127279-63-4Relevant academic research and scientific papers
Diastereoselective synthesis of C3-quaternary indolenines using α,β-unsaturated N-aryl ketonitrones and activated alkynes
Huehls, C. Bryan,Hood, Tyler S.,Yang, Jiong
supporting information; experimental part, p. 5110 - 5113 (2012/07/03)
New trick for an old dog: C3-Quaternary indolenines were synthesized by combining readily available α,β-unsaturated N-aryl ketonitrones and activated alkynes. This remarkably simple and atom-economical transformation does not require transition-metal cata
N-Allylhydroxylamines from 1,2-Addition of Allyl Grignard Reagents to Nitro Compounds: Generality and Drawbacks of the Reaction
Barboni, Luciano,Bartoli, Giuseppe,Marcantoni, Enrico,Petrini, Marino,Dalpozzo, Renato
, p. 2133 - 2138 (2007/10/02)
Allyl Grignard reagents react with both aromatic and aliphatic nitro derivatives via 1,2-addition to the nitro group.Conversely, nitroalkanes give either intractable mixtures or exclusively 1,4-conjugate addition.Nitroarenes with high steric hindrance at the ortho position and low aromatic stabilisation give competive or exclusive conjugate addition at the reactive para position.The 'in situ' treatment of the unstable 1,2-adducts with aluminium hydrides in the presence of catalytic amounts of palladium on charcoal provides a general method of synthesis ofN-allylhydroxylamines.LiAlH4 is a very efficient reducing agent, but, in some cases, it does not allow the reduction to be stopped at the hydroxylamino stage.Red-Al and DIBAL-H are less efficient but they ensure greater selectivity.Red-Al avoids the complete reduction to amines except when a strongly electron-donating substituent such as a methoxy group is present in the para position of the aromatic ring.Hydroxylamines can be obtained by reaction of nitrosoarenes followed by aqueous quenching.However, this alternative reaction does not offer any improvement, since relevant amounts of azo and azoxy derivatives are recovered as by-products.
