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J Am Chem Soc ; 132(39): 13666-8, 2010 Oct 06.
Article in English | MEDLINE | ID: mdl-20822182

ABSTRACT

Direct C-4-selective addition of pyridine across alkenes and alkynes is achieved for the first time by nickel/Lewis acid cooperative catalysis with an N-heterocyclic carbene ligand. A variety of substituents on both alkenes and pyridine are tolerated to give linear 4-alkylpyridines in modest to good yields. The addition across styrene, on the other hand, gives branched 4-alkylpyridines. A single example of C-4-selective alkenylation is also described.


Subject(s)
Acids/chemistry , Nickel/chemistry , Organometallic Compounds/chemistry , Pyridines/chemical synthesis , Alkenes/chemistry , Alkylation , Alkynes/chemistry , Catalysis , Ligands , Molecular Structure , Pyridines/chemistry , Stereoisomerism
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