944940-51-6Relevant articles and documents
Regioselective synthesis of benzonitriles via amino-catalyzed [3+3] benzannulation reaction
Jiang, Lin,Jin, Wen-Fei,Yu, Liu-Dong,Yuan, Ming-Wei,Li, Hong-Li,Jiang, Deng-Bang,Yuan, Ming-Long
, p. 592 - 597 (2020/04/27)
A straightforward synthesis of benzonitriles is achieved via amino-catalyzed [3+3] benzannulation of α,β-unsaturated aldehydes and 4-arylsulfonyl-2-butenenitriles. Using pyrrolidine as an organocatalyst via iminium activation, a series of substituted benz
Electron-Deficient 3-Cyano-1-(p-toluenesulfonyl)-1,3-butadienes: Regio- and Stereoselective Synthesis of a Benzene Ring System by Michael-Type Addition-Cyclization with Enamines
Masuyama, Yoshiro,Yamazaki, Hideko,Toyoda, Yuko,Kurusu, Yasuhiko
, p. 964 - 967 (2007/10/02)
Knoevenagel-type condensation of 4-(p-toluenesulfonyl)-2-butenenitrile (1) with aldehydes provided electron-deficient 3-cyano-1-(p-toluenesulfonyl)-1,3-(E,Z)-butadienes 2, and one of these dienes, 2a was used in a Michael-type addition-cyclization with en