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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/3293
Title: Cyclization of Oxa-Bicyclic Alkenes with β-Iodo-(Z)-propenoates and o-Iodobenzoate Catalyzed by Nickel Complexes:  A Simple Efficient Route to Annulated Coumarins
Authors: Shukla, Paritosh
Keywords: Chemistry
Hydrocarbons
Aromatic compounds
Amides
Issue Date: 2003
Publisher: ACS
Abstract: In the presence of Ni(dppe)Br2 and Zn powder in acetonitrile at 80 °C, oxa-bicyclic olefins undergo cyclization with o-iodobenzoate and with β-iodo-(Z)-propenoates to give the benzocoumarin derivatives in moderate to good yields. This methodology offers a simple efficient way for the synthesis of structurally complicate coumarins in one pot.
URI: https://pubs.acs.org/doi/10.1021/ol036027f
http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3293
Appears in Collections:Department of Chemistry

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