An iodophor-catalyzed sulfenylation of indoles using sulfonyl hydrazides as sulfur source to synthesize 3-sulfenylindoles in aqueous phase has been achieved. Notably, iodophor as catalyst and solvent is inexpensive, commercially available and no innocuous to the environment. The method is also easy to operate.
View Article and Find Full Text PDFA convenient and efficient strategy for the preparation of 2-sulfonylindoles has been achieved through iodophor-/HO-mediated 2-sulfonylation of indoles with readily available sulfonyl hydrazides in the aqueous phase. Iodophor is commercially available and serves as the green catalyst and aqueous phase. A series of 2-sulfonylated products from indoles and -methylpyrrole were synthesized in moderate yields in only 10 min.
View Article and Find Full Text PDFThe silicon atom in LSiCl or LSiMes (L = PhC(NBu), Mes = 2,4,6-MeCH) inserts into the B-X bond of RBX (R = Ph, Mes, N(SiMe); X = Cl, Br), which is followed by the migration of the amidinate ligand and the halide atom. By this way, LB(R)SiCl (R = Ph, ; Mes, ; N(SiMe), ) and LB(R)SiXMes (R = Ph, X = Cl, ; R = Mes, X = Cl, ; R = Mes, X = Br, ) were obtained. Furthermore, a silylene-borane adduct LClSi → BPhCl () was obtained as an intermediate in the formation of compound .
View Article and Find Full Text PDFCarbenes are known as donor molecules to form with chloroalane adducts, which enhances their aerobic and thermal stabilities. In contrast, the insertion products (cAACH)AlCl(cAAC) () and (cAACH)AlHCl(THF) (; THF = tetrahydrofuran) have been formed in the reaction of a cyclic alkyl(amino)carbene (cAAC:) with HAlCl and HAlCl, respectively. PhC(NBu)Li as the precursor for the reaction with HAlCl in a molar ratio of 2:1 can easily form compound [PhC(NBu)]AlH () with five-coordinate aluminum.
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