27376-57-4Relevant articles and documents
The reactions of the ozonides with secondary amines: An efficient and novel way to prepare tertiary amine from mono- and 1,1-di-substituted alkenes via corresponding ozonides
Hon, Yung-Son,Lu, Ling
, p. 5309 - 5312 (1993)
The ozonolysis of mono- and 1,1-di-substituted olefins followed by treatment with secondary amines in the presence of 4A, molecular sieves to give the corresponding tertiary amine in high yields. This transformation involved four sequential reactions in the same flask.
Iron-catalyzed chemoselective hydride transfer reactions
Coufourier, Sébastien,Ndiaye, Daouda,Gaillard, Quentin Gaignard,Bettoni, Léo,Joly, Nicolas,Mbaye, Mbaye Diagne,Poater, Albert,Gaillard, Sylvain,Renaud, Jean-Luc
supporting information, (2021/06/07)
A Diaminocyclopentadienone iron tricarbonyl complex has been applied in chemoselective hydrogen transfer reductions. This bifunctional iron complex demonstrated a broad applicability in mild conditions in various reactions, such as reduction of aldehydes over ketones, reductive alkylation of various functionalized amines with functionalized aldehydes and reduction of α,β-unsaturated ketones into the corresponding saturated ketones. A broad range of functionalized substrates has been isolated in excellent yields with this practical procedure.
Kn?lker's iron complex: An efficient in situ generated catalyst for reductive amination of alkyl aldehydes and amines
Pagnoux-Ozherelyeva, Anastassiya,Pannetier, Nicolas,Mbaye, Mbaye Diagne,Gaillard, Sylvain,Renaud, Jean-Luc
supporting information; experimental part, p. 4976 - 4980 (2012/06/30)
An aminated series: A well-defined iron-catalyzed reductive amination reaction of aldehydes and ketones with aliphatic amines using molecular hydrogen is presented. Under mild conditions, good yields for a broad range of alkyl ketones as well as aldehydes were achieved. Copyright
