Literature DB >> 28617506

A flexible 1,2-cis α-glycosylation strategy based on in situ adduct transformation.

Jhe-Cyuan Hu1, Ai-Fen Wendy Feng, Bo-Yao Chang, Chun-Hung Lin, Kwok-Kong Tony Mong.   

Abstract

A flexible 1,2-cis α-selective glycosylation strategy for a wide range of glycosyl donors and acceptors has been developed, which is based on an in situ adduct transformation protocol. Based on this strategy, both NFM-derived and iodide covalent adducts can be accessed for glycosylation. Using low temperature NMR spectroscopy, the aforementioned glycosyl adducts were detected.

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Year:  2017        PMID： 28617506     DOI： 10.1039/c7ob00839b

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


  3 in total

Review 1.  The Experimental Evidence in Support of Glycosylation Mechanisms at the SN1-SN2 Interface.

Authors:  Philip Ouma Adero; Harsha Amarasekara; Peng Wen; Luis Bohé; David Crich
Journal:  Chem Rev       Date:  2018-05-30       Impact factor: 60.622

2.  Synthesis of Gentamicin Minor Components: Gentamicin B1 and Gentamicin X2.

Authors:  Parasuraman Rajasekaran; David Crich
Journal:  Org Lett       Date:  2020-04-28       Impact factor: 6.005

3.  Reagent Controlled Stereoselective Synthesis of α-Glucans.

Authors:  Liming Wang; Herman S Overkleeft; Gijsbert A van der Marel; Jeroen D C Codée
Journal:  J Am Chem Soc       Date:  2018-03-23       Impact factor: 15.419
  3 in total

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