Intramolecular Hydrosilylation as a Route to 1-Aza-2,4-disilacyclobutanes
摘要:
[GRAPHICS]The addition of Pt catalyst to trisilyl-substituted amines results in the formation of intramolecular cyclization products, Unexpectedly, four-membered ring products are formed predominantly, rather than the thermodynamically more stable five-membered rings resulting from endo cyclization. The products are quite thermally stable and resist reaction with n-BuLi and n-BuLi/TMEDA, The trisilyl-substituted amine starting materials are prepared from lithium bis(silyl)amides and chlorosilanes in high yields.
Intramolecular Hydrosilylation as a Route to 1-Aza-2,4-disilacyclobutanes
摘要:
[GRAPHICS]The addition of Pt catalyst to trisilyl-substituted amines results in the formation of intramolecular cyclization products, Unexpectedly, four-membered ring products are formed predominantly, rather than the thermodynamically more stable five-membered rings resulting from endo cyclization. The products are quite thermally stable and resist reaction with n-BuLi and n-BuLi/TMEDA, The trisilyl-substituted amine starting materials are prepared from lithium bis(silyl)amides and chlorosilanes in high yields.