1) Tetrahedron, Vol. 61, Is. 41, 2005, P. 9908-9917
A practical synthesis of highly functionalized aryl nitriles through cyanation of aryl bromides employing heterogeneous Pd/C: in quest of an industrially viable process
Masanori Hatsudaa and Masahiko Sekib.
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http://dx.doi.org/10.1016/j.tet.2005.06.061Improving palladium-catalyzed cyanation of aryl halides: development of a state-of-the-art methodology using potassium hexacyanoferrate(II) as cyanating agent
Thomas Schareina, Alexander Zapf and Matthias Beller,
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http://dx.doi.org/10.1016/j.jorganchem.2004.083)Tetrahedron Letters, V. 47, Is. 19, 2006, P. 3303-3305
A facile microwave-assisted palladium-catalyzed cyanation of aryl chlorides
Harry R. Chobanian, , Brett P. Fors and Linus S. Lin
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http://dx.doi.org/10.1016/j.tetlet.2006.03.026An environmentally benign procedure for the Cu-catalyzed cyanation of aryl bromides
Thomas Schareina, Alexander Zapf and Matthias Beller,
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http://dx.doi.org/10.1016/j.tetlet.2005.02.106 Statistical experimental design-driven discovery of room-temperature conditions for palladium-catalyzed cyanation of aryl bromides
Federica Stazia, Giovanni Palmisanoa, Marco Turconib and Marco Santagostinob
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http://dx.doi.org/10.1016/j.tetlet.2005.01.116A practical synthesis of highly functionalized aryl nitriles through cyanation of aryl bromides employing heterogeneous Pd/C
Masanori Hatsudaa and Masahiko Sekib.
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http://dx.doi.org/10.1016/j.tetlet.2005.01.098Application of polymer-supported triphenyl phosphine in the palladium-catalyzed cyanation reaction under microwave conditions
Rajiv R. Srivastava, and Scott E. Collibee
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http://dx.doi.org/10.1016/j.tetlet.2004.09.184