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dc.contributor.authorShukla, Paritosh-
dc.date.accessioned2021-11-11T10:54:12Z-
dc.date.available2021-11-11T10:54:12Z-
dc.date.issued2003-
dc.identifier.urihttps://pubs.acs.org/doi/10.1021/ol036027f-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3293-
dc.description.abstractIn 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.isoenen_US
dc.publisherACSen_US
dc.subjectChemistryen_US
dc.subjectHydrocarbonsen_US
dc.subjectAromatic compoundsen_US
dc.subjectAmidesen_US
dc.titleCyclization of Oxa-Bicyclic Alkenes with β-Iodo-(Z)-propenoates and o-Iodobenzoate Catalyzed by Nickel Complexes:  A Simple Efficient Route to Annulated Coumarinsen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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