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Radical Cyclization Methodology to Lignans: Synthesis of (.+-.)- Enterolactone

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
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.ernet.in/id/eprint/37868

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