A Microwave??Assisted Domino Benzannulation Reaction towards Functionalized Naphthalenes, Quinolines, and Isoquinolines

Y Wang, C Tan, X Zhang, Q He, Y Xie…

Index: Wang, Yuqin; Tan, Cun; Zhang, Xiaofei; He, Qian; Xie, Yuyuan; Yang, Chunhao European Journal of Organic Chemistry, 2012 , # 33 p. 6622 - 6629,8

Full Text: HTML

Citation Number: 3

Abstract

Abstract An efficient palladium/copper-catalyzed domino reaction was developed to yield functionalized naphthalenes, quinolines, and isoquinolines. The reactions of various substituted 1-phenylprop-2-yn-1-ols containing electron-donating (EDG) and electron- withdrawing (EWG) groups and 1-heteroarylprop-2-yn-1-ols worked well with this procedure. Both electron-rich and-deficient aryl halides were satisfactory substrates for this reaction. ...

Related Articles:

One-Pot Synthesis of Phthalazines and Pyridazino-aromatics: A Novel Strategy for Substituted Naphthalenes

[Oishi; Taido; Iwamoto; Miyashita; Higashino Chemical and Pharmaceutical Bulletin, 1990 , vol. 38, # 12 p. 3268 - 3272]

More Articles...