International Journal of Organic Chemistry

International Journal of Organic Chemistry

ISSN Print: 2161-4687
ISSN Online: 2161-4695
www.scirp.org/journal/ijoc
E-mail: ijoc@scirp.org
"Highly Efficient Synthesis of Novel Fluorine Bearing Quinoline-4-carboxylic Acid and the Related Compounds as Amylolytic Agents"
written by Mohammed S. T. Makki, Dina A. Bakhotmah, Reda M. Abdel-Rahman,
published by International Journal of Organic Chemistry, Vol.2 No.1, 2012
has been cited by the following article(s):
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[2] Domino Reaction of Isatins with α‐Oxoketene‐N,S‐acetals: An Efficient Synthesis of Pyrrolo[3,4‐c]quinoline‐1,3‐diones and 2,3‐Dihydro‐1H‐pyrrolo[3,4‐c] …
Asian Journal of Organic …, 2021
[3] Synthesis and reactivity of fluorinated heterocycles
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[4] New quinoline carboxylic acid derivatives in the synthesis of biologically active substances
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[5] Synthesis, Characterization, and Antileishmanial Activity of Certain Quinoline-4-carboxylic Acids
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[6] Recent Advances in Catalytic Asymmetric Intermolecular Oxidation of Alkyne
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[10] Divergent synthesis of N-heterocycles via controllable cyclization of azido-diynes catalyzed by copper and gold
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[11] Spectroscopic properties, anti-colon cancer, antimicrobial and molecular docking studies of silver (I), manganese (II), cobalt (II) and nickel (II) complexes for 2 …
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[12] Synthesis and biological evaluation of fluorine substituted pyrazolo [4, 3-e][1, 2, 4] triazines as purine analogues
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[13] ИЗОМЕРНЫЕ ФЕНИЛЕНДИАМИНЫ В ТРЕХКОМПОНЕТНОЙ ЦИКЛОКОНДЕНСАЦИИ С АРОМАТИЧЕСКИМИ АЛЬДЕГИДАМИ И ЦИКЛОПЕНТАДИЕНОМ
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[14] Synthesis of Novel α-Amino Acids Bearing 1, 2, 4-Triazinone and Steroidal Moieties as Enzymatic Affects (Cellobaiase Activity)–Part II
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[15] Convenient one-step synthesis of pyrrolo [3, 4-c] quinolin-1-ones via TMSCl-catalyzed cascade reactions of isatins and β-enamino ketones
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[16] ИЗОМЕРНЫЕ ФЕНИЛЕНДИАМИНЫ В ТРЕХКОМПОНЕТНОЙ ЦИКЛОКОНДЕНСАЦИИ С АРОМАТИЧЕСКИМИ АЛЬДЕГИДАМИ И …
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[17] Synthesis of New Fluorinated 1, 2, 4-Triazino [3, 4-b][1, 3, 4] thiadiazolones as Antiviral Probes-Part II-Reactivities of Fluorinated 3-Aminophenyl-1, 2, 4 …
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[18] Synthesis of some new fluorine substituted thiobarbituric acid derivatives as anti HIV1 and cyclin-dependent kinase 2 (CDK2) for cell tumor division: Part I
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[19] Synthesis of new 6-Spiro (Testosteron-3′-yl)-Hexahydro-3-Thioxo-1, 2, 3-Triazin-5-Ones and Related Derivatives as Affecting Enzymatic Agents
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[20] Synthesis of New Fluorinated 1, 2, 4-Triazino [3, 4-b][1, 3, 4] thiadiazolones as Antiviral Probes-Part II-Reactivities of Fluorinated 3-Aminophenyl-1, 2, 4-triazinothiadiazolone
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[21] Microwave-Assisted Synthesis of Diverse Pyrrolo [3, 4-c] quinoline-1, 3-diones and Their Antibacterial Activities
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[22] Synthesis of 4‐Aryl‐8‐fluoro‐3a, 4, 5, 9b‐tetrahydro‐3H‐cyclopenta [c] quinolines and Their Ozonides
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[23] Synthesis of New Fluorine/Phosphorus Substituted 6-(2’-Amino phenyl)-3-thioxo-1, 2, 4-triazin-5 (2H, 4H) One and Their Related Alkylated Systems as Molluscicidal Agent as against the Snails Responsible for Bilharziasis Diseases
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[24] Synthesis of Some New Fluorine Substituted Thiobarbituricacid Derivatives as Anti HIV1 and Cyclin-Dependent Kinase 2 (CDK2) for Celltumer Division-Part II
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[25] Synthesis of New Fluorine/Phosphorus Substituted 6-(2'-Amino phenyl)-3-thioxo-1, 2, 4-triazin-5 (2H, 4H) One and Their Related Alkylated Systems as Molluscicidal …
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[26] Microwave-Assisted Synthesis of Diverse Pyrrolo[3,4-c]quinoline-1,3-diones and Their Antibacterial Activities
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[27] Synthesis of 4‐Aryl‐8‐fluoro‐3a,4,5,9b‐tetrahydro‐3H‐cyclopenta[c]quinolines and Their Ozonides
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[28] Synthesis of New Fluorine/Phosphorus Substituted 6-(2'-Amino phenyl)-3-thioxo-1, 2, 4-triazin-5 (2H, 4H) One and Their Related Alkylated Systems as …
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[29] Efficient one-step synthesis of pyrrolo [3, 4-c] quinoline-1, 3-dione derivatives by organocatalytic cascade reactions of isatins and β-ketoamides
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[30] Designing and synthesis of new fluorine substituted pyrimidine-thion-5-carbonitriles and the related derivatives as photochemical probe agents for inhibition of …
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[31] Designing and synthesis of new fluorine substituted pyrimidine-thion-5-carbonitriles and the related derivatives as photochemical probe agents for inhibition of vitiligo disease
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