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. Copyright © 2006 European Peptide Society and John Wiley and Sons, Ltd.

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APA Style

Fleet, G., Johnson, S., & Jones, J. (2006). Cyclic oligomers of oxetane-based dipeptide isosteres derived from L-rhamnose. Journal of Peptide Science, 12(8), 559–561.

MLA Style

Fleet, G., et al. “Cyclic Oligomers of Oxetane-Based Dipeptide Isosteres Derived from L-Rhamnose.” Journal of Peptide Science, vol. 12, no. 8, 2006, pp. 559–61.

Chicago Style

Fleet, G, S Johnson, and J Jones. 2006. “Cyclic Oligomers of Oxetane-Based Dipeptide Isosteres Derived from L-Rhamnose.” Journal of Peptide Science 12 (8): 559–61.
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Publisher copy:: 10.1002/psc.759

Authors

+ Fleet, G More by this author

Institution:: University of Oxford
Division:: MPLS
Department:: Chemistry
Sub department:: Organic Chemistry
Role:: Author

+ Johnson, S More by this author

Role:: Author

+ Jones, J More by this author

Role:: Author

Journal:: Journal of Peptide Science More from this journal
Volume:: 12
Issue:: 8
Pages:: 559-561
Publication date:: 2006-08-01
DOI:: 10.1002/psc.759
EISSN:: 1099-1387
ISSN:: 1075-2617

Language:: English
Keywords:: Oxetane

Rhamnose

Cyclopeptidomimetics

Cyclic oligomers

Dipeptide isostere
Pubs id:: pubs:160248
UUID:: uuid:f46b8f29-6df3-41ed-bc6e-f874ce5a1fa9
Local pid:: pubs:160248
Source identifiers:: 160248
Deposit date:: 2012-12-19

Terms of use

Copyright date:: 2006

Licence:: Terms and Conditions of Use for Oxford University Research Archive

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