Srikrishna, A and Venkateswarlu, S and Danieldoss, S and Sattigeri, JA (1995) Radical Cyclization Methodology to Lignans: Synthesis of (.+-.)- Enterolactone. In: Indian Journal of Chemistry - Section B: Organic and Medicinal Chemistry, 34 (8). pp. 679-681.
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Official URL: http://onlinelibrary.wiley.com/doi/10.1002/chin.19...
Abstract
Synthesis of enterolactone, the first lignan of human origin, starting from 3-methoxycinnamyl alcohol employing a 5-exo-trig radical cyclisation reaction of mixed bromoacetal as the key step is described.
| Item Type: | Editorials/Short Communications |
|---|---|
| Publication: | Indian Journal of Chemistry - Section B: Organic and Medicinal Chemistry |
| Publisher: | National Institute of Science Communication and Information Resources |
| Additional Information: | Copyright of this article belongs to National Institute of Science Communication and Information Resources. |
| Keywords: | other bioactive products;ring closure reactions |
| Department/Centre: | Division of Chemical Sciences > Organic Chemistry |
| Date Deposited: | 24 May 2011 06:08 |
| Last Modified: | 24 May 2011 06:08 |
| URI: | http://eprints.iisc.ac.in/id/eprint/37868 |
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