M. Z. A. BADR
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View article: Synthesis and biological study of some new naphtho[2,1-<i>b</i>]furan and related heterocyclic systems
Synthesis and biological study of some new naphtho[2,1-<i>b</i>]furan and related heterocyclic systems Open
In the reaction of 1-cyano-2-naphthol (4) or its sodium salt with different alkylating agent, the O-alkylated derivatives (5a–d) were produced which underwent ring closure reactions using sodium ethoxide solution to give aminonaphtho [2,1-…
View article: Synthesis of New Triazolo[4',5':2,3]-triazino[5,6-b]quinoxalines
Synthesis of New Triazolo[4',5':2,3]-triazino[5,6-b]quinoxalines Open
Reaction of triazino[5,6-b]-3(4H)-quinoxalin one 2 with and/or pocl3 gave triazinoquinoxalin-3-thione 3 and/or the corresponding 3-chloro derivative 7. Treatment of 3 with alkvl (aralkyl) halides gave the corresponding 3-thioalkyl substitu…
View article: Chemistry and Cyclisation Reactions of Pyrimidothienoquinoxaline Derivatives. Part-IV
Chemistry and Cyclisation Reactions of Pyrimidothienoquinoxaline Derivatives. Part-IV Open
Chemistry Department, Faculty of Science, Assiut University, Assiut, Egypt Manuscript received 4 April 1994, revised 26 May 1995, accepted 20 June 1995 The pyrimidothienoquinoxaline (2a; R = OH), derived from 1 and formamide, is thionated …
View article: Preparation of New Azole and Pyrimidine Derivatives
Preparation of New Azole and Pyrimidine Derivatives Open
Chemistry Department, Faculty of Science, Aswan, Egypt Organic Chemistry Division, Duisburg University, Duisburg, Germany Manuscript received 9 June 1992, revised I February 1994, accepted 8 February 1994 Preparation of New Azole and Pyrim…
View article: Novel Synthesis of Furo[2,3-<i>b</i>]indole Derivatives
Novel Synthesis of Furo[2,3-<i>b</i>]indole Derivatives Open
Isatin reacted with diethyl 3-amino-2-cyano-2-pentenedioate in ethanol and in presence of Et3N to give 3-(1-amino-2-cyano-2-ethoxycarbonylethenyl-2H-furo[2,3-b]indol-2-one. The reaction of (2-oxo-3-indolinylidene)malononitrile (3a) with th…
View article: Reaction of Quinoxaline Derivatives with Nucleophilic Reagents
Reaction of Quinoxaline Derivatives with Nucleophilic Reagents Open
2-Chloro-3-methylquinoxaline reacts with aromatic amines in basic medium forming 2-arylamino-3-methylquinoxalines, also it reacts with mercaptoacetic acid. The 3-methyl-2(1H)-quinoxalinone condenses with aromatic aldehydes forming the corr…
View article: Studies on Synthesis of 6-Bromo-2,3-disubstituted 4(3<i>H</i>)-Quinazolinones and Their Thiones
Studies on Synthesis of 6-Bromo-2,3-disubstituted 4(3<i>H</i>)-Quinazolinones and Their Thiones Open
Synthesis of some 2,3-disubstituted 6-bromo-4(3H)-quinazolinones is described. Treatment of some 4-quinazolinones with phosphorus pentasulfide gave the corresponding 4-quinazolinethiones. The reaction of 6-bromo-2-methyl-3,1-benzoxazin-4-o…
View article: Molecular Rearrangements, XV Photolysis and Thermolysis of N-<sub>a</sub>- and ß-Phenethyl Toluidines
Molecular Rearrangements, XV Photolysis and Thermolysis of N-<sub>a</sub>- and ß-Phenethyl Toluidines Open
Direct irradiation of each of N-a- and /3-phenethyl toluidine in carbon tetrachloride solution leads t o homolysis of the phenethyl-nitrogen bond forming phenethyl and arylamino free radicals. The fates of such radicals are discussed in te…
View article: Molecular Rearrangements. VII. <i>N</i>-Alkylarylamines (III). Thermal Rearrangement of Secondary Arylamines
Molecular Rearrangements. VII. <i>N</i>-Alkylarylamines (III). Thermal Rearrangement of Secondary Arylamines Open
Heating of N-benzyl-o- and p-toluidines resulted in migration of the benzyl group to the corresponding toluidine nucleus. The pyrolysis of N-benzyl-o-toluidine produced ammonia, toluene, bibenzyl, trans-stilbene, o-toluidine together with …
View article: Molecular Rearrangements. Part IV. Aryl (Alkyl) Amines (1), Thermal Rearrangement of <i>N</i>-Benzyl-<i>N</i>-Methylaniline
Molecular Rearrangements. Part IV. Aryl (Alkyl) Amines (1), Thermal Rearrangement of <i>N</i>-Benzyl-<i>N</i>-Methylaniline Open
Heating N-benzyl-N-methylaniline under reflux or heating at ∼315° in sealed tubes, in the absence of any promotor for 100 h, resulted in its rearrangement, producing methylamine, diphenylmethane, and dibenzyl together with o-toluidine and …