17983-61-8Relevant articles and documents
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Neville
, p. 111 (1959)
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Sodium silylsilanolate enables nickel-catalysed silylation of aryl chlorides
Hitoshio, Kenshiro,Yamagishi, Hiroki,Shimokawa, Jun,Yorimitsu, Hideki
supporting information, p. 6867 - 6870 (2021/07/19)
Structurally diverse aryl chlorides were silylated with sodium silylsilanolate reagents in the presence of a Ni(cod)2catalyst complexed with a phosphine ligand; PMe2Ph for electron-rich substrates, and PCy2Ph for electron-deficient ones. The mild reaction conditions allowed the silylation of various aryl chlorides including functionalised drug molecules.
Dimethylformamide-stabilised palladium nanoclusters catalysed coupling reactions of aryl halides with hydrosilanes/disilanes
Nagata, Tatsuki,Inoue, Takeru,Lin, Xianjin,Ishimoto, Shinya,Nakamichi, Seiya,Oka, Hideo,Kondo, Ryota,Suzuki, Takeyuki,Obora, Yasushi
, p. 17425 - 17431 (2019/06/24)
N,N-Dimethylformamide-stabilised Pd nanocluster (NC) catalysed cross-coupling reactions of hydrosilane/disilane have been investigated. In this reaction, the coupling reaction proceeds without ligands with low catalyst loading. N,N-Dimethylacetamide is a crucial solvent in these reactions. The solvent effect was considered by various techniques, such as transmission electron microscopy, X-ray photoelectron spectroscopy, and thermogravimetric analysis. The Pd NCs can be recycled five times under both hydrosilane and disilane reaction conditions.