859331-05-8Relevant academic research and scientific papers
Cu-catalyzed intramolecular hydroarylation of alkynes
Wang, Yun-Long,Zhang, Wen-Man,Dai, Jian-Jun,Feng, Yi-Si,Xu, Hua-Jian
, p. 61706 - 61710 (2015/02/19)
An efficient Cu-catalyzed intramolecular hydroarylation reaction of alkynes has been developed. The reaction is accomplished under mild conditions and shows good tolerance to both electron-rich and electron-deficient aryl nucleophiles. A series of aryl, h
General synthesis of 8-aryl-2-tetralones
Carreno, M. Carmen,Gonzalez-Lopez, Marcos,Latorre, Alfonso,Urbano, Antonio
, p. 4956 - 4964 (2007/10/03)
Two alternative routes are described for the synthesis of 8-aryl-2-tetralones (1). Route A starts from α-tetralone 3 and involves 3 or 4 steps, with the selective Na-EtOH reduction of 1-aryl-7-methoxynaphthalenes 2 being the key step. The exclusive reduct
Ring selectivity in the Na/EtOH reduction of 1-aryl-7-methoxynaphthalenes
Carre?o, M. Carmen,González-López, Marcos,Latorre, Alfonso,Urbano, Antonio
, p. 1601 - 1605 (2007/10/03)
Na/EtOH reduction of 1-aryl-7-methoxynaphthalenes occurred preferentially at the A-ring when no substituents were present at the ortho-positions of the aryl group (up to 100% selectivity), to afford 1-aryl-7-methoxy-1,2,3,4- tetrahydronaphthalenes. Ortho-
