A simple and efficient cationic Fe(III)/TEMPO-catalyzed oxidative cyclization of aroyl hydrazones has been developed for the synthesis of 2,5-disubstituted 1,3,4-oxadiazole derivatives. The reaction offers a broad scope, good functional-group tolerance, and high yields under mild conditions in the presence of O-2.
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Chiang Mai Univ, Fac Sci, Dept Chem, Chiang Mai 50200, ThailandChiang Mai Univ, Fac Sci, Dept Chem, Chiang Mai 50200, Thailand
Yamano, Dolnapa
Wiriya, Nittaya
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Chiang Mai Univ, Fac Sci, Dept Chem, Chiang Mai 50200, ThailandChiang Mai Univ, Fac Sci, Dept Chem, Chiang Mai 50200, Thailand
Wiriya, Nittaya
Phakhodee, Wong
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Chiang Mai Univ, Fac Sci, Dept Chem, Chiang Mai 50200, Thailand
Chiang Mai Univ, Fac Sci, Res Ctr Chem Dev Hlth Promoting Prod Northern Res, Chiang Mai 50200, ThailandChiang Mai Univ, Fac Sci, Dept Chem, Chiang Mai 50200, Thailand
Phakhodee, Wong
Wet-osot, Sirawit
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Minist Publ Hlth, Med Life Sci Inst, Dept Med Sci, Nonthaburi 11000, ThailandChiang Mai Univ, Fac Sci, Dept Chem, Chiang Mai 50200, Thailand
Wet-osot, Sirawit
Pattarawarapan, Mookda
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Chiang Mai Univ, Fac Sci, Dept Chem, Chiang Mai 50200, Thailand
Chiang Mai Univ, Fac Sci, Res Ctr Chem Dev Hlth Promoting Prod Northern Res, Chiang Mai 50200, ThailandChiang Mai Univ, Fac Sci, Dept Chem, Chiang Mai 50200, Thailand