1041850-10-5Relevant academic research and scientific papers
Rhenium-catalyzed coupling of 2-propynyl alcohols and several nucleophiles via dehydration
Kuninobu, Yoichiro,Ueda, Hirokazu,Takai, Kazuhiko
, p. 878 - 879 (2008)
Treatment of 2-propynyl alcohols with several nucleophiles in the presence of a catalytic amount of a rhenium complex, [ReBr(CO)3(thf)] 2, gave coupling products via dehydration. In these reactions, C-C, C-O, and C-S bonds can be con
SnCl2-catalyzed propargylic substitution of propargylic alcohols with carbon and nitrogen nucleophiles
Masuyama, Yoshiro,Hayashi, Miki,Suzuki, Noriyuki
, p. 2914 - 2921 (2013/07/05)
A weak Lewis acid, tin(II) chloride, which is insensitive to water and air, functioned as a catalyst for the propargylic substitution of secondary propargylic alcohols with carbon nucleophiles, such as electron-rich arenes, heteroarenes, and 1,3-dicarbony
Synthesis of tetrasubstituted furans via In-catalyzed propargylation of 1,3-dicarbonyl compounds-cyclization tandem process
Feng, Xunbo,Tan, Ze,Chen, De,Shen, Youming,Guo, Can-Cheng,Xiang, Jiannan,Zhu, Chengliang
, p. 4110 - 4112 (2008/09/21)
An efficient method to synthesize tetrasubstituted furans using simple starting materials such as propargylic alcohols and 1,3-dicarbonyl compounds has been developed. It was discovered that InCl3 could catalyze this transformation efficiently
