New N-Heterocyclic Carbene Palladium Complex/Ionic Liquid Matrix Immobilized on Silica: Application as Recoverable Catalyst for the Heck Reaction; B. Karimi, D. Enders, Org. Lett., 2006, 8, 1237-1240.
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www.organic-chemistry.org/namedreactions/heck-reaction....
www.organic-chemistry.org/namedreactions/heck-reaction.shtm
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Computational study of a new Heck reaction mechanism catalyzed by palladium(II/IV) species Andreas Sundermann, Olivier Uzan, and Jan M.L. Martin* Heck (0-II) pathway:
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theochem.weizmann.ac.il/web/papers/heck.html
theochem.weizmann.ac.il/web/papers/heck.html
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Myers The Heck Reaction Chem 115; R' R; R'; Reviews: Brase, S.; de Meijere, A. In Metal-catalyzed Cross-coupling Reactions, Diederich, F., and Stang, P. J., Link, J. T.; Overman, L. E. In Metal-catalyzed Cross-coupling Reactions, Diederich, F., and;
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www.chem.harvard.edu/groups/myers/handouts/Heck.pdf
www.chem.harvard.edu/groups/myers/handouts/Heck.pdf
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Return to Named Reactions If you would like to contribute a current example, please send it to...
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orgchem.chem.uconn.edu/namereact/heckre.html
orgchem.chem.uconn.edu/namereact/heckre.html
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The Mizoroki-Heck reaction is a palladium-catalyzed carbon–carbon bond forming process which is widely used in organic and organometallic synthesis.
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www.wiley.com/WileyCDA/WileyTitle/productCd-0470033940....
www.wiley.com/WileyCDA/WileyTitle/productCd-0470033940.html
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Richard F. Heck is an American chemist best known for the Heck reaction, the Pd-mediated coupling of an aryl halide with an alkene, the reaction that has...
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www.absoluteastronomy.com/topics/Heck_reaction
www.absoluteastronomy.com/topics/Heck_reaction
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The second in a series of two papers, this study examines the origins of diastereoselection in the second ring closure of the highly diastereoselective double Heck cyclization of cyclohexenes 1 and 3 that form contiguous quaternary stereocenters. The Asymmetric Intramolecular Heck Reaction in Natural Product Total Synthesis...
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pubs.acs.org/cgi-bin/abstract.cgi/joceah/2006/71/i07/ab...
pubs.acs.org/cgi-bin/abstract.cgi/joceah/2006/71/i07/abs/jo0523363.html
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Diastereoselective double Heck cyclizations of cyclohexene diamides 1 and 3 form contiguous quaternary stereocenters, with diastereoselection being controlled by the trans-diol protecting group. Diastereoselection in the Formation of Contiguous Quaternary Carbon Stereocenters by the Intramolecular Heck Reaction...
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pubs.acs.org/doi/abs/10.1021/jo052335a
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Heck reactions use palladium acetate as the preferred precatalyst to effect vinylic substitutions involving haloarenes and haloalkenes. The microscale synthesis described uses a reaction between a bromoiodobenzene and acrylic acid to produce a bromocinnamic acid.
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www.jce.divched.org/Journal/Issues/2000/Jun/abs757.html
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