• Bulletin of the Korean Chemical Society
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• v.22 no.10
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• pp.1153-1155
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• 2001

• Bulletin of the Korean Chemical Society
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• v.30 no.11
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• pp.2812-2814
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• 2009

• Journal of the Korean Chemical Society
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• v.53 no.2
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• pp.159-165
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• 2009

The synthesis of 2-amino-5-substituted-1,3,4-oxadiazoles 4 were carried out from the electrooxidation of semicarbazone 3 at the platinum electrode under controlled potential electrolysis in an undivided cell. This is an environmentally benign method in the field of synthetic organic chemistry. The non-aqueous solvents acetic acid and acetonitrile and a supporting electrolyte lithium perchlorate were used for the electrolysis in the electrooxidation. The products were structurally charecterised by IR, $^1H$-NMR, $^{13}C$-NMR and elemental analysis.

• Journal of the Korean Chemical Society
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• v.48 no.2
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• pp.177-181
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• 2004

1,2,4-Triazoles, pyrazolones and 1,3,4-oxadiazoles have been synthesized from substituted hydrazide using various solid supports under microwave irradiation (MWI). The results obtained highlight the versatility of the solid supports. All synthesized compounds were screened for their antifungal activity against A. niger and A. flavus and were found to possess good activity.

• Bulletin of the Korean Chemical Society
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• v.33 no.11
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• pp.3701-3705
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• 2012

A simple method has been developed for four-component synthesis of disubstituted 1,3,4-oxadiazoles using (N-isocyanimino)triphenylphosphorane, a primary amine, a carboxylic acid and biacetyl in $CH_2Cl_2$ by the Ugi-4CR/aza-Wittig sequence at room temperature in excellent yields.

• Journal of the Korean Chemical Society
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• v.54 no.5
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• pp.582-588
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• 2010

The synthesis of benzofuran based 1,3,4-thiadiazoles, 1,3,4-triazoles and 1,3,4-oxadiazole via cyclocondensation of thiosemicarbazides have been carried out by conventional and non-conventional methods in excellent yields of product.

• Archives of Pharmacal Research
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• v.24 no.4
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• pp.263-269
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• 2001

Diazepamoxadiazoles 4,5,6,12,14 and 22 were prepared with the binary form system. Diazepamthiadiazoles 15,20 and Diazepamtriazoles 7,8,9,17,18,19 and 21 were also shapely synthesized. Some of these compounds were screened to test their antibacterial activity against E. coli and B. subtilis compounds 15 and 20 show potent activity against these bacteria.

• Archives of Pharmacal Research
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• v.20 no.6
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• pp.602-609
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• 1997

A new series of 1, 3, 4-oxadiazoles, 1, 3, 4-thiadiazoles and 1, 2, 4-triazoles incorporated directly and/or indirectly into a xanthenone moiety at position-2-were synthesized. Some of the newly prepared compounds were biologically tested as schistosomicides in experimental animals.

• Journal of the Korean Chemical Society
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• v.54 no.1
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• pp.59-64
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• 2010

The synthesis of a series of fluorinated thiadiazoles 3, triazoles 4 and oxadiazoles 5 are synthesized from thiosemicarbazides 2 containing (2-(6-methyl-2-p-tolyl-lH-imidazo[1,2-a]pyridin-3-yl nucleus. These reactions were carried out by conventional method as well as ultra sound irradiation method. All products have been characterized by IR, 1H NMR, MS study and screened for their antimicrobial activity.

• Journal of the Korean Chemical Society
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• v.15 no.3
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• pp.121-125
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• 1971

Tere-and Isophthalohydroxamoyl chlorides were condensed with 1, 4-benzoquinone to afford quinone type polymer with the oxidation of the ring structure. Similarly, tere-and isophthalohydroxamoyl chlorides were condensed with tere-and isophthaldioximes and terephthalonitrile to give crystalline polyphenylene-1,2,4-oxadiazoles, among which the reaction product of terephthalohydroxamoyl chloride with terephthalonitrile in xylene afforded the highest crystallinity.