Literature DB >> 11844489

Efficient intramolecular beta-mannoside formation using m-xylylene and isophthaloyl derivatives as rigid spacers.

Adel A-H Abdel-Rahman1, El Sayed H El Ashry, Richard R Schmidt.   

Abstract

A series of mannosyl donors linked via position 2 to an m-xylylene or an isophthaloyl spacer which was connected to the position 6 of a glucoside acceptor afforded, via intramolecular glycosylation, the corresponding disaccharides with high beta anomeric ratio.

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Year:  2002        PMID: 11844489     DOI: 10.1016/s0008-6215(01)00306-8

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


  6 in total

1.  On the nitrile effect in L-rhamnopyranosylation.

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4.  Glycosyl Thioimidates as Versatile Building Blocks for Organic Synthesis.

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Journal:  Chem Heterocycl Compd (N Y)       Date:  2012-04       Impact factor: 1.277

5.  Dependency of the regio- and stereoselectivity of intramolecular, ring-closing glycosylations upon the ring size.

Authors:  Patrick Claude; Christian Lehmann; Thomas Ziegler
Journal:  Beilstein J Org Chem       Date:  2011-12-01       Impact factor: 2.883

Review 6.  Intramolecular glycosylation.

Authors:  Xiao G Jia; Alexei V Demchenko
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  6 in total

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