
Journal of Organometallic Chemistry p. 411 - 417 (1992)
Update date:2022-08-11
Topics:
Nakadaira, Yasuhiro
Sato, Ryuji
Sakurai, Hideki
The first preparations of C-unsubstituted stannacycloheptatriene and germacycloheptatriene, analogues of cycloheptatriene, are described with their spectroscopic properties.A stannacyclohexadienyl anion derived from stannacyclohexadiene by treatment with lithium di-isopropylamide was allowed to react with chlorocarbene generated from dichloromethane and n-butyllithium, and this led to the formation of the corresponding stannacycloheptatriene.The disproportionation reaction between the stannacyclohexadiene and dichlorodimethylgermane gave the corresponding germacyclohexadiene in reasonable yield.In a similar manner, the reaction of the germacyclohexadienyl anion with chlorocarbene yielded C-unsubstituted germacycloheptatriene.
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