Editing Heck reaction (section)

=== Amino-Heck reaction ===
In the '''amino-Heck reaction''' a [[nitrogen]] to [[carbon]] bond is formed. In one example,<ref>{{cite journal | title = Palladium(0)-catalyzed synthesis of pyridines from β-acetoxy-γ,δ-unsaturated ketone oximes |author1=Mitsuru Kitamura |author2=Daisuke Kudo |author3=Koichi Narasaka | journal = [[Arkivoc]] | pages = JC–1563E | year = 2005 | url = http://www.arkat-usa.org/ark/journal/2006/I03_Coxon/1563/1563.asp}}</ref> an [[oxime]] with a strongly electron withdrawing group reacts [[Intramolecular reaction|intramolecular]]ly with the end of a [[diene]] to form a [[pyridine]] compound. The [[catalyst]] is [[tetrakis(triphenylphosphine)palladium(0)]] and the base is [[triethylamine]]. 
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[[File:Heck amino.svg|center|400px|Amino-Heck reaction]]
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! Amino-Heck reaction
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