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Marei, Mohamed Gaber, Aly, Dalia Mahmoud, Mishrikey, Morcos Michael (1992) A New Synthesis of Pyrazolo[1,5-c]pyrimidines from Acetylenic β-Diketones. Bulletin of the Chemical Society of Japan, 65 (12). 3419-3422 doi:10.1246/bcsj.65.3419

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Reference TypeJournal (article/letter/editorial)
TitleA New Synthesis of Pyrazolo[1,5-c]pyrimidines from Acetylenic β-Diketones
JournalBulletin of the Chemical Society of Japan
AuthorsMarei, Mohamed GaberAuthor
Aly, Dalia MahmoudAuthor
Mishrikey, Morcos MichaelAuthor
Year1992 (December)Volume65
Issue12
PublisherThe Chemical Society of Japan
DOIdoi:10.1246/bcsj.65.3419Search in ResearchGate
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Mindat Ref. ID4497986Long-form Identifiermindat:1:5:4497986:9
GUID0
Full ReferenceMarei, Mohamed Gaber, Aly, Dalia Mahmoud, Mishrikey, Morcos Michael (1992) A New Synthesis of Pyrazolo[1,5-c]pyrimidines from Acetylenic β-Diketones. Bulletin of the Chemical Society of Japan, 65 (12). 3419-3422 doi:10.1246/bcsj.65.3419
Plain TextMarei, Mohamed Gaber, Aly, Dalia Mahmoud, Mishrikey, Morcos Michael (1992) A New Synthesis of Pyrazolo[1,5-c]pyrimidines from Acetylenic β-Diketones. Bulletin of the Chemical Society of Japan, 65 (12). 3419-3422 doi:10.1246/bcsj.65.3419
In(1992, December) Bulletin of the Chemical Society of Japan Vol. 65 (12) The Chemical Society of Japan

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Marei, Mohamed Gaber, Mishrikey, Morcos Michael (1992) A NEW SYNTHESIS OF 6-THIATHIOPHTHENES FROM ACETYLENIC β-DIKETONES. Phosphorus, Sulfur, and Silicon and the Related Elements, 73. 229-234 doi:10.1080/10426509208034447
Marei, Mohamed Gaber, Mishrikey, Morcos Michael (1993) A New Synthesis of 6-Thiathiophthenes From Acetylenic β-Diketones. Phosphorus, Sulfur, and Silicon and the Related Elements, 75. 229-234 doi:10.1080/10426509308037397
Marei, Mohamed Gaber (1993) Preparation and Reactions of 6-Aryl-1,5-dihydro-3-phenyl-4H-pyrazolo[4,3-c]pyridin-4-ones. Bulletin of the Chemical Society of Japan, 66 (4). 1172-1175 doi:10.1246/bcsj.66.1172
Marei, Mohamed Gaber, El-Ghanam, Moneim (1992) Synthesis and Reactions of 1-Heteroaryl-5-phenyl-4-pentyne-1,3-diones. Bulletin of the Chemical Society of Japan, 65 (12). 3509-3511 doi:10.1246/bcsj.65.3509
EL-SAYED EL-KHOLY, I., MISHRIKEY, M. M., MAREI, M. G. (1983) ChemInform Abstract: A New Synthesis of 3(2H)-Furanones from Acetylenic β-Diketones. Chemischer Informationsdienst, 14 (30) doi:10.1002/chin.198330197
Elnagdi, Mohamed Hilmy, Erian, Ayman Wahba (1990) Synthesis of Substituted Azaindenes: Synthesis of New Pyrazolo[1,5-a]pyrimidine Derivatives. Bulletin of the Chemical Society of Japan, 63 (6). 1854-1856 doi:10.1246/bcsj.63.1854
Sadek, Kamal Usef, Selim, Maghraby Aly, El-Maghraby, Mohamed Abdallah (1985) Reactions with heterocyclic amidines: synthesis of several new pyrazolo[1,5-a]pyrimidines and pyrazolo[1,5-c]-as-triazines. Journal of Chemical & Engineering Data, 30 (4) 514-515 doi:10.1021/je00042a048
Marei, Mohamed Gaber, El-Ghanam, Moneim, Salem, Magdi Mohamed (1994) The Synthesis and Cyclodehydration of 4-(3-Aryl-1,3-dioxopropyl)-5-phenyl-1H-1,2,3-triazoles. Novel Substituted Pyrrolo[1,2-c][1,2,3]triazoles. Bulletin of the Chemical Society of Japan, 67 (1). 144-148 doi:10.1246/bcsj.67.144
Elnagdi, Mohamed Hilmy, Zayed, Ezzat Mohamed, Kandeel, Ezzat Mohamed, Fahmy, Sherif Mahmoud (1977) Pyrimidine Derivatives and Related Compounds, VII Synthesis of Some New Pyrazolo [1,5-a] -S-triazines, Pyrazolo [3,4-c] -as-triazines, Pyrazolo [1,5-a] pyrimidines and Pyrazolo [3,4-b] pyrones. Zeitschrift für Naturforschung B, 32. 430-433 doi:10.1515/znb-1977-0416
Badr, Mahmoud Zarif Amin, Aly, Morsy Mohamed, Fahmy, Atiat Mohamed, Mansour, Mansour Esmael Younis (1981) Synthesis of Oxazolidines, Thiazolidines, and 5,6,7,8-Tetrahydro-1H,3H-pyrrolo[1,2-c]oxazole (or thiazole)-1,3-diones from β-Hydroxy- or β-Mercapto-α-amino Acid Esters. Bulletin of the Chemical Society of Japan, 54 (6). 1844-1847 doi:10.1246/bcsj.54.1844
Watarai, Hitoshi, Takano, Mikako, Suzuki, Nobuo (1992) Tautomerization and Dissociation Equilibria of β-Diketones in Microemulsions. Bulletin of the Chemical Society of Japan, 65 (1). 170-174 doi:10.1246/bcsj.65.170
 
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