Literature DB >> 26245299

Staudinger Reactions for Selective Functionalization of Polysaccharides: A Review.

Shu Liu1, Kevin J Edgar1.   

Abstract

Staudinger reactions are frequently highly chemoselective and can occur under very mild conditions, so are attractive methods for efficient functionalization of polysaccharides. This review describes recent investigations that exploit Staudinger-related reactions to effectively alter physical and chemical properties of polysaccharides in order to make them more diversely applicable. Staudinger-related reactions, such as Staudinger reduction, Staudinger ligation, and traceless Staudinger ligation comprise a powerful family of techniques enabling preparation of a wide range of polysaccharide derivatives with excellent chemoselectivity and the potential for excellent regioselectivity when combined with other methods. The remarkably mild conditions of the Staudinger reactions, combined with the abiotic nature of the azide group, make these reactions exceptionally attractive for modification of intact biological entities, including living cells.

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Year:  2015        PMID: 26245299     DOI: 10.1021/acs.biomac.5b00855

Source DB:  PubMed          Journal:  Biomacromolecules        ISSN: 1525-7797            Impact factor:   6.988


  7 in total

Review 1.  Phosphine Organocatalysis.

Authors:  Hongchao Guo; Yi Chiao Fan; Zhanhu Sun; Yang Wu; Ohyun Kwon
Journal:  Chem Rev       Date:  2018-09-27       Impact factor: 60.622

Review 2.  Practical Considerations, Challenges, and Limitations of Bioconjugation via Azide-Alkyne Cycloaddition.

Authors:  Chad J Pickens; Stephanie N Johnson; Melissa M Pressnall; Martin A Leon; Cory J Berkland
Journal:  Bioconjug Chem       Date:  2018-02-01       Impact factor: 4.774

3.  Main Group Redox Catalysis of Organopnictogens: Vertical Periodic Trends and Emerging Opportunities in Group 15.

Authors:  Jeffrey M Lipshultz; Gen Li; Alexander T Radosevich
Journal:  J Am Chem Soc       Date:  2021-01-19       Impact factor: 15.419

4.  Total Syntheses of Conjugation-Ready Repeating Units of Acinetobacter baumannii AB5075 for Glycoconjugate Vaccine Development.

Authors:  Shuo Zhang; Peter H Seeberger
Journal:  Chemistry       Date:  2021-11-05       Impact factor: 5.020

Review 5.  Recent Advances in the Chemistry of Glycoconjugate Amphiphiles.

Authors:  Laurent Latxague; Alexandra Gaubert; Philippe Barthélémy
Journal:  Molecules       Date:  2018-01-02       Impact factor: 4.411

6.  An efficient system for bioconjugation based on a widely applicable engineered O-glycosylation tag.

Authors:  Thomas V Murray; Kasia Kozakowska-McDonnell; Adam Tibbles; Annabel Taylor; Daniel Higazi; Emmanuel Rossy; Alessandra Rossi; Sivaneswary Genapathy; Giulia Tamburrino; Nicola Rath; Natalie Tigue; Vivian Lindo; Tristan Vaughan; Monika A Papworth
Journal:  MAbs       Date:  2021 Jan-Dec       Impact factor: 5.857

Review 7.  Biosynthetic Polymers as Functional Materials.

Authors:  Andrea S Carlini; Lisa Adamiak; Nathan C Gianneschi
Journal:  Macromolecules       Date:  2016-06-21       Impact factor: 5.985

  7 in total

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