An efficient and safe procedure for the large-scale Pd-catalyzed hydrazonation of aromatic chlorides using buchwald technology
CC Mauger, GA Mignani
Index: Mauger, Christelle C.; Mignani, Gerard A. Organic Process Research and Development, 2004 , vol. 8, # 6 p. 1065 - 1071
Full Text: HTML
Citation Number: 32
Abstract
A convenient, optimized and safe synthesis of N-arylhydrazines, useful as intermediates for active ingredients in agricultural and pharmaceutical applications, is reported. Starting from aryl halides (chlorides and bromides), a palladium-catalyzed carbon-nitrogen coupling reaction followed by an acidic treatment afforded the target molecules in good to excellent yields using low catalyst loadings. This technology has then been successfully applied on ...
Related Articles:
Highly active palladium catalysts for Suzuki coupling reactions
[Wolfe, John P.; Singer, Robert A.; Yang, Bryant H.; Buchwald, Stephen L. Journal of the American Chemical Society, 1999 , vol. 121, # 41 p. 9550 - 9561]
[Kaye, Steven; Fox, Joseph M.; Hicks, Frederick A.; Buchwald, Stephen L. Advanced Synthesis and Catalysis, 2001 , vol. 343, # 8 p. 789 - 794]
[Ullah, Ehsan; McNulty, James; Robertson, Al European Journal of Organic Chemistry, 2012 , # 11 p. 2127 - 2131]
Highly active palladium catalysts for Suzuki coupling reactions
[Journal of the American Chemical Society, , vol. 121, # 41 p. 9550 - 9561]
Highly active palladium catalysts for Suzuki coupling reactions
[Journal of the American Chemical Society, , vol. 121, # 41 p. 9550 - 9561]