124573-83-7Relevant academic research and scientific papers
A synthesis of α-amino acids via direct reductive carboxylation of imines with carbon dioxide
Sathe, Ajay A.,Hartline, Douglas R.,Radosevich, Alexander T.
supporting information, p. 5040 - 5042 (2013/06/05)
A method for the synthesis of α-amino acids by direct reductive carboxylation of aromatic imines with CO2 is described. The protocol employs readily available commercial reagents and serves as a one-step alternative to the Strecker synthesis. The Royal Society of Chemistry 2013.
Electrochemical carboxylation of fluorocontaining imines with preparation of fluorinated N-phenylphenylglycines
Koshechko,Titov,Bondarenko,Pokhodenko
, p. 701 - 706 (2008/12/22)
A possibility of obtaining fluorine-containing N-phenylphenylglycine derivatives at yields of up to 85% via the electrochemical carboxylation of corresponding benzalanilines was shown. The influence of imine's electron structure, the nature of supporting
Ugi four-component condensation with two cleavable components: the easiest synthesis of 2,N-diarylglycines
Faggi, Cristina,Neo, Ana G.,Marcaccini, Stefano,Menchi, Gloria,Revuelta, Julia
, p. 2099 - 2102 (2008/09/17)
The Ugi four-component condensation between anilines, aromatic aldehydes, isocyanides, and α-oxoacids afforded the expected adducts which were cleaved in mild conditions to give 2,N-diarylglycines in high yields.
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
