122981-89-9Relevant academic research and scientific papers
A Convenient Synthesis of 5-(1-Aminoalkyl)-1H-1,2,4-triazoles
Bruche, Luca,Garanti, Luisa,Zecchi, Gaetano
, p. 399 - 400 (2007/10/02)
5-(1-Aminoalkyl)-3-methoxycarbonyl-1-phenyl-1H-1,2,4-triazoles 5 were prepared from N-benzyloxycarbonyl-protected α-amino acids by reaction of the corresponding mixed anhydrides 2 with methyl phenylhydrazono(triphenylphosphoranylideneamino)acetate (3) and
Heterocycles as Masked Diamide/Dipeptide Equivalents. Formation and Reactions of Substituted 5-(Acylamino)oxazoles as Intermediates en route to the Cyclopeptide Alkaloids
Lipshutz, Bruce H.,Hungate, Randall W.,NcCarthy, Keith E.
, p. 7703 - 7713 (2007/10/02)
A variety of novel 2,4-dialkyl-5-(acylamino)oxazoles have been prepared by using either amide nitriles or diamides/dipeptides as starting materials.Ring closure calls for the use of trifluoroacetic acid/trifluoroacetic acid anhydride or an acid halide in
