
Journal of Organometallic Chemistry p. 173 - 181 (1990)
Update date:2022-08-02
Topics:
Weidenbruch, Manfred
Schaefers, Karen
Peters, Karl
Schnering, Hans Georg von
Treatment of di-t-butyldichlorostannane with sterically congested aryllithium compounds gives di-t-butylchloro(mesityl)stannane (2) and di-t-butylchloro(2,4,6-tri-t-butylphenyl)stannane (3), both of which show restricted rotation about the Sn-C(Ar) bond at room temperature.Reductive chloride elimination from 2 yields the corresponding distannane, whereas a similar reaction of 3 only results in decomposition.Reaction of 3 with t-butyllithium by hydrogen abstraction from one of the ortho-t-butylmethyl groups gives the stannaindane derivative (6).The structures of 3 and 6 have been confirmed by X-ray crystallography.
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Doi:10.1007/BF01168106
(1989)Doi:10.1007/s00726-010-0651-y
(2011)Doi:10.1134/S107042721012013X
(2010)Doi:10.1021/jo00299a020
(1990)Doi:10.1016/S0040-4020(01)89222-X
(1989)Doi:10.1016/j.poly.2019.02.027
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