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Me<sub>3</sub>SiSiMe<sub>2</sub>(O<sup><i>n</i></sup>Bu): a disilane reagent for the synthesis of diverse silacycles <i>via</i> Brook- and retro-Brook-type rearrangement

Yankun Xu, Weiwei Xu, Xinyang Chen, Xiai Luo, Haiyan Lu, Minghao Zhang, Xiumei Yang, Guobo Deng, Yun Liang, Yuan Yang

2021Chemical Science36 citationsDOIOpen Access PDF

Abstract

the cleavage of Si-Si, Si-C, and Si-O bonds, leading to the formation of spirobenzosiloles, fused benzosiloles, and π-conjugated dibenzosiloles in moderate to good yields. Preliminary mechanistic studies indicate that this transformation is realized by successive palladium-catalyzed bis-silylation and Brook- and retro-Brook-type rearrangement of silane-tethered silanols.

Topics & Concepts

DisilaneReagentType (biology)ChemistryPhysical chemistryOrganic chemistrySiliconGeologyPaleontologyOrganoboron and organosilicon chemistryCatalytic Cross-Coupling ReactionsSynthesis and characterization of novel inorganic/organometallic compounds
Me<sub>3</sub>SiSiMe<sub>2</sub>(O<sup><i>n</i></sup>Bu): a disilane reagent for the synthesis of diverse silacycles <i>via</i> Brook- and retro-Brook-type rearrangement | Litcius