Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Sayed A S, Mousa"'
Autor:
Sanaa A. Ahmed, Moumen S. Kamel, Moustafa O. Aboelez, Xiang Ma, Ahmed A. Al-Karmalawy, Sayed A. S. Mousa, Elders Kh. Shokr, H. Abdel-Ghany, Amany Belal, Mohamed A. El Hamd, Zafer S. Al Shehri, Mahmoud Abd El Aleem Ali Ali El-Remaily
Publikováno v:
ACS Omega. 7:45535-45544
Autor:
Ahmed H. H. Hussien, Mohamed I. H. El‐Qaliei, Sayed A. S. Mousa, Ahmed A. Atalla, Ahmed Khodairy
Publikováno v:
Journal of Heterocyclic Chemistry. 59:1551-1560
Autor:
Sanaa A, Ahmed, Moumen S, Kamel, Moustafa O, Aboelez, Xiang, Ma, Ahmed A, Al-Karmalawy, Sayed A S, Mousa, Elders Kh, Shokr, H, Abdel-Ghany, Amany, Belal, Mohamed A, El Hamd, Zafer S, Al Shehri, Mahmoud Abd, El Aleem Ali Ali El-Remaily
Publikováno v:
ACS omega. 7(49)
Microwave-assisted synthesis and spectral analysis of certain novel derivatives of 3,4-diaminothieno[2,3
Publikováno v:
OALib. :1-9
The Hantzsch amide derivatives 1 are prepared by reaction of a mixture of two moles of benzoylacetone, aqueous ammonia and aromatic aldehydes. Also, the reaction of benzoylacetone with a mixture of urea or thiourea and aromatic aldehydes afforded pyr
Publikováno v:
International Journal of Organic Chemistry. :319-330
Reaction of acetylacetone with 1 mole of dimethylformamide dimethyl acetal (DMFDMA) affords enamine 2a which reacts with cyanothioacetamide to give pyridinethione 3a. Pyridinethione 3a reacts with methyl iodide, halogenated compounds, aromatic aldehy
Publikováno v:
International Journal of Organic Chemistry. :207-214
Reaction of N,N’-dimethylformamide dimethyl acetal (DMFDMA) with malononitrile dimer 8 (1:1) mole afforded 9 while, this reaction when carried out in (2:1) mole to give amidine 11 which can be used for the preparation of pyrimidine 13, amidine 14 a
Publikováno v:
Journal of Heterocyclic Chemistry. 46:801-827
This review focuses on the use of dimethylformamide dimethyl acetal in the preparation of heterocyclic compounds via formylation of active methylene groups, methyl groups to give enamines, and formylation of amino groups to give amidines. These compo
Publikováno v:
Synthetic Communications. 38:376-382
Reactions of chloroacetamides (5) with N,N‐dimethylformamide dimethyl acetal gave 1,4‐diaryl‐piperazine‐2,5‐diones 11a–e in good yield, rather than 1,5‐diaryl‐3,7‐dimethoxy‐1H,5H‐[1,5]diazocine‐2,6‐diones (9a–e).
Publikováno v:
Journal of Sulfur Chemistry. 27:293-305
β-aminocrotononitrile (1) reacted with either cyanothioacetamide to give (3) or malononitrile to afford an anion (5). Pyridine-2(1H)-thione (4) was obtained by boiling of (3) in ethanol and Et 3N or treatment of (5) with H 2S, respectively. The reac
ChemInform Abstract: Dimethylformamide Dimethyl Acetal as a Building Block in Heterocyclic Synthesis
Publikováno v:
ChemInform. 41
This review focuses on the use of dimethylformamide dimethyl acetal in the preparation of heterocyclic compounds via formylation of active methylene groups, methyl groups to give enamines, and formylation of amino groups to give amidines. These compo