Literature DB >> 35862424

Broadening the Scope of the Reverse Orthogonal Strategy for Oligosaccharide Synthesis.

Scott A Geringer1, Gustavo A Kashiwagi1,2, Alexei V Demchenko1,2.   

Abstract

The reverse orthogonal strategy was invented in 2011 in an attempt to address drawbacks of other strategies for glycan assembly. Different from the classical orthogonal approach that relies on the orthogonality of leaving groups, the reverse strategy is based on orthogonal protecting groups that could be removed during the glycosylation step. This strategy remained largely unexplored due to only one combination of orthogonal protecting groups that would fit into this concept. Reported herein are new orthogonal combinations of leaving and protecting groups that help to streamline the glycan assembly. Also reported is further refinement of the previously reported reaction conditions.

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Year:  2022        PMID: 35862424      PMCID: PMC9402073          DOI: 10.1021/acs.joc.2c00905

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.198


  21 in total

1.  Efficient solid-phase synthesis of a complex, branched N-glycan hexasaccharide: use of a novel linker and temporary-protecting-group pattern.

Authors:  Xiangyang Wu; Matthias Grathwohl; Richard R Schmidt
Journal:  Angew Chem Int Ed Engl       Date:  2002-12-02       Impact factor: 15.336

Review 2.  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

3.  Iron(iii) chloride-catalyzed activation of glycosyl chlorides.

Authors:  Scott A Geringer; Alexei V Demchenko
Journal:  Org Biomol Chem       Date:  2018-12-05       Impact factor: 3.876

4.  Automated polysaccharide synthesis: assembly of a 30mer mannoside.

Authors:  Oliviana Calin; Steffen Eller; Peter H Seeberger
Journal:  Angew Chem Int Ed Engl       Date:  2013-04-22       Impact factor: 15.336

5.  A highly convergent synthesis of a complex oligosaccharide derived from group B type III Streptococcus.

Authors:  A V Demchenko; G J Boons
Journal:  J Org Chem       Date:  2001-04-20       Impact factor: 4.354

6.  (2-Nitrophenyl)acetyl: a new, selectively removable hydroxyl protecting group.

Authors:  Katalin Daragics; Péter Fügedi
Journal:  Org Lett       Date:  2010-05-07       Impact factor: 6.005

7.  Synthesis of β-Glucosides with 3-O-Picoloyl-Protected Glycosyl Donors in the Presence of Excess Triflic Acid: A Mechanistic Study.

Authors:  Michael P Mannino; Alexei V Demchenko
Journal:  Chemistry       Date:  2020-01-31       Impact factor: 5.236

8.  Linear synthesis of a protected H-type II pentasaccharide using glycosyl phosphate building blocks.

Authors:  K R Love; R B Andrade; P H Seeberger
Journal:  J Org Chem       Date:  2001-11-30       Impact factor: 4.354

9.  Glycosyl alkoxythioimidates as complementary building blocks for chemical glycosylation.

Authors:  Sneha C Ranade; Sophon Kaeothip; Alexei V Demchenko
Journal:  Org Lett       Date:  2010-11-18       Impact factor: 6.005

10.  Regioselective one-pot protection, protection-glycosylation and protection-glycosylation-glycosylation of carbohydrates: a case study with D-glucose.

Authors:  Teng-Yi Huang; Medel Manuel L Zulueta; Shang-Cheng Hung
Journal:  Org Biomol Chem       Date:  2014-01-14       Impact factor: 3.876

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