Protecting carbohydrates with ethers, acetals and orthoesters under basic conditions-Reference-Cited by-同舟云学术

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Protecting carbohydrates with ethers, acetals and orthoesters under basic conditions

Published:2021 Issue:35 Volume:19 Page:7598-7601
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Liang Yang¹,Pedersen Christian M.¹^ORCID

Affiliation:

1. Department of Chemistry, University of Copenhagen, Universitetsparken 5, DK-2100 Copenhagen O, Denmark

Abstract

Chlorinated ethyl and vinyl ethers are introduced at various positions of carbohydrates and gives access to acetals and ortho-esters under basic conditions.

Funder

Chinese Academy of Sciences

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/OB/D1OB01467F

Reference31 articles.

1. A.Lipták , A.Borbás and I.Bajza , 1.06 - Protecting Group Manipulations in Carbohydrate Synthesis , ed. H. Kamerling , Comprehensive Glycoscience, Elsevier , Oxford , 2007 , pp. 203–259

2. Benzyl trichloroacetimidate, a versatile reagent for acid-catalysed benzylation of hydroxy-groups

3. Mix-and-Heat Benzylation of Alcohols Using a Bench-Stable Pyridinium Salt

4. Strategies Toward Protection of 1,2‐ and 1,3‐Diols in Carbohydrate Chemistry

5. An Alternative Preparation of O-Benzylidene Acetals.

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Synthesis and removal of trichloroethylidene derivatives of carbohydrates;Carbohydrate Research;2022-05

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