View Item 

Show simple item record

Activation of Pyridinium Salts for Electrophilic Acylation: a Method for Conversion of Pyridines into 3-Acylpyridines
dc.contributor.authorKlapars, A.en_US
dc.contributor.authorVedejs, Edwinen_US
dc.date.accessioned2006-09-08T19:20:40Z
dc.date.available2006-09-08T19:20:40Z
dc.date.issued2004-06en_US
dc.identifier.citationKlapars, A.; Vedejs, E.; (2004). "Activation of Pyridinium Salts for Electrophilic Acylation: a Method for Conversion of Pyridines into 3-Acylpyridines." Chemistry of Heterocyclic Compounds 40(6): 759-766. <http://hdl.handle.net/2027.42/41517>en_US
dc.identifier.issn0009-3122en_US
dc.identifier.issn1573-8353en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/41517
dc.description.abstractCyanide adducts of N-MOM pyridinium salts react with strong acylating reagents to provide 3-acyl-4-cyano-1,4-dihydropyridines that can be aromatized to 3-acylpyridines using ZnCl 2 in refluxing ethanol.en_US
dc.format.extent212891 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherKluwer Academic Publishers-Plenum Publishers; Plenum Publishing Corporation ; Springer Science+Business Mediaen_US
dc.subject.otherChemistryen_US
dc.subject.otherOrganic Chemistryen_US
dc.subject.otherDihydropyridinesen_US
dc.subject.otherPyridine Acylationen_US
dc.titleActivation of Pyridinium Salts for Electrophilic Acylation: a Method for Conversion of Pyridines into 3-Acylpyridinesen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbsecondlevelMaterials Science and Engineeringen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, MI 48109, USAen_US
dc.contributor.affiliationotherDepartment of Process Research, Merck Research Laboratories, NJ 07065, USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/41517/1/10593_2004_Article_496956.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1023/B:COHC.0000040772.13427.0ben_US
dc.identifier.sourceChemistry of Heterocyclic Compoundsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


Files in this item

Name:
10593_2004_Article_496956.pdf
Size:
207.9KB
Format:
PDF
View/Open

Show simple item record

Remediation of Harmful Language

The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.

Accessibility

If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.