyuki,Ishida Noboru,Arai Masami,Hiraoka Tetsuo,Nishijima Masahiro,Kuge Sayuri,Otsuka Toshiaki,Akamatsu Yuzuru

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry

Reference17 articles.

1. Chemische Erforschung von Lipopolysacchariden gramnegativer Bakterien

2. Total synthesis of escherichia coli lipid A

3. New development of a common glucosamine disaccharide intermediate with chemically differentiated two amino and six hydroxyl groups for lipid a syntheses and a formal synthesis of Salmonella mutant lipid A.

4. Membrane lipid biogenesis in Escherichia coli: identification of genetic loci for phosphatidylglycerophosphate synthetase and construction of mutants lacking phosphatidylglycerol.

5. Synthesis of the optically active 4-O-phosphono-d-glucosamine derivatives related to the nonreducing-sugar subunit of bacterial lipid A

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