Synthesis, antibacterial evaluation, Raman, Crystal Structure and Hirshfeld Surface analysis of a new 3-(4-fluorophenyl)-6-methyl-2-(propylthio)quinazolin-4(3H)-one

[1]  Mohammed H. Geesi.  Synthesis, antibacterial evaluation, Crystal Structure and Hirshfeld surface analysis of a new 2-Benzylsulfanyl-3-(4-fluoro-phenyl)-6-methyl-3H-quinazolin-4-one , 2020 .

[2]  M. E. Moustapha,et al.  Ultrasound-accelerated green synthesis of new quinolin-2-thione derivatives and antimicrobial evaluation against Escherichia coli and Staphylococcus aureus , 2020 .

[3]  Satyendra Mishra.  Quinazolinone and Quinazoline Derivatives: Synthesis and Biological Application , 2019, Quinazolinone and Quinazoline Derivatives.

[4]  Y. Riadi.  UV Light Mediated Palladium-Catalyzed Synthesis of 2-Substituedpyrido[2,3-d]pyrimidines , 2019, Polycyclic Aromatic Compounds.

[5]  Y. Riadi.  UV Light-mediated regioselective methylsulfanyl discrimination via Pd-catalyzed cross-coupling reactions of 2,4-dimethylsulfanylpyrido[2,3-d]pyrimidines , 2019, Journal of Sulfur Chemistry.

[6]  Y. Riadi,et al.  Regioselective palladium-catalyzed Suzuki–Miyaura coupling reaction of 2,4,6-trihalogenopyrido[2,3-d]pyrimidines , 2019, Comptes Rendus Chimie.

[7]  Reza Ghadimi,et al.  Design and synthesis of novel quinazolinone-1,2,3-triazole hybrids as new anti-diabetic agents: In vitro α-glucosidase inhibition, kinetic, and docking study. , 2019, Bioorganic chemistry.

[8]  Mohammed H. Geesi,et al.  Photochemical route for the synthesis of novel 2-monosubstituted pyrido[2,3-d]pyrimidines by palladium-catalyzed cross-coupling reactions , 2018, Chemical Papers.

[9]  R. Al-Salahi,et al.  Screening and evaluation of antioxidant activity of some 1,2,4-triazolo[1,5-a]quinazoline derivatives. , 2018, Future medicinal chemistry.

[10]  R. Al-Salahi,et al.  Molecular Docking and Anticonvulsant Activity of Newly Synthesized Quinazoline Derivatives , 2017, Molecules.

[11]  Shagufta,et al.  An insight into the therapeutic potential of quinazoline derivatives as anticancer agents. , 2017, MedChemComm.

[12]  M. Alshammari,et al.  Novel animal-bone-meal-supported palladium as a green and efficient catalyst for Suzuki coupling reaction in water, under sunlight , 2017 .

[13]  A. Sivakumar,et al.  Design and synthesis of quinazoline carboxylates against Gram-positive, Gram-negative, fungal pathogenic strains, and Mycobacterium tuberculosis , 2014, Journal of pharmacy & bioallied sciences.

[14]  Ankita Rathore,et al.  Synthesis and characterization of quinazoline derivatives: search for hybrid molecule as diuretic and antihypertensive agents , 2014, Journal of enzyme inhibition and medicinal chemistry.

[15]  F. Gao,et al.  Quinazoline derivatives: synthesis and bioactivities , 2013, Chemistry Central Journal.

[16]  J. Leger,et al.  Convenient synthesis of 2,4-disubstituted pyrido[2,3-d]pyrimidines via regioselective palladium-catalyzed reactions , 2012 .

[17]  A. Kadi,et al.  Synthesis, analgesic and anti-inflammatory evaluation of some novel quinazoline derivatives. , 2010, European journal of medicinal chemistry.

[18]  Louis J. Farrugia,et al.  WinGX suite for small-molecule single-crystal crystallography , 1999 .

[19]  Maria Cristina Burla,et al.  SIR97: a new tool for crystal structure determination and refinement , 1999 .

[20]  D. A. Long,et al.  A study of some vibrational band intensities in the pre-resonance Raman spectra of naphthalene, phenazine, pyrazine, cinnoline and quinazoline , 1980 .

[21]  A. Mishra,et al.  A REVIEW ON BIOLOGICAL ACTIVITY OF QUINAZOLINONES , 2012 .

[22]  G. Sheldrick.  A short history of SHELX. , 2008, Acta crystallographica. Section A, Foundations of crystallography.

[23]  G. Socrates,et al.  Infrared and Raman characteristic group frequencies : tables and charts , 2001 .

[24]  E. Simpson.  From the Centers for Disease Control and Prevention. Prevalence of penicillin-resistant Streptococcus pneumoniae--Connecticut, 1992-1993. , 1994, JAMA.