Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Makbule Maden"'
Publikováno v:
Journal of the Serbian Chemical Society, Vol 75, Iss 12, Pp 1625-1635 (2010)
1-(3-Aminophenyl)-4-benzoyl-5-phenyl-1H-pyrazole-3-carboxylic acid (1) was synthesized according to the literature. 2-(3-Aminophenyl)-2,6-dihydro-3,4-diphenyl-7H-pyrazolo[3,4-d]pyridazin-7-one (5) was obtained by the cyclocondensation reaction of 1 w
Externí odkaz:
https://doaj.org/article/daf287e5dbdb4e559db1feeb70be63cc
Publikováno v:
Sakarya Üniversitesi Fen Bilimleri Enstitüsü Dergisi, Vol 16, Iss 1 (2012)
In this study, some new derivatives were synthesized of 4-benzoyl-1-(3-nitrophenyl)-5-phenyl-1H-pyrazole-3-carboxylic acid (1) and 4-(ethoxycarbonyl)-1-(3-nitrophenyl)-5-phenyl-1H-pyrazole-3-carboxylic acid (2) that they were pyrazole carboxylic acid
Externí odkaz:
https://doaj.org/article/54b98edc15ec4d4fa644758fb73da4c9
Publikováno v:
Sakarya University Journal of Science, Vol 16, Iss 1 (2012)
Volume: 16, Issue: 1 47-52
Sakarya University Journal of Science
Volume: 16, Issue: 1 47-52
Sakarya University Journal of Science
In this study, some new derivatives were synthesized of 4-benzoyl-1-(3-nitrophenyl)-5-phenyl-1H-pyrazole-3-carboxylic acid (1) and 4-(ethoxycarbonyl)-1-(3-nitrophenyl)-5-phenyl-1H-pyrazole-3-carboxylic acid (2) that they were pyrazole carboxylic acid
Publikováno v:
Journal of the Serbian Chemical Society, Vol 75, Iss 12, Pp 1625-1635 (2010)
WOS: 000286682300002
1-(3-Aminophenyl)-4-benzoyl-5-phenyl-1H-pyrazole-3-carboxylic acid (1) was synthesized according to the literature.(1) 2-(3-Aminophenyl)-2,6-dihydro-3,4-diphenyl-7H-pyrazolo[3,4-d]pyridazin-7-one (5) was obtained by the cycl
1-(3-Aminophenyl)-4-benzoyl-5-phenyl-1H-pyrazole-3-carboxylic acid (1) was synthesized according to the literature.(1) 2-(3-Aminophenyl)-2,6-dihydro-3,4-diphenyl-7H-pyrazolo[3,4-d]pyridazin-7-one (5) was obtained by the cycl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90f0cc777d99bbe7bd5dc37c4f59eb98
https://hdl.handle.net/20.500.12438/5504
https://hdl.handle.net/20.500.12438/5504