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

dc.contributor.authorShukla, Paritosh
dc.date.accessioned2021-11-11T10:54:12Z
dc.date.available2021-11-11T10:54:12Z
dc.date.issued2003
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.identifier.urihttps://pubs.acs.org/doi/10.1021/ol036027f
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3293
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

Files

License bundle

Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.71 KB
Format:
Item-specific license agreed upon to submission
Description: