Raj, Monika ; Veerasamy, Nagarathanam ; Singh, Vinod K. (2010) Highly enantioselective synthesis of 3-cycloalkanone-3-hydroxy-2-oxindoles, potential anticonvulsants Tetrahedron Letters, 51 (16). pp. 2157-2159. ISSN 0040-4039
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Official URL: http://www.sciencedirect.com/science/article/pii/S...
Related URL: http://dx.doi.org/10.1016/j.tetlet.2010.02.082
Abstract
Highly enantioselective catalytic synthesis of 3-cycloalkanone-3-hydroxy-2-oxindoles was achieved by using primary-tertiary diamine-Brønsted acid catalyst in both organic medium and aqueous medium. The products, thus obtained act as potential anticonvulsants.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| Keywords: | Aldol Reaction; Aqueous Medium; Organocatalyst; Enantioselective Reaction; Anticonvulsants |
| ID Code: | 55450 |
| Deposited On: | 18 Aug 2011 08:49 |
| Last Modified: | 18 Aug 2011 08:49 |
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