Document Detail


In situ formation of β-glycosyl imidinium triflate from participating thioglycosyl donors: elaboration to disarmed-armed iterative glycosylation.
MedLine Citation:
PMID:  23023321     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
β-Glycosyl imidinium triflate is generated from participating thioglycoside donors for disarmed-armed iterative glycosylations and one-pot oligosaccharide synthesis.
Authors:
Yu Hsien Lin; Bhaswati Ghosh; Kwok-Kong Tony Mong
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Chemical communications (Cambridge, England)     Volume:  48     ISSN:  1364-548X     ISO Abbreviation:  Chem. Commun. (Camb.)     Publication Date:  2012 Nov 
Date Detail:
Created Date:  2012-10-11     Completed Date:  2013-03-26     Revised Date:  2014-01-31    
Medline Journal Info:
Nlm Unique ID:  9610838     Medline TA:  Chem Commun (Camb)     Country:  England    
Other Details:
Languages:  eng     Pagination:  10910-2     Citation Subset:  IM    
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MeSH Terms
Descriptor/Qualifier:
Glycosylation
Magnetic Resonance Spectroscopy
Mesylates / chemical synthesis*
Molecular Structure
Thioglycosides / chemistry*
Chemical
Reg. No./Substance:
0/Mesylates; 0/Thioglycosides; JE2SY203E8/trifluoromethanesulfonic acid
Comments/Corrections
Erratum In:
Chem Commun (Camb). 2013 Dec 28;49(100):11819

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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