
Australian Journal of Chemistry p. 2379 - 2383 (1984)
Update date:2022-09-26
Topics:
Wilson, Michael A.
Rottendorf, Horst
Collin, Philip J.
Vasallo, Anthony M.
It has been shown that the reaction of aluminium chloride with tetralin yields 6,6'-(butane-1,4-diyl)-bis(1,2,3,4-tetrahydronaphthalene) as well as a number of other products.It is suggested that this compound is formed by protonation of tetralin, fragmentation of the alicyclic ring and then electrophilic attack of a further tetralin molecule.The positions of substitution in the product suggests that ion pairs are involved in the reaction.It is clear that intermediates have sufficient lifetime to undergo intermolecular substitution reactions in addition to intramolecular substitution or proton loss.
View MoreYanCheng LongShen Chemical Co.,Ltd.
Contact:+86-515-86668866
Address:No.13,Weiyi Road,Funing Aoyang Industrial Park
Contact:+86-717-6370352
Address:168 Chengdong Avenue, Yichang, Hubei 443003, P. R.China
Contact:+86-519-86339586,13584329896
Address:Changzhou Scientific and Education Park
Shenzhen Feiming Science and Technology Co,. Ltd
Contact:+86-755-85232577
Address:#B2309, Fenglin International Center ,Jixiang Road, Longcheng street, LongGang District, Shenzhen city, Guangdong province, China.
Zhengzhou Institute of Chiral Pharmer Research Co., Ltd.
Contact:86-371-55219111
Address:15 Floor, 2 Building, Central China Technovalley, Zhongyuan West Road
Doi:10.1021/jo981420y
(1998)Doi:10.1016/S0277-5387(97)00178-2
(1997)Doi:10.1021/jo980248v
(1998)Doi:10.1016/S0040-4039(97)00938-6
(1997)Doi:10.1002/cbic.200900723
(2010)Doi:10.1021/jm970170v
(1997)