Document Detail


Cyclic oligomers of oxetane-based dipeptide isosteres derived from L-rhamnose.
MedLine Citation:
PMID:  16710869     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Two new cyclic oligomers, cyclo-tetra-[2,4-anhydro-3-O-tert-butyldimethylsilyl-5-deoxy-L-rhamnonamido-(N-->5)] and the corresponding 6-deoxy-D-gulonate cyclic "tetramer", have been synthesised from linear tetrameric oligomers, using TBTU- and pentafluorophenyl ester-based methodologies, respectively. These two compounds constitute a novel class of cyclic oligomers derived from oxetane-based sugar amino acids.
Authors:
George W J Fleet; Stephen W Johnson; John H Jones
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Journal of peptide science : an official publication of the European Peptide Society     Volume:  12     ISSN:  1075-2617     ISO Abbreviation:  J. Pept. Sci.     Publication Date:  2006 Aug 
Date Detail:
Created Date:  2006-08-22     Completed Date:  2006-09-25     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9506309     Medline TA:  J Pept Sci     Country:  England    
Other Details:
Languages:  eng     Pagination:  559-61     Citation Subset:  IM    
Copyright Information:
Copyright (c) 2006 European Peptide Society and John Wiley & Sons, Ltd.
Affiliation:
Chemistry Research Laboratory, Department of Chemistry, University of Oxford, Mansfield Road, Oxford OX1 3TA, UK.
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MeSH Terms
Descriptor/Qualifier:
Dipeptides / chemical synthesis*,  chemistry
Ethers, Cyclic / chemistry*
Indicators and Reagents
Molecular Structure
Rhamnose / chemistry*
Stereoisomerism
Chemical
Reg. No./Substance:
0/Dipeptides; 0/Ethers, Cyclic; 0/Indicators and Reagents; 10485-94-6/Rhamnose; 503-30-0/oxetane

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