Zobrazeno 1 - 10
of 42
pro vyhledávání: '"M. M. Girges"'
Publikováno v:
ChemistrySelect. 5:3075-3079
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d86b3d4d18915d600fe071baf11ddae
https://doi.org/10.1002/slct.201904770
https://doi.org/10.1002/slct.201904770
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:
European Journal of Chemistry. 5:595-600
A few new sulphadimidine incorporating thiophene moiety are synthesized. These compounds were assessed by analytical and spectral data. Antioxidant evaluation for the investigated compounds was evaluated by ABTS assay and bleomycin-dependent DNA-dama
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c74a7c2f082b7fdd1a118f528088b039
https://doi.org/10.5155/eurjchem.5.4.595-600.1106
https://doi.org/10.5155/eurjchem.5.4.595-600.1106
Publikováno v:
Journal of Chemical Technology & Biotechnology. 44:299-308
Different heterocyclic Hansa Yellow analogues were synthesized from 3-oxo-N-(pyrazol-4-yl)butanamide for possible use as azodisperse dyes for dyeing polyester fibres. The free energy relationship between the position of absorption of these dyes-λ-an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a31f59db70d6f384ed2cdc970219626
https://doi.org/10.1002/jctb.280440406
https://doi.org/10.1002/jctb.280440406
Publikováno v:
Journal of Chemical Technology & Biotechnology. 55:9-16
The condensation reaction of pyridine-carboxylic acid hydrazides IIa-d with ethyl butanoylacetate was selectively used to synthesize new azo-disperse dyes embodying a pyrazolone moiety with a view to evaluating and comparing their dyeing performance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d14bca0c1c470effe2f74603d24c8a0
https://doi.org/10.1002/jctb.280550103
https://doi.org/10.1002/jctb.280550103
Publikováno v:
Journal of Chemical Technology & Biotechnology. 52:559-570
In a four-step synthesis, a series of N-arylideneamino p-substituted pyridinium salt derivatives were prepared for use as cationic azomethine disperse dyes for polyester and polyacrylonitrile fibres. The effect of different substituents, in both of h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c0db02b55c6aa01b68fb702d7d58fac
https://doi.org/10.1002/jctb.280520413
https://doi.org/10.1002/jctb.280520413
Publikováno v:
Synthetic Communications. 37:1313-1319
A combination of tetrachlorosilane and potassium cyanide (in situ trichlorosilyl cyanide) was found to work efficiently for hydrocyanation of ketones to afford the corresponding cyanohydrins in high yield under mild conditions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b572fff9c19288e4f159b138b0c5988
https://doi.org/10.1080/00397910701226897
https://doi.org/10.1080/00397910701226897
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 179:1577-1593
Benzo[1,2-b:5,4-b′]difuran-2-carbohydrazides 5a, b were reacted with aryl or alkyl isothiocyanates to give the corresponding thiosemicarbazides 6a–h. Cyclization of the substituted thiosemicarbazides with sodium hydroxide led to the formation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::279926c94b99199ea5facd3f3c19dc7c
https://doi.org/10.1080/10426500490464140
https://doi.org/10.1080/10426500490464140
Publikováno v:
Tetrahedron Letters. 38:1071-1074
The successive reactions of some cyclic ketones with aryl methyl ketones mediated by tetrachlorosilane-ethanol, provide an attractive and convenient route to branched functionalized benzenoid compounds. Selective unsymmetrical branched triarylbenzene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::880aabbff8444570965875f984eacdc3
https://doi.org/10.1016/s0040-4039(96)02470-7
https://doi.org/10.1016/s0040-4039(96)02470-7
Publikováno v:
Medicinal Chemistry.
A series of aryl azonaphthoquinones 8a-e were obtained via coupling of the corresponding diazonium salts 7a-c with naphthoquinones 2 or 3 in pyridine. Moreover, treatment of 5 with 6a, b in ethanol containing potassium carbonate afforded the correspo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::42262a5fc6d4cde2ad875da17f45d1ef
https://doi.org/10.4172/2161-0444.1000143
https://doi.org/10.4172/2161-0444.1000143