90653-68-2Relevant academic research and scientific papers
One-pot synthesis of 3-benzoyl- and 3-acetyl-1,2,4-oxadiazole derivatives using iron(III) nitrate
Itoh, Ken-Ichi,Sakamaki, Hiroshi,Horiuchi, C. Akira
, p. 1935 - 1938 (2005)
The reaction of nitriles and acetophenone with iron(III) nitrate at 80 °C gave the corresponding 3-benzoyl-1,2,4-oxadiazole derivatives. Moreover, in this reaction using acetone, the 3-acetyl-1,2,4-oxadiazole derivatives were obtained. Georg Thieme Verlag
Method of producing 1,2,4-oxadiazole derivatives
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Page/Page column 4, (2008/06/13)
A method for producing a 1,2,4-oxadiazol derivative represented by the formula (1): (1) [wherein, R1 represents a methyl group or a phenyl group, and R2 represents an optionally substituted linear or branched alkyl group], which comp
METHOD FOR PRODUCING 1,2,4-OXADIAZOL DERIVATIVE
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Page/Page column 9-10; 12-14, (2008/06/13)
A method for producing a 1,2,4-oxadiazol derivative represented by the formula (1): (1) [wherein, R1 represents a methyl group or a phenyl group, and R2 represents an optionally substituted linear or branched alkyl group], which comp
Mononuclear Heterocyclic Rearrangements. Part 11. Kinetic Study of the Rearrangement of (Z)-Phenylhydrazones of Some 5-Alkyl-3-benzoyl-1,2,4-oxadiazoles into 4-Acylamino-2,5-diphenyl-1,2,3-triazoles in Benzene, Dioxane-Water, and Acetonitrile
Frenna, Vincenzo,Vivona, Nicolo,Consiglio, Giovanni,Spinelli, Domenico
, p. 541 - 546 (2007/10/02)
The kinetics of the title reactions have been measured at various catalyst concentrations.The 5-alkyl-substituted phenylhydrazones (alkyl = Me, Et, Pri, or But) rearrange more slowly than the 5-H parent compound; moreover the rearran
