Silaheterocyclen: XI. Erzeugung und Cycloadditionsverhalten des Diphenylneopentylsilaethens, Ph2Si= CHCH2tBu
N Auner, W Ziche, E Herdtweck
Index: Auner, N.; Ziche, W.; Herdtweck, E. Journal of Organometallic Chemistry, 1992 , vol. 426, # 1 p. 1 - 22
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Citation Number: 31
Abstract
Abstract Diphenylneopentylsilene, Ph 2 Si= CHCH 2 t Bu (3), is prepared as a reactive intermediate by the reaction of diphenylvinylchlorosilane (1) with Li t Bu in nonpolar solvents via the α-lithioadduct Ph 2 Si (Cl) CH (Li) CH 2 t Bu (2). This lithiated species can be trapped by trimethylsilyltriflate and yields silene 3 by 1, 2-LiCl-elimination. Without suitable Si= C- trapping agents, the E/Z-isomeric tetraphenyl-2, 4-dineopentyl-1, 3-disilacyclobutane (6) is ...
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