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dc.contributor.authorWong Phakhodeeen_US
dc.contributor.authorChuthamat Duangkamolen_US
dc.contributor.authorNitaya Wiriyaen_US
dc.contributor.authorMookda Pattarawarapanen_US
dc.description.abstract© 2018 The Royal Society of Chemistry. The first direct one-pot approach for the synthesis of N-substituted amidoximes from secondary amides or the intermediate amides has been developed. Through the Ph3P-I2-mediated dehydrative condensation, a variety of N-aryl and N-alkyl amidoximes (R1(CNOH)NHR2, where R1 or R2 = aryl, alkyl, or benzyl) were readily afforded under mild conditions and short reaction times. The synthetic application of the obtained amidoximes has also been demonstrated through the formation of 1,2,4-oxadiazolones via base-mediated carbonylative cyclization with 1,1′-carbonyldiimidazole.en_US
dc.subjectChemical Engineeringen_US
dc.titleA convenient one-pot synthesis of: N -substituted amidoximes and their application toward 1,2,4-oxadiazol-5-onesen_US
article.title.sourcetitleRSC Advancesen_US
article.volume8en_US Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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