Photo??Cross??Coupling Reaction of Electron??Rich Aryl Chlorides and Aryl Esters with Alkynes: A Metal??Free Alkynylation
S Protti, M Fagnoni, A Albini
Index: De Carolis, Marco; Protti, Stefano; Fagnoni, Maurizio; Albini, Angelo Angewandte Chemie - International Edition, 2005 , vol. 44, # 8 p. 1232 - 1236
Full Text: HTML
Citation Number: 68
Abstract
Aryl acetylenes are versatile intermediates in organic synthesis in view of the easy derivatization of their triple bonds [1] and find application in molecular electronics.[2] The elective method for the synthesis of these compounds is the Sonogashira reaction, which involves the Pd/Cu-mediated formation of a C (sp2) ÀC (sp) bond. Despite many efforts to improve this method, the most popular protocol in use today still consists of a mixture of an ...
Related Articles:
[Littke, Adam F.; Schwarz, Lothar; Fu, Gregory C. Journal of the American Chemical Society, 2002 , vol. 124, # 22 p. 6343 - 6348]
[Mayer, Matthias; Czaplik, Waldemar M.; Von Wangelin, Axel Jacobi Advanced Synthesis and Catalysis, 2010 , vol. 352, # 13 p. 2147 - 2152]
[Denmark, Scott E.; Werner, Nathan S. Journal of the American Chemical Society, 2008 , vol. 130, # 48 p. 16382 - 16393]
[Organic Letters, , vol. 5, # 7 p. 1043 - 1045]
[Carrera, Nora; Salinas-Castillo, Alfonso; Albeniz, Ana C.; Espinet, Pablo; Mallavia, Ricardo Journal of Organometallic Chemistry, 2011 , vol. 696, # 21 p. 3316 - 3321]