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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/3292
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dc.contributor.authorShukla, Paritosh-
dc.date.accessioned2021-11-11T10:54:07Z-
dc.date.available2021-11-11T10:54:07Z-
dc.date.issued2006-
dc.identifier.urihttps://www.organic-chemistry.org/abstracts/lit1/106.shtm-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3292-
dc.description.abstractAn efficient cobalt-catalyzed reductive coupling reaction of alkyl halides with alkenes bearing electron-withdrawing groups in the presence of water and zinc powder in acetonitrile gave the corresponding Michael-type addition products in high yields. The mechanism is discussed.en_US
dc.language.isoenen_US
dc.publisherOCPen_US
dc.subjectChemistryen_US
dc.subjectCobalt-Catalyzeden_US
dc.subjectAlkyl Halidesen_US
dc.titleCobalt-Catalyzed Reductive Coupling of Saturated Alkyl Halides with Activated Alkenes Paritosh Shukla, Yun-Chu Hsu and Chien-Hong Chengen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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