Edwards, Alison A. and Fleet, George W.J. and Mayes, Benjamin A. and Hunter, Stuart J. and Tranter, George E. (2004) Circular dichroism studies of carbopeptoid-cyclodextrins. Chirality, 17 (S1). S114-S119. ISSN 0899-0042 .
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A series of sugar amino acids, based on open chain sugars, have been oligomerised and cyclised. The resulting cyclic carbopeptoids have been examined for desirable properties such as host–guest chemistry (as in cyclodextrins) or self-assembling properties (e.g., peptide nanotubes). Initial studies of these systems, by circular dichroism and X-ray crystallography, have given valuable insight into their stability and properties. One of the four cyclic species studied was found to interact with ion/molecular probes.
Q Science > QD Chemistry
|Divisions:||Faculties > Science Technology and Medical Studies > Medway School of Pharmacy|
|Depositing User:||Alison Edwards|
|Date Deposited:||08 Sep 2008 14:58|
|Last Modified:||28 May 2012 10:46|
|Resource URI:||http://kar.kent.ac.uk/id/eprint/4887 (The current URI for this page, for reference purposes)|
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