cheminform abstract: 1-(4-nitrophenyl)-4-phenyl-1h-1,2,3-triazole vs. 5(6)-nitrobenzofuroxan...

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ChemInform 2012, 43, issue 03 © 2012 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Triazole derivatives R 0280 DOI: 10.1002/chin.201203120 1-(4-Nitrophenyl)-4-phenyl-1H-1,2,3-triazole vs. 5(6)-Nitrobenzofuroxan Forma- tion and Their Antifungal Activity. — The synthesis of triazole derivatives (III) via Cu-catalyzed "click" reaction of corresponding nitrophenylazides (I) with phenyl- acetylene is attempted. p-Nitrophenyl azide (Ia) smoothly affords the desired triazole (IIIa), whilst in situ generated dinitrophenyl azide immediately gives nitrobenzo- furoxan (V). Compounds (I), (III) and (V) show good to excellent antifungal activities against Fusarium oxysporum. — (JAIN, M.; SHARMA, M.; GAUR, M.; ASHOK, T. D. S.; DUREJA, P.; ESWARAN*, S. V.; J. Indian Chem. Soc. 88 (2011) 4, 543-546 ; St. Stephen's Coll., Univ. Delhi, Delhi 110 007, India; Eng.) — C. Cyrus 03- 120

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Page 1: ChemInform Abstract: 1-(4-Nitrophenyl)-4-phenyl-1H-1,2,3-triazole vs. 5(6)-Nitrobenzofuroxan Formation and Their Antifungal Activity

Triazole derivativesR 0280 DOI: 10.1002/chin.201203120

1-(4-Nitrophenyl)-4-phenyl-1H-1,2,3-triazole vs. 5(6)-Nitrobenzofuroxan Forma-tion and Their Antifungal Activity. — The synthesis of triazole derivatives (III) via Cu-catalyzed "click" reaction of corresponding nitrophenylazides (I) with phenyl-acetylene is attempted. p-Nitrophenyl azide (Ia) smoothly affords the desired triazole (IIIa), whilst in situ generated dinitrophenyl azide immediately gives nitrobenzo-furoxan (V). Compounds (I), (III) and (V) show good to excellent antifungal activities against Fusarium oxysporum. — (JAIN, M.; SHARMA, M.; GAUR, M.; ASHOK, T. D. S.; DUREJA, P.; ESWARAN*, S. V.; J. Indian Chem. Soc. 88 (2011) 4, 543-546 ; St. Stephen's Coll., Univ. Delhi, Delhi 110 007, India; Eng.) — C. Cyrus

03- 120

ChemInform 2012, 43, issue 03 © 2012 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim