1265154-47-9Relevant academic research and scientific papers
A highly efficient synthesis of 2,5-disubstituted furans from enyne acetates catalyzed by lewis acid and palladium
Chen, Zheng-Wang,Luo, Miao-Ting,Wen, Yue-Lu,Ye, Min,Zhou, Zhong-Gao,Liu, Liang-Xian
supporting information, p. 2341 - 2344 (2015/08/06)
A highly efficient synthesis of a wide range of 2,5-disubstituted furans from enyne acetates is described. The reactions are conducted by using Lewis acid and palladium catalyst and provide symmetrical and unsymmetrical products in good to excellent yields, with broad substrate scope, including a variety of aromatic and aliphatic substituents in the 2- and 5-position of the furan ring.
Synthesis of 2,5-disubstituted 3-iodofurans via palladium-catalyzed coupling and iodocyclization of terminal alkynes
Chen, Zhengwang,Huang, Gao,Jiang, Huanfeng,Huang, Huawen,Pan, Xiaoyan
experimental part, p. 1134 - 1139 (2011/04/24)
2,5-Disubstituted 3-iodofurans are readily prepared under very mild reaction conditions by the palladium/copper-catalyzed cross-coupling of (Z)-β-bromoenol acetates and terminal alkynes, followed by iodocyclization. The useful intermediates conjugated eny
