Palladium-Catalyzed Decarboxylative Cross-Coupling Reactions: A Route for Regioselective Functionalization of Coumarins

F Jafarpour, S Zarei…

Index: Bardajee, Ghasem Rezanejade; Jafarpour, Farnaz; Afsari, Hamid Samareh Central European Journal of Chemistry, 2010 , vol. 8, # 2 p. 370 - 374

Full Text: HTML

Citation Number: 25

Abstract

A straightforward, regioselective, and step-economical ligand-free palladium-catalyzed decarboxylative functionalization of coumarin-3-carboxylic acids is devised. This protocol is compatible with a wide variety of electron-donating and-withdrawing substituents and allows

Related Articles:

Design, synthesis, physicochemical properties, and evaluation of novel iron chelators with fluorescent sensors

[Journal of Medicinal Chemistry, , vol. 47, # 25 p. 6349 - 6362]

Synthesis of new fluorophores derived from monoazacrown ethers and coumarin nucleus

[Canadian Journal of Chemistry, , vol. 80, # 2 p. 169 - 174]

Synthesis and pharmacological evaluation of carboxycoumarins as a new antitumor treatment targeting lactate transport in cancer cells

[Bioorganic and Medicinal Chemistry, , vol. 21, # 22 p. 7107 - 7117]

LSER in the reaction between p-nitrobenzyl bromide and 2-mercaptobenzoxazole

[Journal of Chemical Research - Part S, , # 6 p. 354 - 355]

Design, synthesis, physicochemical properties, and evaluation of novel iron chelators with fluorescent sensors

[Ma, Yongmin; Luo, Wei; Quinn, Peter J.; Liu, Zudong; Hider, Robert C. Journal of Medicinal Chemistry, 2004 , vol. 47, # 25 p. 6349 - 6362]

More Articles...