硼氢化
硼烷
烯烃
化学
区域选择性
卡宾
硼烷
氢化物
取代基
药物化学
立体化学
金属
有机化学
硼
催化作用
作者
Chaohuang Chen,Constantin G. Daniliuc,Gerald Kehr,Gerhard Erker
标识
DOI:10.1002/chem.202301044
摘要
Abstract The neutral N‐heterocyclic carbene stabilized bora‐alkene 1 , conveniently prepared by a BH borenium/hydroboration route, forms stable copper, gold or palladium π‐complexes. The polar bora‐alkene B=C system undergoes regioselective hydroboration reactions with the (C 6 F 5 ) 2 BH or C 6 F 5 BH 2 ⋅ SMe 2 boranes. The latter reaction involves a subsequent rearrangement that leads to internal hydride vs. isothiocyanate substituent exchange at the borane pair.
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