Ultrasound-promoted synthesis of 3-trichloromethyl-5-alkyl(aryl)-1,2,4-oxadiazoles.

[1]  A. Flores,et al.  Ultrasound promoted synthesis of thioesters from 2-mercaptobenzoxa(thia)zoles. , 2010, Ultrasonics sonochemistry.

[2]  Ling Li,et al.  A convenient and efficient protocol for the synthesis of 5-aryl-1,3-diphenylpyrazole catalyzed by hydrochloric acid under ultrasound irradiation. , 2010, Ultrasonics sonochemistry.

[3]  F. Quina,et al.  Efficient sonochemical synthesis of novel 3,5-diaryl-4,5-dihydro-1H-pyrazole-1-carboximidamides. , 2010, Ultrasonics sonochemistry.

[4]  M. Martins,et al.  Preparation of trichloroacetoamidoxime in aqueous media and application in one pot synthesis of 1,2,4-oxadiazoles , 2009 .

[5]  R. Srivastava,et al.  First ultrasound-mediated one-pot synthesis of N-substituted amides. , 2009, Ultrasonics sonochemistry.

[6]  P. Alagarsamy,et al.  PTSA-ZnCl2: an efficient catalyst for the synthesis of 1,2,4-oxadiazoles from amidoximes and organic nitriles. , 2009, The Journal of organic chemistry.

[7]  J. Guedes,et al.  An easy synthesis of 3,5-disubstituted 1,2,4-oxadiazoles from carboxylic acids and arylamidoximes mediated by ethyl chloroformate , 2009 .

[8]  V. Sureshbabu,et al.  Synthesis of 1,2,4-oxadiazole-linked orthogonally urethane-protected dipeptide mimetics , 2008 .

[9]  A. P. Piccionello,et al.  Synthesis of fluorinated first generation starburst molecules containing a triethanolamine core and 1,2,4-oxadiazoles , 2006 .

[10]  M. Adib,et al.  Microwave-assisted efficient, one-pot, three-component synthesis of 3,5-disubstituted 1,2,4-oxadiazoles under solvent-free conditions , 2006 .

[11]  Sarah A. Norring,et al.  Convergent, parallel synthesis of a series of β-substituted 1,2,4-oxadiazole butanoic acids as potent and selective αvβ3 receptor antagonists , 2006 .

[12]  R. Srivastava,et al.  Synthesis of 3-aryl-5-decapentyl-1,2,4-oxadiazoles possessing antiinflammatory and antitumor properties. , 2005, Farmaco.

[13]  R. Braga,et al.  A mild and efficient method for halogenation of 3,5-dimethyl pyrazoles by ultrasound irradiation using N-halosuccinimides , 2005 .

[14]  Jean‐François Hernandez,et al.  Synthesis of Various 3-Substituted 1,2,4-Oxadiazole-Containing Chiral β3- and α-Amino Acids from Fmoc-Protected Aspartic Acid , 2003 .

[15]  A. Tartar,et al.  Parallel synthesis of 1,2,4-oxadiazoles from carboxylic acids using an improved, uronium-based, activation , 2001 .

[16]  R. Srivastava,et al.  Synthesis, anti-inflammatory and antimicrobial activities of new 1,2,4-oxadiazoles peptidomimetics. , 2000, Farmaco.

[17]  G. Liang,et al.  An improved oxadiazole synthesis using peptide coupling reagents , 1996 .

[18]  Alan R. Katritzky,et al.  Comprehensive Heterocyclic Chemistry IV , 1996 .

[19]  D. Spinelli,et al.  Studies on azole-to-azole interconversions. Substituent effects on the ring-degenerate equilibration between 3-aroylamino-5-methyl-1,2,4-oxadiazoles and 3-acetylamino-5-aryl-1,2,4-oxadiazoles , 1995 .