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Novel octapeptide as an asymmetric catalyst for Michael reaction in aqueous media


Citation

Bayat, Saadi and Abd. Malek, Emilia and Tejo, Bimo Ario and Salleh, Abu Bakar and Mohd Yahaya, Normi and Abdul Rahman, Mohd Basyaruddin (2013) Novel octapeptide as an asymmetric catalyst for Michael reaction in aqueous media. Synthetic Communications, 43 (23). pp. 3130-3140. ISSN 0039-7911; ESSN: 1532-2432

Abstract

In this work, three forms of a novel octapeptide have been evaluated as asymmetric catalysts for the Michael reaction. Low quantity catalyst loading, ecofriendly solvents, and reusability of organocatalyst successfully applied to attain excellent yields and moderate enantioselectivities in the Michael reaction.


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Additional Metadata

Item Type: Article
Divisions: Faculty of Biotechnology and Biomolecular Sciences
Faculty of Science
DOI Number: https://doi.org/10.1080/00397911.2012.762686
Publisher: Taylor & Francis
Keywords: Asymmetric; Enantioselectivities; Michael reaction; Octapeptide; Organocatalyst; Reusablity.
Depositing User: Umikalthom Abdullah
Date Deposited: 20 Oct 2014 07:47
Last Modified: 25 Aug 2015 01:17
Altmetrics: http://www.altmetric.com/details.php?domain=psasir.upm.edu.my&doi=10.1080/00397911.2012.762686
URI: http://psasir.upm.edu.my/id/eprint/30273
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