Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Moged A. Berghot"'
Publikováno v:
Journal of Saudi Chemical Society, Vol 20, Iss 2, Pp 151-157 (2016)
A series of thiophene incorporating pyrazolone moieties 5a–f and 6a–c were synthesized via diazo coupling of diazonium salt of 3-substituted-2-amino-4,5,6,7-tetrahydrobenzo[b]thiophenes 1a–c with 3-methyl-1H-pyrazol-5(4H)-one, 3-methyl-1-phenyl
Externí odkaz:
https://doaj.org/article/441879be5eeb43af8304f731f47b967c
Publikováno v:
Journal of Saudi Chemical Society, Vol 20, Iss 2, Pp 165-172 (2016)
Dibenzobarallene was used as a key intermediate for the synthesis of 2-(3-hydroxy-2-naphthoyl)-3,4,4a,5,10,10a-hexahydro-1H-5,10-benzenobenzo[g]phthalazine-1,4-dione (2). The previous compound was coupled with the appropriate diazonium chloride to gi
Externí odkaz:
https://doaj.org/article/3fb08bcccda645b6af5213157cf90fd9
Publikováno v:
Journal of the Serbian Chemical Society, Vol 76, Iss 3, Pp 329-339 (2011)
Dibenzobarallene (1) was utilized as the key intermediate for the synthesis of some new 2-substituted 1,4-dioxo-3,4,4a,5,10,10a-hexahydro-1H-5,10-[1’,2’]-benzenobenzo[g]phthalazine: 2, 5a–d, 8a–c and 10. Condensation of 2 with benzaldehyde or
Externí odkaz:
https://doaj.org/article/2a4bb87332924c33a186246df30fa2ea
Publikováno v:
Journal of the Serbian Chemical Society, Vol 76, Iss 3, Pp 339/S1-339/S4 (2011)
n/a
Externí odkaz:
https://doaj.org/article/08c186262d3f4060b196fe622559c43f
Publikováno v:
Letters in Organic Chemistry. 17:2-23
This review describes the synthesis and reactions of substituted pyrazolo[3,4-b] pyridines as a building block for the synthesis of polyfunctionalized heterocyclic compounds with pharmacological interest.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c2a1524cea66ae10471ef3ddce16b17
https://doi.org/10.2174/1570178616666190411102031
https://doi.org/10.2174/1570178616666190411102031
Publikováno v:
Journal of Heterocyclic Chemistry. 56:2036-2045
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d7b79d5492da19fa67f062bf9c17aa0
https://doi.org/10.1002/jhet.3584
https://doi.org/10.1002/jhet.3584
Autor:
Wafaa S. Hamama, Eman El Baz, Essam H. A. Hanashalshahaby, Moustafa A. Gouda, Moged A. Berghot
Publikováno v:
Organic Communications, Vol 12, Iss 2, Pp 43-100 (2019)
This review presents a systematic and comprehensive survey of the chemical reactivity of 3-acyl(aroyl) coumarins. The target compounds are important intermediates for the synthesis of a variety of synthetically useful and novel heterocyclic systems w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10bfabca48bdf65696f13b744eeb8e5a
https://www.acgpubs.org/doc/2019062315090756-OC-1902-1160.pdf
https://www.acgpubs.org/doc/2019062315090756-OC-1902-1160.pdf
Publikováno v:
Journal of Heterocyclic Chemistry. 55:1935-1941
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::293f3a3a21cd669a1155d16751f5fdef
https://doi.org/10.1002/jhet.3231
https://doi.org/10.1002/jhet.3231
Publikováno v:
Journal of Saudi Chemical Society, Vol 20, Iss 2, Pp 151-157 (2016)
A series of thiophene incorporating pyrazolone moieties 5a–f and 6a–c were synthesized via diazo coupling of diazonium salt of 3-substituted-2-amino-4,5,6,7-tetrahydrobenzo[b]thiophenes 1a–c with 3-methyl-1H-pyrazol-5(4H)-one, 3-methyl-1-phenyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a3cb2a04c9afe14e84ca25038de9e95
http://www.sciencedirect.com/science/article/pii/S1319610312000804
http://www.sciencedirect.com/science/article/pii/S1319610312000804
Publikováno v:
Journal of Heterocyclic Chemistry. 53:1241-1250
One-pot condensation of malononitrile 1, furan-2-carbaldehyde 2, butan-2-one 3, and ammonium acetate in ethanol, followed by cyanoacetylation of the formed nicotinonitrile 4 with 3-(3,5-dimethyl-1H-pyrazol-1-yl)-3-oxopropanenitrile 5 afforded the cya
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0930b64c9f9ff9557ab2525efbd000c
https://doi.org/10.1002/jhet.2414
https://doi.org/10.1002/jhet.2414