Literature DB >> 22370177

2-Allylphenyl glycosides as glycosyl donors for sugar coupling.

Shun-Yuan Luo1, Ashish Tripathi, Medel Manuel L Zulueta, Shang-Cheng Hung.   

Abstract

Glycosylations employing 2-allylphenyl glycoside, a new type of stable glycosyl donor, were optimized and explored with a variety of acceptors promoted by ICl/AgOTf. The utility of the protocol was further demonstrated with an efficient synthesis of the disaccharide fragment of bleomycins.
Copyright © 2012 Elsevier Ltd. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22370177     DOI: 10.1016/j.carres.2012.01.022

Source DB:  PubMed          Journal:  Carbohydr Res        ISSN: 0008-6215            Impact factor:   2.104


  3 in total

1.  One-pot anti-Markovnikov hydroamination of unactivated alkenes by hydrozirconation and amination.

Authors:  Alexandra E Strom; John F Hartwig
Journal:  J Org Chem       Date:  2013-08-27       Impact factor: 4.354

2.  Templated Oligosaccharide Synthesis: The Linker Effect on the Stereoselectivity of Glycosylation.

Authors:  Papapida Pornsuriyasak; Xiao G Jia; Sophon Kaeothip; Alexei V Demchenko
Journal:  Org Lett       Date:  2016-04-26       Impact factor: 6.005

Review 3.  Chemical O-Glycosylations: An Overview.

Authors:  Rituparna Das; Balaram Mukhopadhyay
Journal:  ChemistryOpen       Date:  2016-08-17       Impact factor: 2.911

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.