1049796-79-3Relevant academic research and scientific papers
Highly efficient synthesis of functionalized dihydronaphthalenes, tetrahydronaphthalenes, and tetrahydroisoquinolines by iron-catalyzed intramolecular Friedel-Crafts reaction of aryl-containing propargylic alcohols
Huang, Wen,Hong, Longcheng,Zheng, Pengzhi,Liu, Ruiting,Zhou, Xigeng
body text, p. 3603 - 3610 (2009/09/06)
An efficient, convenient, and one-pot procedure for the synthesis of a series of new dihydro- and tetrahydronaphthalenes as well as tetrahydroisoquinolines has been established through Lewis acid-catalyzed intramolecular Friedel-Crafts reaction of aryl-substituted propargylic alcohols.
Controllable one-step synthesis of spirocycles, polycycles, and di- and tetrahydronaphthalenes from aryl-substituted propargylic alcohols
Huang, Wen,Zheng, Pengzhi,Zhang, Zhengxing,Liu, Rutting,Chen, Zhenxia,Zhou, Xigeng
, p. 6845 - 6848 (2008/12/22)
(Chemical Equation Presented) A novel, convenient, and efficient method has been developed for selective synthesis of spirocycle, polycycle, and di-and tetrahydronaphthalene systems from aryl-substituted propargylic alcohols by FeCl3- or TsOH-catalyzed multiple activations of unsaturated C-C bonds and C-H bonds.
