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Cyclization of Oxa-Bicyclic Alkenes with β-Iodo-(Z)-propenoates and o-Iodobenzoate Catalyzed by Nickel Complexes:  A Simple Efficient Route to Annulated Coumarins

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dc.contributor.author Shukla, Paritosh
dc.date.accessioned 2021-11-11T10:54:12Z
dc.date.available 2021-11-11T10:54:12Z
dc.date.issued 2003
dc.identifier.uri https://pubs.acs.org/doi/10.1021/ol036027f
dc.identifier.uri http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3293
dc.description.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. en_US
dc.language.iso en en_US
dc.publisher ACS en_US
dc.subject Chemistry en_US
dc.subject Hydrocarbons en_US
dc.subject Aromatic compounds en_US
dc.subject Amides en_US
dc.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 en_US
dc.type Article en_US


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