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|Title:||Synthesis and intramolecular inclusion of β-cyclodextrins linked with a cyclohexyl group||Authors:||Li, D.B.
|Issue Date:||4-Mar-2002||Citation:||Li, D.B., Ng, S.-C., Novak, I. (2002-03-04). Synthesis and intramolecular inclusion of β-cyclodextrins linked with a cyclohexyl group. Tetrahedron Letters 43 (10) : 1871-1875. ScholarBank@NUS Repository. https://doi.org/10.1016/S0040-4039(02)00019-9||Abstract:||Cyclohexanecarboxylic acid (6A-deoxy-β-cyclodextrin-6A-C-yl)-amide (CHC-βCD) was synthesized via an aza-Wittig reaction and found to form in water, a temperature-independent intramolecular complex with its own cyclohexyl moiety. The analysis was based on data from 2D and variable-temperature NMR spectroscopy. The self-inclusion behavior of peracetylated CHC-βCD (PACHC-βCD) in chloroform was also investigated. © 2002 Elsevier Science Ltd. All rights reserved.||Source Title:||Tetrahedron Letters||URI:||http://scholarbank.nus.edu.sg/handle/10635/95069||ISSN:||00404039||DOI:||10.1016/S0040-4039(02)00019-9|
|Appears in Collections:||Staff Publications|
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