Chandrasekhar, Sosale and Karri, Phaneendrasai (2007) Erlenmeyer azlactone synthesis with aliphatic aldehydes under solvent-free microwave conditions. In: Tetrahedron Letters, 48 (5). pp. 785-786.
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Abstract
2-Phenyl-5(4H)-oxazolone (azlactone) reacts with aliphatic aldehydes upon adsorption on neutral alumina and irradiation with microwaves (<2 min). The corresponding condensation products are obtained in good yields (62–78%), indicating the satisfactory resolution of a long-standing problem plaguing the classical Erlenmeyer synthesis (poor results with aliphatic aldehydes). Plausible mechanistic reasons for the success of the procedure are discussed.
Item Type: | Journal Article |
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Publication: | Tetrahedron Letters |
Publisher: | Elsevier |
Additional Information: | Copyright of this article belongs to Elsevier. |
Department/Centre: | Division of Chemical Sciences > Organic Chemistry |
Date Deposited: | 27 Mar 2007 |
Last Modified: | 19 Sep 2010 04:36 |
URI: | http://eprints.iisc.ac.in/id/eprint/10234 |
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