化学
试剂
戒指(化学)
药物化学
组合化学
立体化学
有机化学
作者
Masaki Shimizu,Masayuki Iwakubo,Yasushi Nishihara,Katsunari Oda,Tamejiro Hiyama
出处
期刊:Arkivoc
[ARKAT USA, Inc.]
日期:2006-10-15
卷期号:2007 (10): 29-48
被引量:2
标识
DOI:10.3998/ark.5550190.0008.a05
摘要
Treatment of 1,1,3,3-tetrakis(alkylthio)-2-silapropanes with t-BuLi in THF at -40 °C generated 1,1,3,3-tetrakis(alkylthio)-1,3-dilithio-2-silapropanes which reacted with various bifunctional chlorosilanes to give the corresponding 4-to 7-membered polysilacycloalkanes in moderate to good yields.Furthermore, double alkylation of the dilithiated silanes with bis(halomethyl)diorganosilanes or dihaloalkanes was found to proceed smoothly giving rise to 1,4-disilacyclohexanes or silacycloalkanes in good yields, respectively, in THF and an aprotic polar co-solvent such as hexamethylphosphoric triamide (HMPA) or 1,1,3,3-tetramethylurea (TMU).The sulfenyl groups in the cyclized products were smoothly removed by radical reduction with tributyltin hydride.
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