Journal of the Chemical Society. Perkin transactions I p. 726 - 735 (1981)
Update date:2022-07-30
Topics:
Lloyd, Douglas
Tucker, Kanwaljit S.
Marshall, Donald R.
A variety of 6-aryldihydrodiazepinium salts (including also 6-biphenyl-4-yl, 6-α-naphthyl, and 6-N-pyridyl) has been prepared, mostly by reactions of 1,2-diamines with 3-aryl-1,5-diazapentadienium salts.The electron-rich dihydrodiazepinium cation activates the 6-aryl substituent towards electrophilic attack, and halogenation and nitration take place at the p-position.Substituents vicinal to the ring junction in either the six- or seven-membered rings inhibit this reactivity, presumably by preventing coplanarity of the two rings; the 13C n.m.r. spectra of these vicinally substituted compounds also show the lowered electronic interactions between the rings.NN'-diphenyl and NN'-dibenzyl substituents also inhibit electrophilic substitution in the 6-phenyl ring.Solution in deuteriosulphuric acid generates a stable radical species.Nucleophiles (monoamines, diamines, sodium hydroxide) attack the 5- and 7-positions of the diazepine ring.The 13C n.m.r. and mass spectra of these compounds are discussed.
View MoreQINGDAO NEW FLOURISH INTERNATIOANAL TRADE CO., LTD.
Contact:+86 532 80861829
Address:No. 1, Yinchuan East Road, 266061, Qingdao, China
Shanghai Forever Synthesis Co.,Ltd.
Contact:021-61124658
Address:Zhoukang Road,Pudong New District,Shanghai,China
Shanghai Egoal Chemical Co.,Ltd
Contact:+86-21-50333091
Address:Yangming Garden Square 3,YangGao North Road 1188, Pudong New District, Shanghai
Golden Union Agrochemical Import and Export Co., Ltd.
Contact:86-755-23910527
Address:Room 1106, Tower 3A, Excellence Century Center, Futian District, Shenzhen, China
Beijing Harmony Chemical Co., Ltd.
Contact:86-010-84956928
Address:Room 207, Jin feng he B building, No 8 Xin Jie Kou Wai Street, Xi Cheng District, Beijing,PRC. 10008
Doi:10.1007/BF02218923
(1996)Doi:10.1002/ejoc.201901886
(2020)Doi:10.1021/jo00133a007
(1982)Doi:10.1016/j.ejmech.2017.01.036
(2017)Doi:10.1021/jo00133a032
(1982)Doi:10.1016/j.molcata.2016.10.035
(2017)
