67330-35-2Relevant academic research and scientific papers
An efficient general method for esterification of aromatic carboxylic acids
Hosangadi, Bhaskar D.,Dave, Rajesh H.
, p. 6375 - 6378 (1996)
Treatment of a variety of aromatic carboxylic acids with alcohols in the presence of thionyl chloride results in excellent yields of corresponding esters. This esterification system is compatible with a wide assortment of functional groups.
Efficient copper-catalyzed Sonogashira coupling reactions and simulation studies
Ali, Imran,Nighot, Dnyaneshwar,Lone, Mohammad Nadeem,Jain, Arvind
supporting information, p. 1175 - 1184 (2017/06/09)
A practical copper-catalyzed I-substitutions of alkyl-2-iodobenzoates with alkynes have been developed using Cu powder as a catalyst under solvent, cocatalyst, and base-free conditions. This reaction system is new, facile, efficient, and economical that g
2-Iodoxybenzoic acid-mediated transformation of halogenated hydrocarbon in the presence of tetraethyl ammonium bromide
Zhang, Yuan,Han, Jianlei,Xu, Yanjun,Wei, Yuping
experimental part, p. 303 - 307 (2012/09/25)
2-Iodoxybenzoic acid (IBX) has been shown to react with alkyl halides in the presence of tetraethyl ammonium bromide to give 2-iodobenzoate esters. Most of the monohalides and dihalides reacted easily with moderate to good yields. The 2-iodobenzoate ester
Gold-catalyzed C-S bond formation from thiols
Jean, Micka?l,Renault, Jacques,van de Weghe, Pierre,Asao, Naoki
supporting information; experimental part, p. 378 - 381 (2010/03/24)
ortho-Alkynylbenzoic acid alkyl esters act as alkylating agents of thiol derivatives with PPh3AuCl in combination with AgOTf in 1,2-dichloroethane at 80 °C. The corresponding sulfide compounds are obtained in good to excellent yields.
