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Journal article

Cyclic oligomers of oxetane-based dipeptide isosteres derived from L-rhamnose.

Abstract:
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.
Publication status:
Published

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Publisher copy:
10.1002/psc.759

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Journal:
Journal of peptide science : an official publication of the European Peptide Society
Volume:
12
Issue:
8
Pages:
559-561
Publication date:
2006-08-05
DOI:
EISSN:
1099-1387
ISSN:
1075-2617
URN:
uuid:93d31e95-7608-475b-8e1f-99f263c69bc8
Source identifiers:
40098
Local pid:
pubs:40098

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