136638-69-2Relevant academic research and scientific papers
Indole functionalization via photoredox gold catalysis
Kaldas, Sherif J.,Cannillo, Alexandre,McCallum, Terry,Barriault, Louis
supporting information, p. 2864 - 2866 (2015/06/16)
The use of photoredox catalyst [Au2(dppm)2]Cl2 to initiate free-radical cyclizations onto indoles is reported. Excitation of the dimeric Au(I) photocatalyst for the reduction of unactivated bromoalkanes and bromoarenes is used for the generation of carbon-centered radicals. Previous to this work, reduction processes leading to indole functionalization utilizing photoredox catalysts were limited to activated benzylic or α-carbonyl-positioned bromoalkanes. This method offers a mild and safe alternative to organostannanes and pyrophoric initiators for access to high energy radicals that were previously inaccessible through catalytic or stoichiometric means.
N-fused indolines through non-carbonyl-stabilized rhodium carbenoid C-H insertion of N-aziridinyl imines
Mahoney, Stuart J.,Fillion, Eric
, p. 68 - 71 (2012/02/04)
Under rhodium catalysis, N-aziridinyl imines provided access to N-fused indolines through non-carbonyl-stabilized rhodium carbenoid C-H insertion. The utility of this methodology for the synthesis of architecturally complex heterocycles was further demonstrated by an expedient total synthesis of ( ±)-cryptaustoline (see scheme). Copyright
Radical cycloaddition by nickel(II) complex-catalyzed electroreduction. A method for preparation of pyrrolopyridine and pyrrolopyrrole derivatives
Ozaki, Shigeko,Mitoh, Shizue,Ohmori, Hidenobu
, p. 2020 - 2024 (2007/10/03)
Cycloalkano[a]pyrroles were obtained by reductive radical cycloaddition of 1-(2-iodoethyl)pyrrole and activated olefins or by cyclization of 1-(ω- iodoalkyl)pyrroles, through electroreduction of the iodides using nickel(II) complex as an electron-transfer catalyst.
HYDROGENATION OF COMPOUNDS CONTAINING AN INDOLIZINE MOIETY AND OF 1-BENZYLISOQUINOLINE OVER RHENIUM HEPTASULFIDE
Khorkhe, R. Alarkon,Soldatova, S. A.,Soldatenkov, A. T.,Ryashentseva, M. A.,Prostakov, N. S.
, p. 1253 - 1256 (2007/10/02)
It was shown by hydrogenation of 2,8-diphenylindolizine, benzoindolizine, dibenzoindolizine, dibenzoindolizine, 1-benzylisoquinoline, and 2,3-dimethyl-6-ethyl-4-(4-nitrophenyl)pyridine over Re2S7 (250 deg C, PH2 = 140 atm
