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ChemInform Abstract: Aerobic Pd‐Catalyzed sp 3 C—H Olefination: A Route to Both N‐Heterocyclic Scaffolds and Alkenes.
dc.contributor.authorStowers, Kara J.en_US
dc.contributor.authorFortner, Kevin C.en_US
dc.contributor.authorSanford, Melanie S.en_US
dc.date.accessioned2011-11-10T15:32:48Z
dc.date.available2012-11-02T18:56:38Zen_US
dc.date.issued2011-09-13en_US
dc.identifier.citationStowers, Kara J.; Fortner, Kevin C.; Sanford, Melanie S. (2011). "ChemInform Abstract: Aerobic Pd‐Catalyzed sp 3 C—H Olefination: A Route to Both N‐Heterocyclic Scaffolds and Alkenes.." ChemInform 42(37): no-no. <http://hdl.handle.net/2027.42/86881>en_US
dc.identifier.issn0931-7597en_US
dc.identifier.issn1522-2667en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/86881
dc.description.abstractThe Pd‐catalyzed olefination and cyclization of various 2‐alkylpyridines and α,β‐unsaturated alkenes utilizes air as the terminal oxidant and provides a conceptually novel entry to 6,5‐nitrogen heterocycles, which constitute the cores of numerous alkaloid natural products.en_US
dc.publisherWILEY‐VCH Verlagen_US
dc.subject.otherFused Pyridine Derivativesen_US
dc.subject.otherRing Closure Reactionsen_US
dc.subject.otherCatalysis, Phase‐Transfer Catalysisen_US
dc.subject.otherAlkaloidsen_US
dc.titleChemInform Abstract: Aerobic Pd‐Catalyzed sp 3 C—H Olefination: A Route to Both N‐Heterocyclic Scaffolds and Alkenes.en_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelOrganic Chemistryen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationotherDep. Chem., Univ. Mich., Ann Arbor, MI 48109, USAen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/86881/1/201137155_ftp.pdf
dc.identifier.doi10.1002/chin.201137155en_US
dc.identifier.sourceChemInformen_US
dc.identifier.citedreferenceKara J. Stowers, Kevin C. Fortner, Melanie S. Sanford, Aerobic Pd‐Catalyzed sp 3 C.lb.H Olefination: A Route to Both N‐Heterocyclic Scaffolds and Alkenes., J. Am. Chem. Soc., 2011, 133, 6541 – 6544. DOI: 10.1021/ja2015586;en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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