ePrints@IIScePrints@IISc Home | About | Browse | Latest Additions | Advanced Search | Contact | Help

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.

Full text not available from this repository. (Request a copy)
Official URL: http://onlinelibrary.wiley.com/doi/10.1002/chin.19...


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
Depositing User: Ms V Mangala
Date Deposited: 24 May 2011 06:08
Last Modified: 24 May 2011 06:08
URI: http://eprints.iisc.ac.in/id/eprint/37868

Actions (login required)

View Item View Item