124573-72-4Relevant articles and documents
Radical Rearrangement of Aryl/Alkylidene Malononitriles via Aza Michael Addition/Decynoformylation/Addition Sequence: An Access to α-Aminonitriles and α-Aminoamides
Bhoite, Shubhangi P.,Bansode, Ajay H.,Suryavanshi, Gurunath
, p. 14858 - 14865 (2020)
An efficient, safe, and environmentally friendly tertiary butyl hydrogen peroxide (TBHP)-mediated rearrangement of aryl/alkylidene malononitrile with anilines has been developed with in situ generation of HCN as the cyanide source for the synthesis of sub
Synthesis, spectroscopic characterization, X-ray analysis and theoretical studies on the spectral features (FT-IR, 1H-NMR), chemical reactivity, NBO analyses of 2-(4-fluorophenyl)-2-(4-fluorophenylamino)acetonitrile and its docking into IDO enz
Brahmachari, Goutam,Kumar, Abhishek,Srivastava, Ambrish Kumar,Gangwar, Shashi,Misra, Neeraj,Gupta, Vivek K.,Rajnikant
, p. 80967 - 80977 (2015)
A new fluorinated α-aminonitrile compound, namely, 2-(4-fluorophenyl)-2-(4-fluorophenylamino)acetonitrile (C14H10F2N2), has been synthesized following a 'green protocol' and characterized on the basis of its ele
Open-Chain Reissert Compounds: One-Pot Synthesis and Utility in Synthesis of Unsymmetrical Imides, α-Acylamino Carboxamides, Imidazolinones, and Hydantoins
Leblanc, Jean-Pierre,Gibson, Harry W.
, p. 1072 - 1077 (2007/10/02)
Acyclic Reissert compounds 2 and bis(Reissert compound)s 3-5 can be conveniently prepared in a biphasic system without isolation of the intermediate α-amino nitriles.Treatment of 2 with sodium hydride affords substituted unsymmetrical imides as 8.Oxidativ
Synthesis of Some New 3,4-Diarylsydnones
Csongar, Ch.,Mueller, I.,Slezak, H.,Klebsch, H.-J.,Tomaschewski, G.
, p. 1006 - 1014 (2007/10/02)
The synthesis of some new sydnones 4 is described.Their characteristic absorption maxima, mass spectroscopic fragmentation and C=O-valence vibrations are given.The sydnones 4 are synthezid by nitrosation of C,N-diarylglycines 3 (from strecker synthesis) a