
Journal of Organometallic Chemistry p. 225 - 234 (1997)
Update date:2022-08-03
Topics:
Halterman, Ronald L.
Ramsey, Timothy M.
The coupling of enantiomerically enriched 2,2′-dilithio-1,1′-binaphthyl with various annulated cyclopentenones or 2-indanone proves to be a facile route for the preparation of a series of annulated bis(cyclopentadienes) or bis(indenes) bridged at a symmetrical cyclopentadienyl position. The six-or seven-membered annulated bis(tetrahydroindene) 6 or bis(hexahydroazulene) 7 ligands could readily be converted to titanium or zirconium dichloride complexes. Owing to the symmetry of the ligands, only a single C2-symmetrical isomer of the metallocene dichloride could form. Although the faces of the cyclopentadienyl moieties are homotopic, the chiral bridge enforces a chiral conformation of the metallocene complexes. The bis(indenyl) 5 or five-membered annulated bis(tetrahydropentalene) 8 ligands could not be metalated. Unbridged 2-methyl and 2-phenyl substituted tetrahydropentalenes 27 and 28 were prepared and could readily be converted to titanium dichloride complexes.
View MoreJurong Huaheng Natural Biological Products Factory
website:http://www.risebiochem.com
Contact:+86-13921007726
Address:Chuncheng town,Jurong city,Jiangsu province,China
website:http://www.NEM.COM.CN
Contact:+86-393-4411771
Address:The west section of shengli Road,Puyang,Henan Province,China
Contact:86-311-83160559
Address:shijiazhuang
NIGNXIA XINDACHANG TECHNOLOGY CO.,LTD
Contact:86-0951-7815345
Address:North side of Qiyuan Road, west side of Yuanfeng Highway, New Material Park, Ningdong Energy and Chemical Industry Base, Ningxia,China
Shanghai Sungo Technology Chemical Co., Ltd
Contact:0086-21-51385579
Address:Room2010, F/20, Tonghua Plaza, NO 345 Jinxiang Road, Jinqiao Export Processing Zone, Shanghai, 201206 P.R.CHINA
Doi:10.1021/jo01307a039
(1980)Doi:10.1021/jo01308a019
(1980)Doi:10.1002/adsc.202100234
(2021)Doi:10.1016/S0022-1139(00)81469-4
(1980)Doi:10.1002/jps.2600690237
(1980)Doi:10.1016/S0040-4039(01)85563-5
(1980)