Literature DB >> 28741787

Advances in Stereoselective 1,2-cis Glycosylation using C-2 Auxiliaries.

Rens A Mensink1, Thomas J Boltje1.   

Abstract

The control of stereoselectivity in a glycosylation reaction remains one of the most challenging aspects of oligosaccharide synthesis. Especially the synthesis of 1,2-cis-glycosides is challenging and generally applicable methodology to prepare this linkage is needed to standardize oligosaccharide synthesis. This review highlights the recent development of an elegant strategy employing a C-2 auxiliary to control the anomeric stereoselectivity in glycosylations. The various auxiliaries developed to date, their compatibility with protecting groups and monosaccharide types as well as mechanistic aspects are summarized. Furthermore, the application, advantages and limitations of C-2 auxiliaries in oligosaccharide synthesis are discussed.
© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  chiral auxiliary; glycosylation; oligosaccharides; stereoselectivity; sulfonium ion

Year:  2017        PMID: 28741787     DOI: 10.1002/chem.201700908

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  14 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
Journal:  Chem Rev       Date:  2018-06-28       Impact factor: 60.622

Review 2.  Oligosaccharide Synthesis and Translational Innovation.

Authors:  Larissa Krasnova; Chi-Huey Wong
Journal:  J Am Chem Soc       Date:  2019-02-18       Impact factor: 15.419

3.  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

4.  Stereospecific Furanosylations Catalyzed by Bis-thiourea Hydrogen-Bond Donors.

Authors:  Andrew B Mayfield; Jan B Metternich; Adam H Trotta; Eric N Jacobsen
Journal:  J Am Chem Soc       Date:  2020-02-14       Impact factor: 15.419

Review 5.  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

6.  Halogen-bond-assisted radical activation of glycosyl donors enables mild and stereoconvergent 1,2-cis-glycosylation.

Authors:  Chen Zhang; Hao Zuo; Ga Young Lee; Yike Zou; Qiu-Di Dang; K N Houk; Dawen Niu
Journal:  Nat Chem       Date:  2022-04-11       Impact factor: 24.274

7.  Long-Range Stereodirecting Participation across a Glycosidic Linkage in Glycosylation Reactions.

Authors:  Weizhun Yang; Jicheng Zhang; Chia-Wei Yang; Sherif Ramadan; Richard Staples; Xuefei Huang
Journal:  Org Lett       Date:  2020-12-22       Impact factor: 6.005

8.  Stereocontrolled α-Galactosylation under Cooperative Catalysis.

Authors:  Melanie Shadrick; Yashapal Singh; Alexei V Demchenko
Journal:  J Org Chem       Date:  2020-10-16       Impact factor: 4.354

9.  Direct Experimental Characterization of Glycosyl Cations by Infrared Ion Spectroscopy.

Authors:  Hidde Elferink; Marion E Severijnen; Jonathan Martens; Rens A Mensink; Giel Berden; Jos Oomens; Floris P J T Rutjes; Anouk M Rijs; Thomas J Boltje
Journal:  J Am Chem Soc       Date:  2018-05-07       Impact factor: 15.419

10.  α-Selective Glycosylation with β-Glycosyl Sulfonium Ions Prepared via Intramolecular Alkylation.

Authors:  Sam J Moons; Rens A Mensink; Jeroen P J Bruekers; Maurits L A Vercammen; Laura M Jansen; Thomas J Boltje
Journal:  J Org Chem       Date:  2019-03-07       Impact factor: 4.354

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