155140-69-5Relevant academic research and scientific papers
Gold-Catalyzed Highly Selective Photoredox C(sp2)-H Difluoroalkylation and Perfluoroalkylation of Hydrazones
Xie, Jin,Zhang, Tuo,Chen, Fei,Mehrkens, Nina,Rominger, Frank,Rudolph, Matthias,Hashmi, A. Stephen K.
, p. 2934 - 2938 (2016)
The first gold-catalyzed photoredox C(sp2)-H difluoroalkylation and perfluoroalkylation of hydrazones with readily available RF-Br reagents is reported. The resulting gem-difluoromethylated and perfluoroalkylated hydrazones are highl
Perfluoroalkylation of Aryl-N,N-dimethyl Hydrazones Using Hypervalent Iodine(III) Reagents or Perfluoroalkyl Iodides
Janhsen, Benjamin,Studer, Armido
, p. 11703 - 11710 (2017/11/24)
Radical trifluoromethylation of aryl N,N-dimethyl hydrazones using TBAI as an initiator and Togni's reagent as a trifluoromethyl radical source is described. Cascades proceed via electron-catalysis; this approach is generally more applicable to hydrazone perfluoroalkylation using perfluoroalkyl iodides as the radical precursors in combination with a base under visible-light initiation.
Hydrazone as the directing group for Ir-catalyzed arene diborylations and sequential functionalizations
Ros, Abel,Lopez-Rodriguez, Rocio,Estepa, Beatriz,Alvarez, Eleuterio,Fernandez, Rosario,Lassaletta, Jose M.
supporting information; experimental part, p. 4573 - 4576 (2012/04/23)
The use of hemilabile pyridine-hydrazone N,N-ligands allows the highly selective Ir-catalyzed ortho,ortho'-directed diborylation of aromatic N,N-dimethylhydrazones in near-quantitative yields. One-pot sequential Suzuki-Miyaura cross-coupling with different aryl bromides provides a short entry to unsymmetrically substituted 2,6-diarylbenzaldehyde derivatives.
Use of hemilabile N,N ligands in nitrogen-directed iridium-catalyzed borylations of arenes
Ros, Abel,Estepa, Beatriz,Lopez-Rodriguez, Rocio,Alvarez, Eleuterio,Fernandez, Rosario,Lassaletta, Jose M.
supporting information; experimental part, p. 11724 - 11728 (2012/02/14)
The hemilabile character of 2-pyridyl carbaldehyde hydrazones as N,N bidentate ligands is key to performing regioselective IrIII-catalyzed ortho borylations of 2-aryl pyridines(isoquinolines) and aromatic N,N-dimethylhydrazones (see scheme; pin=pinacol, Bn=benzyl). Internal "ate" complexes or products free from N-B interactions are formed depending on the steric properties of the substrates. Copyright
