Palladium-catalyzed cross-coupling reactions of carboxylic anhydrides with organozinc reagents
D Wang, Z Zhang
Index: Wang, Donghui; Zhang, Zhaoguo Organic Letters, 2003 , vol. 5, # 24 p. 4645 - 4648
Full Text: HTML
Citation Number: 64
Abstract
Negishi-type cross-coupling reaction was effected by employing organozincs and anhydrides or mixed anhydrides that formed in situ from sodium salts of the corresponding acids and ethyl chloroformate under the catalysis of palladium (0). A general method for preparing symmetrical/unsymmetrical ketones was developed.
Related Articles:
Transition metal-mediated oxidations utilizing monomeric iodosyl-and iodylarene species
[Yusubov, Mekhman S.; Nemykin, Victor N.; Zhdankin, Viktor V. Tetrahedron, 2010 , vol. 66, # 31 p. 5745 - 5752]
Ion exchange catalysis in oxidation of organic compounds with KMnO4
[Shaabani, Ahmad; Teimouri, Fatemeh; Lee, Donald G. Synthetic Communications, 2003 , vol. 33, # 6 p. 1057 - 1065]
[Farhadi; Ansari Journal of the Iranian Chemical Society, 2011 , vol. 8, # 2 p. 470 - 476]
Hydration of alkynes by a PtCl4-CO catalyst
[Baidossi, Wael; Lahav, Michal; Blum, Jochanan Journal of Organic Chemistry, 1997 , vol. 62, # 3 p. 669 - 672]
Hydration of alkynes by a PtCl4-CO catalyst
[Baidossi, Wael; Lahav, Michal; Blum, Jochanan Journal of Organic Chemistry, 1997 , vol. 62, # 3 p. 669 - 672]