Side reactions with 2,2,2-trichloroethoxysulfates during the synthesis of glycans-Reference-Cited by-同舟云学术

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Side reactions with 2,2,2-trichloroethoxysulfates during the synthesis of glycans

Published:2014-09 Issue: Volume:396 Page:14-24
ISSN:0008-6215
Container-title:Carbohydrate Research
language:en
Short-container-title:Carbohydrate Research

Author:

Matsushita Kenya,Sato Yuta,Funamoto Shinji,Tamura Jun-ichi

Funder

Otsuka Chemical Co., Ltd

Otsuka Pharmaceutical Co., Ltd

MEXT

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry

Reference23 articles.

1. A method for the sulfation of sugars, employing a stable, aryl sulfate intermediate

2. Reactions of phenyl chlorosulfate at OH-2 and OH-3 of aldohexopyranose derivatives. Competing substitution and displacement reactions

3. A Comprehensive Approach to the Synthesis of Sulfate Esters

4. Trifluoroethylsulfonate protected monosaccharides in glycosylation reactions

5. Synthesis and Protection of Aryl Sulfates Using the 2,2,2-Trichloroethyl Moiety

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1. Borane–Trimethylamine Complex: A Versatile Reagent in Organic Synthesis;Molecules;2024-04-27

2. A General Approach to O ‐Sulfation by a Sulfur(VI) Fluoride Exchange Reaction;Angewandte Chemie International Edition;2020-08-20

3. A General Approach to O ‐Sulfation by a Sulfur(VI) Fluoride Exchange Reaction;Angewandte Chemie;2020-08-20

4. Chemical synthesis of human syndecan-4 glycopeptide bearing O-, N-sulfation and multiple aspartic acids for probing impacts of the glycan chain and the core peptide on biological functions;Chemical Science;2020

5. The application of 2,2,2-trichloroethyl sulfate to the synthesis of chondroitin sulfate C and D;Carbohydrate Research;2015-04

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