
Bulletin of the Chemical Society of Japan p. 3607 - 3612 (1987)
Update date:2022-08-02
Topics: 1H NMR 13C NMR Substituent Effects
Suda, Kohji
Tsujimoto, Toshio
Yamauchi, Masashige
Substituent effects on the chemical shifts of the conjugation sites in α-phenyl-N-arylnitrones (2) have been investigated.Resonance effects predominate at these positions.The electronic effects of the substituents should be treated separately between electron-donating groups and electron-donating groups and electron-withdrawing ones.A plausible mechanism for the transmission of substituent effects in 2 has been proposed.
View Moreshanghai Tauto Biotech Co., Ltd
website:http://www.tautobiotech.com/en/index.htm
Contact:+86-21-51320588 ext. 8025
Address:No. 326, Aidisheng Rd , Zhangjiang Hi-tech Park, Shanghai , P.R.CHINA
QINGDAO TAOSIGN INTERNATIONAL TRADE CO.,LIMITED
Contact:+86-0532-82683616
Address:RM1402, Doublestar Seacoase 7#, No. 5 Guizhou Road, Qingdao, Shandong, China
Anhui Jiatiansen Agrochemical Co.,Ltd
Contact:15366811918
Address:chemical industrial park,xiangyu town,dongzhi county,anhui,china
Contact:21-7631221 15884421033
Address:326 Science and technology,Shanghai,China
Zhejiang Chemicals Import & Export Corporation (ZHECHEM)
Contact:+86-571-87046953
Address:No. 37, Qingchun Road
Doi:10.1021/om4009058
(2013)Doi:10.1016/j.tet.2007.06.042
(2007)Doi:10.1007/BF00630244
(1992)Doi:10.1016/j.dyepig.2013.01.016
(2013)Doi:10.1021/ja01499a092
(1960)Doi:10.1039/b705684b
(2007)