Literature DB >> 11101443

One-pot oligosaccharide synthesis exploiting solvent reactivity effects.

M Lahmann1, S Oscarson.   

Abstract

[reaction: see text] One-pot syntheses of trisaccharides have been accomplished simply by changing the solvent system between the two subsequent glycosylation reactions and utilizing the difference in glycosylation rate between different solvents. By tuning the reactivity of acceptors and donors and performing the first glycosylation in Et(2)O (low glycosylation rate) and the second in CH(2)Cl(2)/Et(2)O (higher glycosylation rate), trisaccharides were synthesized in high yields (76-84%).

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Year:  2000        PMID: 11101443     DOI: 10.1021/ol006621e

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  5 in total

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Authors:  Hemali D Premathilake; Alexei V Demchenko
Journal:  Top Curr Chem       Date:  2011

2.  Iterative one-pot syntheses of chitotetroses.

Authors:  Lijun Huang; Zhen Wang; Xiaoning Li; Xin-shan Ye; Xuefei Huang
Journal:  Carbohydr Res       Date:  2006-01-26       Impact factor: 2.104

3.  Thio-arylglycosides with various aglycon para-substituents: a probe for studying chemical glycosylation reactions.

Authors:  Xiaoning Li; Lijun Huang; Xiche Hu; Xuefei Huang
Journal:  Org Biomol Chem       Date:  2008-10-20       Impact factor: 3.876

4.  Challenges in the Conversion of Manual Processes to Machine-Assisted Syntheses: Activation of Thioglycoside Donors with Aryl(trifluoroethyl)iodonium Triflimide.

Authors:  Regis C Saliba; Zachary J Wooke; Gabriel A Nieves; An-Hsiang Adam Chu; Clay S Bennett; Nicola L B Pohl
Journal:  Org Lett       Date:  2018-01-16       Impact factor: 6.005

5.  Direct, stereoselective thioglycosylation enabled by an organophotoredox radical strategy.

Authors:  Peng Ji; Yueteng Zhang; Feng Gao; Fangchao Bi; Wei Wang
Journal:  Chem Sci       Date:  2020-10-19       Impact factor: 9.825

  5 in total

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