Bulletin of the Chemical Society of Japan p. 1875 - 1878 (1997)
Update date:2022-08-16
Topics:
Song, Yong-Qi
Yuzuri, Tomoaki
Suezawa, Hiroko
Sakakibara, Kazuhisa
Hirota, Minoru
Nakada, Masahiro
Photolyses of 2,6- and 2,4-difluorobromobenzenes in acetonitrile gave isomerized and brominated products in addition to 1,3-difluorobenzene produced by the dehalogenation.The reactions were compared with similar reactions of the corresponding chloro- and iodoarenes.In general, photolytic cleavage of the C-X bond of 2,6-difluorohalo(X)benzene was shown to proceed more easily than the corresponding 2,4-difluorohalo compound.
View More
Shanghai Longjin Metallic Material Co., Ltd.
website:http://www.shlongjin.cn/
Contact:021-56517503,56502257
Address:No.16, Lane 555, Chengyin Road, Shanghai
Contact:+86-20-32051076
Address:1105,Building A, International Business Incubator,Science City
Suzhou Howsine Biological Technology Co.,Ltd(expird)
website:http://www.howsine.com
Contact:86-512-67262751
Address:No 3,Weihua Road ,Suzhou Industrial Park ,Jiangsu ,China.
website:http://www.shtopchem.com/
Contact:0086-0576-87776998
Address:room no 1608,xuhui business building yude road,xujiahui street, xuhui district
HANGZHOU FOREWIN PHARMA CO., LTD
Contact:+86-571-89053961
Address:hangzhou
Doi:10.1111/j.1467-842X.2000.tb00508.x
(1928)Doi:10.3390/molecules16021825
(2011)Doi:10.1039/c9cc09466k
(2020)Doi:10.1021/j150576a048
(1959)Doi:10.1007/BF00564314
()Doi:10.1021/ic202342v
(2012)
