Use of Molecular Oxygen as a Reoxidant in the Synthesis of 2-Substituted Benzothiazoles via Palladium-Catalyzed CH Functionalization/Intramolecular CS Bond Formation
作者:Kiyofumi Inamoto、Chisa Hasegawa、Junpei Kawasaki、Kou Hiroya、Takayuki Doi
DOI:10.1002/adsc.201000604
日期:2010.10.4
Molecularoxygen (O2) was successfully employed as a reoxidant in cyclizations of thiobenzanilides 1a–s through a palladium-catalyzed CH functionalization/intramolecular CS bondformation process, leading to an efficient, green method for the synthesis of 2-arylbenzothiazoles 2a–s. Addition of cesium fluoride (CsF) greatly enhanced the reactions, which produced variously substituted 2-arylbenzothiazoles
A highly efficient procedure for the synthesis of symmetrical thioureas by means of simple condensation of primary amines and carbon disulfide in 1-butyl-3-methylimidazolium chloride [BMIM][Cl] as a cheap and commercially available ionic liquid is presented. This procedure works for aromatic and aliphatic primary amines and give high to excellent yields of symmetrical thioureas without need for any catalyst or tedious work-up.
Discussion
作者:Zhenyu Wang
DOI:10.1111/0022-1082.00366
日期:2001.8
Kharidia,S.P. et al., Journal of the Indian Chemical Society, 1962, vol. 39, p. 43 - 46
作者:Kharidia,S.P. et al.
DOI:——
日期:——
Trivedi,J.P. et al., Journal of the Indian Chemical Society, 1966, vol. 43, p. 265 - 268