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dc.contributor.authorKondoh, Azusa
dc.contributor.authorJamison, Timothy F.
dc.date.accessioned2013-11-15T17:00:47Z
dc.date.available2013-11-15T17:00:47Z
dc.date.issued2010-01
dc.date.submitted2009-10
dc.identifier.issn1359-7345
dc.identifier.issn1364-548X
dc.identifier.urihttp://hdl.handle.net/1721.1/82127
dc.description.abstractA rhodium-catalyzed dehydrogenative borylation of cyclic alkenes is described. This reaction provides direct access to cyclic 1-alkenylboronic acid pinacol esters, useful intermediates in organic synthesis. Suzuki–Miyaura cross-coupling applications are also presented.en_US
dc.description.sponsorshipNational Institute of General Medical Sciences (U.S.) (GM-63755)en_US
dc.language.isoen_US
dc.publisherRoyal Society of Chemistryen_US
dc.relation.isversionofhttp://dx.doi.org/10.1039/b921387ben_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alike 3.0en_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/en_US
dc.sourcePMCen_US
dc.titleRhodium-catalyzed dehydrogenative borylation of cyclic alkenesen_US
dc.typeArticleen_US
dc.identifier.citationKondoh, Azusa, and Timothy F. Jamison. “Rhodium-catalyzed dehydrogenative borylation of cyclic alkenes.” Chemical Communications 46, no. 6 (2010): 907.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.mitauthorKondoh, Azusaen_US
dc.contributor.mitauthorJamison, Timothy F.en_US
dc.relation.journalChemical Communicationsen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsKondoh, Azusa; Jamison, Timothy F.en_US
dc.identifier.orcidhttps://orcid.org/0000-0002-8601-7799
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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