- Title
- 1H NMR-based kinetic-mechanistic study of the intramolecular trans-esterification of 2-exo-3-exo-dihydroxybornane monoacrylate esters
- Creator
- Duggan, Andrew R
- Creator
- Mciteka, Lulama P
- Creator
- Lobb, Kevin A
- Creator
- Kaye, Perry T
- Subject
- To be catalogued
- Date Issued
- 2013
- Date
- 2013
- Type
- text
- Type
- article
- Identifier
- http://hdl.handle.net/10962/448871
- Identifier
- vital:74767
- Identifier
- xlink:href="https://hdl.handle.net/10520/EJC135616"
- Description
- A 1H NMR study of the acid-catalyzed, intramolecular trans-esterification between isomeric 2-exo-3-exo-dihydroxybornane monoacrylate esters has afforded insights into the reaction mechanism and permitted the determination of kinetic and thermodynamic parameters for the pseudo-first-order processes.
- Format
- computer
- Format
- online resource
- Format
- application/pdf
- Format
- 1 online resource (5 pages)
- Format
- Publisher
- Sabinet
- Language
- English
- Relation
- South African Journal of Chemistry
- Relation
- Duggan, A.R., Mciteka, L.P., Lobb, K.A. and Kaye, P.T., 2013. 1H NMR-based kinetic-mechanistic study of the intramolecular trans-esterification of 2-exo-3-exo-dihydroxybornane monoacrylate esters. South African Journal of Chemistry, 66(1), pp.140-144
- Relation
- South African Journal of Chemistry volume 66 number 1 p. 140 2013 1532-2432
- Rights
- Publisher
- Rights
- Use of this resource is governed by the terms and conditions of the Sabinet Terms and Conditions Statement (https://www.sabinet.co.za/terms-conditions)
- Rights
- Open Access
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