Media controlled photo-Favorskii type rearrangement of α-chloro acetophenones: Synthesis of phenylacetic acids
DD Dhavale, VP Mali, SG Sudrik, HR Sonawane
Index: Dhavale, Dilip D.; Mali, Vasant P.; Sudrik, Surendra G.; Sonawane, Harikisan R. Tetrahedron, 1997 , vol. 53, # 49 p. 16789 - 16794
Full Text: HTML
Citation Number: 20
Abstract
Photolysis of substituted α-chloro acetophenones has been studied in different solvent systems wherein 1, 2-aryl migration is found to be media controlled. Effect of substituents on the migratory aptitude and a direct access to phenylacetic acids, in practical yields, has been described.
Related Articles:
[She, Meng-Yao; Xiao, Da-Wei; Yin, Bing; Yang, Zheng; Liu, Ping; Li, Jian-Li; Shi, Zhen Tetrahedron, 2013 , vol. 69, # 35 p. 7264 - 7268]
[Mineno, Tomoko; Hirayama, Haruyasu; Nakahara, Kazuhide; Yamashita, Mitsuaki; Kansui, Hisao; Moriwaki, Hiroshi Tetrahedron Letters, 2010 , vol. 51, # 46 p. 6045 - 6048]
[Rand,L.; Mohar,A.F. Journal of Organic Chemistry, 1965 , vol. 30, p. 3885 - 3888]
[Weinstock; Fuson Journal of the American Chemical Society, 1936 , vol. 58, p. 1233,1235]
[van Zanten,B.; Nauta,W. Recueil des Travaux Chimiques des Pays-Bas, 1960 , vol. 79, p. 1211 - 1222]