Literature DB >> 29805297

Pre-activation Based Stereoselective Glycosylations.

Bo Yang1, Weizhun Yang1, Sherif Ramadan1,2, Xuefei Huang1,3,4.   

Abstract

Due to the wide presence of carbohydrates in nature and their crucial roles in numerous important biological processes, oligosaccharides have attracted a lot of attention in synthetic organic chemistry community. Many innovative synthetic methods have been developed for oligosaccharide synthesis, among which the pre-activation based glycosylation is particularly noteworthy. Traditionally, glycosylation reactions are carried out when the glycosyl donor and the acceptor are both present when the promoter is added. In comparison, the pre-activation based glycosylation is unique, where the glycosyl donor is activated by the promoter in the absence of the acceptor. Upon complete donor activation, the acceptor is added to the reaction mixture enabling glycosylation. The key step in any oligosaccharide synthesis is the stereoselective formation of the glycosidic bond. As donor activation and acceptor glycosylation are temporally separated, pre-activation based glycosylation can bestow unique stereochemical control. This review systematically discusses factors impacting the stereochemical outcome of a pre-activation based glycosylation reaction including substituents on the glycosyl donor, reaction solvent, and additives. Applications of pre-activation based stereoselective glycosylation in assembly of complex oligosaccharides are also discussed.

Entities:  

Keywords:  diastereoselectivity; glycosides; glycosylation; pre-activation; synthesis design

Year:  2017        PMID: 29805297      PMCID: PMC5963711          DOI: 10.1002/ejoc.201701579

Source DB:  PubMed          Journal:  European J Org Chem        ISSN: 1099-0690


  84 in total

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Journal:  Angew Chem Int Ed Engl       Date:  2005-01-28       Impact factor: 15.336

3.  Dimethylformamide: an unusual glycosylation modulator.

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Journal:  Angew Chem Int Ed Engl       Date:  2011-06-17       Impact factor: 15.336

4.  Highly efficient syntheses of hyaluronic acid oligosaccharides.

Authors:  Lijun Huang; Xuefei Huang
Journal:  Chemistry       Date:  2007       Impact factor: 5.236

5.  Stereoelectronic effects determine oxacarbenium vs β-sulfonium ion mediated glycosylations.

Authors:  Thomas J Boltje; Jin-Hwan Kim; Jin Park; Geert-Jan Boons
Journal:  Org Lett       Date:  2010-12-15       Impact factor: 6.005

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Journal:  ACS Med Chem Lett       Date:  2010-07-12       Impact factor: 4.345

7.  β-Selective Glucosylation in the Absence of Neighboring Group Participation: Influence of the 3,4-O-Bisacetal Protecting System.

Authors:  David Crich; Venkataraman Subramanian; Thomas K Hutton
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8.  Evidence for endocyclic cleavage of conformationally restricted glycopyranosides.

Authors:  Shino Manabe; Kazuyuki Ishii; Daisuke Hashizume; Hiroyuki Koshino; Yukishige Ito
Journal:  Chemistry       Date:  2009-07-13       Impact factor: 5.236

9.  Does neighboring group participation by non-vicinal esters play a role in glycosylation reactions? Effective probes for the detection of bridging intermediates.

Authors:  David Crich; Tianshun Hu; Feng Cai
Journal:  J Org Chem       Date:  2008-10-22       Impact factor: 4.354

10.  Determination of the Influence of Side-Chain Conformation on Glycosylation Selectivity using Conformationally Restricted Donors.

Authors:  Suresh Dharuman; David Crich
Journal:  Chemistry       Date:  2016-02-16       Impact factor: 5.236

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  7 in total

Review 1.  Automated Chemical Oligosaccharide Synthesis: Novel Approach to Traditional Challenges.

Authors:  Matteo Panza; Salvatore G Pistorio; Keith J Stine; Alexei V Demchenko
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2.  Mechanisms of Stereodirecting Participation and Ester Migration from Near and Far in Glycosylation and Related Reactions.

Authors:  Asiri A Hettikankanamalage; Robert Lassfolk; Filip S Ekholm; Reko Leino; David Crich
Journal:  Chem Rev       Date:  2020-07-05       Impact factor: 60.622

3.  The Cyclic Nitronate Route to Pharmaceutical Molecules: Synthesis of GSK's Potent PDE4 Inhibitor as a Case Study.

Authors:  Evgeny V Pospelov; Ivan S Golovanov; Sema L Ioffe; Alexey Yu Sukhorukov
Journal:  Molecules       Date:  2020-08-08       Impact factor: 4.411

Review 4.  Recent Advances in Stereoselective Chemical O-Glycosylation Reactions.

Authors:  Mana Mohan Mukherjee; Rina Ghosh; John A Hanover
Journal:  Front Mol Biosci       Date:  2022-06-14

5.  Highly reactive 2-deoxy-2-iodo-d-allo and d-gulo pyranosyl sulfoxide donors ensure β-stereoselective glycosylations with steroidal aglycones.

Authors:  Jordi Mestre; David Collado; David Benito-Alifonso; Miguel A Rodríguez; M Isabel Matheu; Yolanda Díaz; Sergio Castillón; Omar Boutureira
Journal:  RSC Adv       Date:  2018-08-24       Impact factor: 4.036

6.  Ferrocenium complex aided O-glycosylation of glycosyl halides.

Authors:  Deva Saroja Talasila; Eike B Bauer
Journal:  RSC Adv       Date:  2021-11-17       Impact factor: 4.036

7.  A Streamlined Regenerative Glycosylation Reaction: Direct, Acid-Free Activation of Thioglycosides.

Authors:  Samira Escopy; Yashapal Singh; Keith J Stine; Alexei V Demchenko
Journal:  Chemistry       Date:  2020-11-30       Impact factor: 5.236

  7 in total

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