Literature DB >> 21229347

Effect of electron-withdrawing protecting groups at remote positions of donors on glycosylation stereochemistry.

Kwan Soo Kim1, Dae-Hwan Suk.   

Abstract

Here we review the equatorial β-directing effects of electron-withdrawing protecting groups at remote positions of mannopyranosyl donors, mannuronate donors, rhamnopyranosyl donors, and 2,6-dideoxyglucopyranosyl donors. We discuss the equatorial α-directing effect of an electron-withdrawing group at the N-5 position of sialyl donors. The proposed mechanism and origin of some of the equatorial β-directing effects are described. We also review the effects of potentially participating, electron-withdrawing protecting groups at remote positions of glycopyranosyl and glycofuranosyl donors on the glycosylation stereochemistries. Further, we present substantial evidence in favor of the remote participation by the electron-withdrawing protecting groups and also include reports that are opposed to remote participation.

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Year:  2011        PMID: 21229347     DOI: 10.1007/128_2010_107

Source DB:  PubMed          Journal:  Top Curr Chem        ISSN: 0340-1022


  13 in total

1.  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

2.  Methodology development and physical organic chemistry: a powerful combination for the advancement of glycochemistry.

Authors:  David Crich
Journal:  J Org Chem       Date:  2011-10-04       Impact factor: 4.354

3.  Dissecting the influence of oxazolidinones and cyclic carbonates in sialic acid chemistry.

Authors:  Pavan K Kancharla; Chandrasekhar Navuluri; David Crich
Journal:  Angew Chem Int Ed Engl       Date:  2012-09-13       Impact factor: 15.336

4.  Automated Solution-Phase Synthesis of S-Glycosides for the Production of Oligomannopyranoside Derivatives.

Authors:  Mallory K Kern; Nicola L B Pohl
Journal:  Org Lett       Date:  2020-05-20       Impact factor: 6.005

5.  Cation Clock Reactions for the Determination of Relative Reaction Kinetics in Glycosylation Reactions: Applications to Gluco- and Mannopyranosyl Sulfoxide and Trichloroacetimidate Type Donors.

Authors:  Philip O Adero; Takayuki Furukawa; Min Huang; Debaraj Mukherjee; Pascal Retailleau; Luis Bohé; David Crich
Journal:  J Am Chem Soc       Date:  2015-08-07       Impact factor: 15.419

6.  Oxidative Deamination of N-Acetyl Neuraminic Acid: Substituent Effects and Mechanism.

Authors:  Szymon Buda; David Crich
Journal:  J Am Chem Soc       Date:  2016-01-15       Impact factor: 15.419

7.  Probing the influence of a 4,6-O-acetal on the reactivity of galactopyranosyl donors: verification of the disarming influence of the trans-gauche conformation of C5-C6 bonds.

Authors:  Myriame Moumé-Pymbock; Takayuki Furukawa; Sujit Mondal; David Crich
Journal:  J Am Chem Soc       Date:  2013-09-11       Impact factor: 15.419

8.  Influence of side chain conformation and configuration on glycosyl donor reactivity and selectivity as illustrated by sialic acid donors epimeric at the 7-position.

Authors:  Pavan K Kancharla; David Crich
Journal:  J Am Chem Soc       Date:  2013-12-09       Impact factor: 15.419

9.  Absence of Stereodirecting Participation by 2-O-Alkoxycarbonylmethyl Ethers in 4,6-O-Benzylidene-Directed Mannosylation.

Authors:  Peng Wen; David Crich
Journal:  J Org Chem       Date:  2015-11-25       Impact factor: 4.354

10.  Synthesis of Conformationally-Locked cis- and trans-Bicyclo[4.4.0] Mono-, Di-, and Trioxadecane Modifications of Galacto- and Glucopyranose; Experimental Limiting 3JH,H Coupling Constants for the Estimation of Carbohydrate Side Chain Populations and Beyond.

Authors:  Harsha Amarasekara; Suresh Dharuman; Takayuki Kato; David Crich
Journal:  J Org Chem       Date:  2018-01-03       Impact factor: 4.354

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