79841-63-7Relevant articles and documents
Hydrocarbon-Soluble Bis(trimethylsilylmethyl)calcium and Calcium-Iodine Exchange Reactions at sp2-Hybrized Carbon Atoms
Koch, Alexander,Wirgenings, Marino,Krieck, Sven,G?rls, Helmar,Pohnert, Georg,Westerhausen, Matthias
, p. 3981 - 3986 (2017/10/31)
Hydrocarbon-soluble and highly reactive [(L)xCa(CH2SiMe3)2] (L = tetrahydropyran, x = 4 (2a); L = tmeda, x = 2 (2b)) is synthesized by the metathesis reaction of Me3SiCH2CaI (1-I) with KCH2SiMe3. The durability of 2a in tetrahydropyran solution at 0 °C is sufficiently high for subsequent chemical transformations. The reaction of ICH2SiMe3 with calcium in diethyl ether yields unique cage compound [(Et2O)2Ca(I)2·(Et2O)2Ca(I)(OEt)·(Et2O)Ca(I)(CH2SiMe3)] (3). We demonstrate that alkylcalcium complexes are valuable reagents for calcium-iodine exchange reactions at Csp2-I functionalities.
Synthesis and Chemical Behaviour of Thioacylsilanes (Silyl Thioketones). Part 1. Oxidation to S-Oxides, Conversion into Silylated Thiiranes, Silylated Triarylethylenes, and α-Silylated Sulphides
Barbaro, Gaetano,Battaglia, Arturo,Giorgianni, Patrizia,Maccagnani, Gaetano,Macciantelli, Dante,et al.
, p. 381 - 386 (2007/10/02)
Trimethylsilyl and triphenylsilylaryl thioketones have been synthesized by acid catalysed reaction of the corresponding ketones with hydrogen sulphide.Such silylated thioketones heve been oxidized to give S-oxides and converted with diaryldiazomethanes into triaryl thiiranes; upon treatment with organolithium nucleophiles they undergo thiophilic addition.The ready desulphurization with triphenylphosphine of silylated thiirans to the corresponding silyl triaryl ethylenes is also reported.
Silyl Thioketones and Silylated Thiirans
Bonini, Bianca F.,Mazzanti, Germana,Sarti, Sauro,Zanirato, Paolo,Maccagnani, Gaetano
, p. 822 - 823 (2007/10/02)
The preparation of silyl thioketones, and their reactions leading to silylated thiirans and other hitherto unknown silylated heterocycles, are reported.