Literature DB >> 23674052

O-Benzoxazolyl imidates as versatile glycosyl donors for chemical glycosylation.

Swati S Nigudkar1, Archana R Parameswar, Papapida Pornsuriyasak, Keith J Stine, Alexei V Demchenko.   

Abstract

Herein, we report a new class of glycosyl donors, benzoxazolyl imidates, for chemical glycosylation. The O-benzoxazolyl (OBox) leaving group was designed with an aim to compare the relative reactivity and stability of similarly structured S-benzoxazolyl (SBox) glycosides (thioimidates) developed in our lab and glycosyl trichloroacetimidates (TCAI, O-imidates) developed by Schmidt. Novel OBox donors can be activated under catalytic conditions and provided excellent yields in glycosylation. The OBox imidates were found to be more reactive than either SBox or TCAI donors. The high reactivity profile was confirmed in direct competitive experiments and was found beneficial for HPLC-assisted solid-phase synthesis.

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Year:  2013        PMID: 23674052     DOI: 10.1039/c3ob40667a

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  10 in total

Review 1.  Automated Chemical Oligosaccharide Synthesis: Novel Approach to Traditional Challenges.

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2.  Recent Developments in Stereoselective Chemical Glycosylation.

Authors:  Jesse Ling; Clay S Bennett
Journal:  Asian J Org Chem       Date:  2019-05-02       Impact factor: 3.319

3.  Regenerative Glycosylation.

Authors:  Yashapal Singh; Tinghua Wang; Scott A Geringer; Keith J Stine; Alexei V Demchenko
Journal:  J Org Chem       Date:  2017-12-22       Impact factor: 4.354

4.  Regenerative glycosylation under nucleophilic catalysis.

Authors:  Swati S Nigudkar; Keith J Stine; Alexei V Demchenko
Journal:  J Am Chem Soc       Date:  2014-01-09       Impact factor: 15.419

5.  OFox imidates as versatile glycosyl donors for chemical glycosylation.

Authors:  Swati S Nigudkar; Tinghua Wang; Salvatore G Pistorio; Jagodige P Yasomanee; Keith J Stine; Alexei V Demchenko
Journal:  Org Biomol Chem       Date:  2017-01-04       Impact factor: 3.876

6.  HPLC-Based Automated Synthesis of Glycans in Solution.

Authors:  Samira Escopy; Yashapal Singh; Keith J Stine; Alexei V Demchenko
Journal:  Chemistry       Date:  2022-05-25       Impact factor: 5.020

7.  HPLC-Assisted Automated Oligosaccharide Synthesis: Implementation of the Autosampler as a Mode of the Reagent Delivery.

Authors:  Salvatore G Pistorio; Swati S Nigudkar; Keith J Stine; Alexei V Demchenko
Journal:  J Org Chem       Date:  2016-09-14       Impact factor: 4.354

8.  A Highly Efficient Glycosidation of Glycosyl Chlorides by Using Cooperative Silver(I) Oxide-Triflic Acid Catalysis.

Authors:  Scott A Geringer; Yashapal Singh; Daniel J Hoard; Alexei V Demchenko
Journal:  Chemistry       Date:  2020-06-02       Impact factor: 5.236

9.  Bismuth(iii) triflate as a novel and efficient activator for glycosyl halides.

Authors:  Hayley B Steber; Yashapal Singh; Alexei V Demchenko
Journal:  Org Biomol Chem       Date:  2021-03-24       Impact factor: 3.876

10.  A versatile glycosylation strategy via Au(iii) catalyzed activation of thioglycoside donors.

Authors:  Amol M Vibhute; Arun Dhaka; Vignesh Athiyarath; Kana M Sureshan
Journal:  Chem Sci       Date:  2016-03-08       Impact factor: 9.825

  10 in total

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