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Volumn 50, Issue , 2012, Pages 39-43

Synthesis of new α aminophosphonate system bearing Indazole moiety and their biological activity

Author keywords

Aminophosphonates; Antibacterial; Biological active compounds; Imines; Indazole derivatives; Synthesis

Indexed keywords

1 METHYL N (2 NITROBENZYLIDENE) 1H INDAZOLE 3 CARBOHYDRAZIDE; 1 METHYL N [4 (TRIFLUOROMETHYL)BENZYLIDENE] 1H INDAZOLE 3 CARBO HYDRAZIDE; ALPHA AMINOPHOSPHONATE; ANTIINFECTIVE AGENT; CHLOROTRIMETHYLSILANE; DIETHYL(2 (1 METHYL 1H INDAZOLE 3 CARBONYL)HYDRAZINYL)(2 NITROPHENYL)METHYLPHOSPHONATE; DIETHYL(2 CHLOROPHENYL)[2 (1 METHYL 1H INDAZOLE 3 CARBONYL)HYDRAZINYL]METHYLPHOSPHONATE; DIETHYL(3 FLUOROPHENYL)[2 (1 METHYL 1H INDAZOLE 3 CARBONYL)HYDRAZINYL]METHYL PHOSPHONATE; DIETHYL[2 (1 METHYL 1H INDAZOLE 3 CARBONYL)HYDRAZINYL](PHENYL)METHYL PHOSPHONATE; DIETHYL[2 (1 METHYL 1H INDAZOLE 3 CARBONYL)HYDRAZINYL][4 (TRIFLUORO)PHENYL]METHYLPHOSPHONATE; INDAZOLE DERIVATIVE; N (2 BROMOBENZYLIDENE) 1 METHYL 1H INDAZOLE 3 CARBOHYDRAZIDE; N (2 CHLOROBENZYLIDENE) 1 METHYL 1H INDAZOLE 3 CARBOHYDRAZIDE; N (3 FLUOROBENZYLIDENE) 1 METHYL 1H INDAZOLE 3 CARBOHYDRAZIDE; N (4 BENZYLIDENE 1 METHYL 1H INDAZOLE 3 CARBO HYDRAZIDE; N BENZYLIDENE 1 METHYL 1H INDAZOLE 3 CARBOHYDRAZIDE; PHOSPHITE; TRIETHYL PHOSPHITE; UNCLASSIFIED DRUG;

EID: 84858442522     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2012.01.024     Document Type: Article
Times cited : (59)

References (40)
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    • (2002) Science of Synthesis: Indazoles , pp. 227-324
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  • 23
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.