Synthesis of α-Manp-(1→2)-α-Manp-(1→3)-α-Manp-(1→3)-Manp, the tetrasaccharide repeating unit of Escherichia coli O9a, and α-Manp-(1→2)-α-Manp-(1→2)-α-Manp-(1→3)-α-Manp-(1→3)-Manp, the pentasaccharide repeating unit of E. coli O9 and Klebsiella O3-Reference-Cited by-同舟云学术

Synthesis of α-Manp-(1→2)-α-Manp-(1→3)-α-Manp-(1→3)-Manp, the tetrasaccharide repeating unit of Escherichia coli O9a, and α-Manp-(1→2)-α-Manp-(1→2)-α-Manp-(1→3)-α-Manp-(1→3)-Manp, the pentasaccharide repeating unit of E. coli O9 and Klebsiella O3

Published:2002-03 Issue:5 Volume:337 Page:383-390
ISSN:0008-6215
Container-title:Carbohydrate Research
language:en
Short-container-title:Carbohydrate Research

Author:

Chen Langqiu,Zhu Yuliang,Kong Fanzuo

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry

Reference11 articles.

1. A Single Amino Acid Substitution in a Mannosyltransferase, WbdA, Converts the Escherichia coli O9 Polysaccharide into O9a: Generation of a New O-Serotype Group

2. A highly stereoselective and practical synthesis of cyclomannohexaose, Cyclo{→4)-[α-d-Manp-(1→4)-]5-α-d-Manp-(1→}, a manno isomer of cyclomaltohexaose

3. Über die Verseifung acetylierter Zucker und verwandter Substanzen

4. Selective 3-O-allylation and 3-O-benzylation of methyl α-d-manno-, α-l-rhamno- and β-l-fuco-pyranoside

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