Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Sadek Elsayed Abdou"'
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 88:217-224
The reactions of hydrazidoyl halides with N-phenylcyanothioacetamide and α-cyanothioacetamide gave unexpected hydrazidoyl sulfides, thiadiazolines and thiazole derivatives. The structures of these products were confirmed by elemental analyses and sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c1e80cf216f4543aab0ad2690e0101c
https://doi.org/10.1080/10426509408036924
https://doi.org/10.1080/10426509408036924
Publikováno v:
Modern Applied Science. 5
Several new visnaginone ethers were prepared and their thiosemicarbazone derivatives are synthesized. The behavior of the thiosemicarbazones in methanolic sodium methoxide and hydrochloric acid is discussed. Structures were established on the bases o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::295ba2dfb57a7d8822c3b59baca72c71
https://doi.org/10.5539/mas.v5n5p140
https://doi.org/10.5539/mas.v5n5p140
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b218701a26170574348d8897aa9bc37
https://doi.org/10.1002/chin.199502100
https://doi.org/10.1002/chin.199502100
Publikováno v:
Archives of Pharmacal Research. 15:317-321
Furoylhydroximoyl chloride3 reacted with 2-aminopyridine, 2-aminopyrimidine,O-aminophenol,O-phenylenediamine and aminothiophenol to afford imidazo[1,2-a]pyridine6, imidazo[1,2-a]pyrimidine8, benzoxadiazine10, nitrosobenzopyrazine13a and nitrosobenzot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::698a9f57f7f954910d83b6bf39025ab3
https://doi.org/10.1007/bf02974105
https://doi.org/10.1007/bf02974105
Publikováno v:
Archiv der Pharmazie. 316:564-569
Several new pyridine derivatives were synthesised by the reaction of 2-amino-1,1,3-tricyanopropene (2) with acetylacetone and salicyl aldehyde and treatment of the products with active methylene reagents and hydrazines. The structures of the isolated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d807393f69f83b867692d14a1f61edf
https://doi.org/10.1002/ardp.19833160616
https://doi.org/10.1002/ardp.19833160616
Publikováno v:
Monatshefte für Chemie - Chemical Monthly. 113:985-991
Several new benzopyran and benzopyranopyridine derivatives were synthesized via condensation of 2-amino-1,1,3-tricyanopropene (1) and diethyl 2-amino-1-cyanopropene-1,3-dicarboxylate (2) with salicylaldehyde and treatment of the resulted products wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e7e7d0113a7a697e2b9f0eca789f244
https://doi.org/10.1007/bf00799239
https://doi.org/10.1007/bf00799239
Publikováno v:
Synthesis. 1982:502-504
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::323089b9c62e8eecf3e2ccf980686ada
https://doi.org/10.1055/s-1982-29857
https://doi.org/10.1055/s-1982-29857
Publikováno v:
Bulletin of the Chemical Society of Japan. 48:2200-2202
Xanthenyl and thioxanthenyl chlorides (1) were added to 1,1-bis-(p-alkoxyphenyl)-2-substituted-ethylenes (2) to give 1,1-bis-(p-alkoxyphenyl)-2-substituted-2-[xanthen(or thioxanthen)-9-yl]ethylenes...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32c90d22fc9e1f310236752fb907f624
https://doi.org/10.1246/bcsj.48.2200
https://doi.org/10.1246/bcsj.48.2200
Publikováno v:
Chemischer Informationsdienst. 17
New furylpyrrolopyrazole derivatives were synthesised by reacting N-arylmaleimides with furfural phenylhydrazone. The products are to be tested for their biological activities and for chemical transformations. Umsetzungen mit Maleinimiden: Synthese e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba4c44cab8b32bc199127bf02a94b90a
https://doi.org/10.1002/chin.198612234
https://doi.org/10.1002/chin.198612234
Publikováno v:
Chemischer Informationsdienst. 13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4fb8710262a2e0fd782ffa69b9e83e48
https://doi.org/10.1002/chin.198240172
https://doi.org/10.1002/chin.198240172