Literature DB >> 16529729

NMR evidence for the participation of triflated ionic liquids in glycosylation reaction mechanisms.

Anna Rencurosi1, Luigi Lay, Giovanni Russo, Enrico Caneva, Laura Poletti.   

Abstract

A systematic low-temperature NMR study of a glycosylation reaction was performed in the presence of different ionic liquids and acidic catalysts. The influence of the triflate anion derived from [emim][OTf] on the stereochemistry of the glycosylation products was evaluated.

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Year:  2006        PMID： 16529729     DOI： 10.1016/j.carres.2006.02.021

Source DB:  PubMed          Journal:  Carbohydr Res        ISSN： 0008-6215            Impact factor:   2.104


  6 in total

1.  Glycosylation in room temperature ionic liquid using unprotected and unactivated donors.

Authors:  Tae-Joon Park; Michel Weïwer; Xuejun Yuan; Sultan N Baytas; Eva M Munoz; Saravanababu Murugesan; Robert J Linhardt
Journal:  Carbohydr Res       Date:  2006-11-29       Impact factor: 2.104

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Journal:  J Org Chem       Date:  2017-09-05       Impact factor: 4.354

3.  Methodology development and physical organic chemistry: a powerful combination for the advancement of glycochemistry.

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Journal:  J Org Chem       Date:  2011-10-04       Impact factor: 4.354

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Authors:  James T Smoot; Alexei V Demchenko
Journal:  J Org Chem       Date:  2008-10-22       Impact factor: 4.354

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

Authors:  Swati S Nigudkar; Alexei V Demchenko
Journal:  Chem Sci       Date:  2015-05-01       Impact factor: 9.825

6.  Self-promoted and stereospecific formation of N-glycosides.

Authors:  Michael Martin Nielsen; Patrycja Mała; Eirikur Þórir Baldursson; Christian Marcus Pedersen
Journal:  Chem Sci       Date:  2019-04-18       Impact factor: 9.825
  6 in total

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