Nucleophile-Directed Stereocontrol Over Glycosylations Using Geminal-Difluorinated Nucleophiles-Reference-Cited by-同舟云学术

Nucleophile-Directed Stereocontrol Over Glycosylations Using Geminal-Difluorinated Nucleophiles

Published:2016-10-13 Issue:46 Volume:55 Page:14431-14434
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Schumann Benjamin¹²^ORCID,Parameswarappa Sharavathi G.¹^ORCID,Lisboa Marilda P.¹,Kottari Naresh¹,Guidetti Fabio¹,Pereira Claney L.¹^ORCID,Seeberger Peter H.¹²^ORCID

Affiliation:

1. Department of Biomolecular Systems; Max Planck Institute of Colloids and Interfaces; 14424 Potsdam Germany

2. Institute of Chemistry and Biochemistry; Freie Universität Berlin; Arnimallee 22 14195 Berlin Germany

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/anie.201606774/fullpdf

Reference53 articles.

1. Carbohydrate vaccines: developing sweet solutions to sticky situations?

2. Stereocontrolled 1,2-cis glycosylation as the driving force of progress in synthetic carbohydrate chemistry

3. Progress toward developing a carbohydrate-conjugate vaccine against Clostridium difficile ribotype 027: synthesis of the cell-surface polysaccharide PS-I repeating unit

4. Synthesis of conjugation-ready zwitterionic oligosaccharides by chemoselective thioglycoside activation

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