Heterocyclic Synthesis via Enaminones: Synthesis and Molecular Docking Studies of Some Novel Heterocyclic Compounds Containing Sulfonamide Moiety

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International Journal of Organic Chemistry

ISSN Print: 2161-4687
ISSN Online: 2161-4695
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"Heterocyclic Synthesis via Enaminones: Synthesis and Molecular Docking Studies of Some Novel Heterocyclic Compounds Containing Sulfonamide Moiety"
written by Ahmed Abd El-Hameed Hassan,
published by International Journal of Organic Chemistry, Vol.4 No.1, 2014

has been cited by the following article(s):

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[2]	Visible light photoredox catalysis for the synthesis of new chromophores as co-sensitizers with benchmark N719 for highly efficient DSSCs Optical Materials, 2023 DOI:10.1016/j.optmat.2023.114454

[3]	Advances in Heterocyclic Chemistry, 2021 DOI:10.1016/bs.aihch.2021.01.002

[4]	Synthesis, antimicrobial and antiproliferative activities, molecular docking, and computational studies of novel heterocycles Journal of the Iranian Chemical Society, 2021 DOI:10.1007/s13738-021-02251-7

[5]	Advances in Heterocyclic Chemistry, 2021 DOI:10.1016/bs.aihch.2021.01.002

[6]	Chemoselective Synthesis and Evaluation of β-Oxovinylarsines as an Arsenic Synthetic Precursor Organometallics, 2020 DOI:10.1021/acs.organomet.9b00587

[7]	Chemoselective Synthesis and Evaluation of β-Oxovinylarsines as an Arsenic Synthetic Precursor Organometallics, 2020 DOI:10.1021/acs.organomet.9b00587

[8]	Enaminone-Derived Pyrazoles with Antimicrobial Activity Journal of Chemistry, 2019 DOI:10.1155/2019/2467970

[9]	Synthesis of a novel functionalized tricyclic pyrimidine-fused 1,5-benzodiazepine library Tetrahedron, 2017 DOI:10.1016/j.tet.2017.03.079

[10]	Synthesis of Biodegradable Pyrazole, Pyran, Pyrrole, Pyrimidine and Chromene Derivatives having Medical and Surface Activities Journal of Surfactants and Detergents, 2016 DOI:10.1007/s11743-016-1881-0

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[12]	Mass spectral study of the occurrence of tautomeric forms of selected enaminones International Journal of Mass Spectrometry, 2015 DOI:10.1016/j.ijms.2014.12.010

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