Pd-catalyzed carbonylative reactions of aryl iodides and alkynyl carboxylic acids via decarboxylative couplings
A Park, K Park, Y Kim, S Lee
Index: Park, Ahbyeol; Park, Kyungho; Kim, Yong; Lee, Sunwoo Organic Letters, 2011 , vol. 13, # 5 p. 944 - 947
Full Text: HTML
Citation Number: 53
Abstract
Alkynyl carboxylic acids reacted with aryl iodides under a CO atmosphere in the presence of a palladium catalyst to produce α, β-alkynyl aryl ketones in good yields. The maximum turnover number was 16 800. The desired carbonylative coupling was formed from phenyl propiolic acid without any formation of a noncarbonylative coupling product in the absence of CuI. However, the reaction with alkyl-substituted alkynyl carboxylic acids required CuI ...
Related Articles:
[Weerasiri, Kushan C.; Gorden, Anne E. V. European Journal of Organic Chemistry, 2013 , # 8 p. 1546 - 1550]
[Morales-Serna, Jose Antonio; Sauza, Alejandro; Padron De Jesus, Gabriela; Gavino, Ruben; Garcia De La Mora, Gustavo; Cardenas, Jorge Tetrahedron Letters, 2013 , vol. 54, # 52 p. 7111 - 7114]
[Mohammadi, Elmira; Movassagh, Barahman; Navidi, Mozhgan Helvetica Chimica Acta, 2014 , vol. 97, # 1 p. 70 - 75]
Palladium-catalyzed Sonogashira cross-coupling of organic tellurides with alkynes
[Kawaguchi, Shin-Ichi; Srivastava, Puneet; Engman, Lars Tetrahedron Letters, 2011 , vol. 52, # 32 p. 4120 - 4122]
Si-Based Benzylic 1, 4-Rearrangement/Cyclization Reaction
[Trost, Barry M.; Bertogg, Andreas Organic Letters, 2009 , vol. 11, # 3 p. 511 - 513]