Literature DB >> 21735005

New insight on 2-naphthylmethyl (NAP) ether as a protecting group in carbohydrate synthesis: a divergent approach towards a high-mannose type oligosaccharide library.

Yao Li1, Bimalendu Roy, Xinyu Liu.   

Abstract

A new method for selective cleavage of 2-naphthylmethyl (NAP) ether utilizing 10-20 molar excess of HF/pyridine in toluene was revealed and strategically applied to a divergent approach towards generation of a high-mannose type oligosaccharide library. This journal is © The Royal Society of Chemistry 2011

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Year:  2011        PMID： 21735005     DOI： 10.1039/c1cc13264d

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN： 1359-7345            Impact factor:   6.222


  4 in total

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Authors:  Sanyong Zhu; Zhongwu Guo
Journal:  Org Lett       Date:  2017-05-25       Impact factor: 6.005

2.  Hydrogenolytic cleavage of naphthylmethyl ethers in the presence of sulfides.

Authors:  Philip O Adero; Dean R Jarois; David Crich
Journal:  Carbohydr Res       Date:  2017-06-20       Impact factor: 2.104

3.  Serratamolide is a hemolytic factor produced by Serratia marcescens.

Authors:  Robert M Q Shanks; Nicholas A Stella; Roni M Lahr; Shaoru Wang; Tara I Veverka; Regis P Kowalski; Xinyu Liu
Journal:  PLoS One       Date:  2012-05-16       Impact factor: 3.240

4.  Mild Method for 2-Naphthylmethyl Ether Protecting Group Removal Using a Combination of 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) and β-Pinene.

Authors:  Dina Lloyd; Marissa Bylsma; Danielle K Bright; Xizhao Chen; Clay S Bennett
Journal:  J Org Chem       Date:  2017-03-27       Impact factor: 4.354
  4 in total

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