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Deep insights to explain the mechanism of carbon dot formation at various reaction times using the hydrothermal technique: FT-IR, C-NMR, H-NMR, and UV-visible spectroscopic approaches

RSC advances, 2023-05, Vol.13 (21), p.1434-14349

2023

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Deep insights to explain the mechanism of carbon dot formation at various reaction times using the hydrothermal technique: FT-IR, 13 C-NMR, 1 H-NMR, and UV-visible spectroscopic approaches

RSC advances, 2023-05, Vol.13 (21), p.14340-14349

2023

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Catalytic application of green-synthesized ZnO nanoparticles in the synthesis of 1H-pyrazolo[1,2-a]pyridazine-5,8-diones and evaluation of their anti-cancer properties

New journal of chemistry, 2023-09, Vol.47 (36), p.16809-16818

2023

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Synthesis and Spectroscopic Characterization of Some New Biological Active Azo–Pyrazoline Derivatives

Journal of chemistry, 2012-01, Vol.9 (3), p.1613-1622

2012

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Deep insights to explain the mechanism of carbon dot formation at various reaction times using the hydrothermal technique: FT-IR, 13C-NMR, 1H-NMR, and UV-visible spectroscopic approaches

RSC advances, 2023-05, Vol.13 (21), p.14340-14349

2023

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Crystal structure and Hirshfeld surface analysis of 3-[(1 E )-(4-{4-[( E )-(3-hy-droxy-benzyl-idene)amino]-phen-oxy}phenyl-imino)-meth-yl]phenol

Acta crystallographica. Section E, Crystallographic communications, 2021-03, Vol.77 (Pt 3), p.266-269

2021

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Ultrasound-assisted Synthesis of Some New Curcumin Analogs and Their Corresponding Pyrazoline Derivatives

ARO (Koya), 2017-05, Vol.5 (1), p.30-35

2017

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The structure of 9-(3-bromo-6-chloro-2-hy-droxy-phen-yl)-10-(2-hy-droxy-ethyl)-3,6-diphenyl-3,4,5,6,7,9-hexa-hydro-2H-acridine-1,8-dione

Acta crystallographica. Section E, Crystallographic communications, 2018-09, Vol.74 (Pt 9), p.1218-1221

2018

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Crystal structure of (6E,20E)-3,24-di-fluoro-13,14,28,29-tetra-hydro-5H,22H-tetra-benzo[e,j,p,u][1,4,12,15]tetra-oxa-cyclo-docosine-5,22-dione

Acta crystallographica. Section E, Crystallographic communications, 2017-01, Vol.73 (Pt 1), p.13-16

2017

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Catalytic application of green-synthesized ZnO nanoparticles in the synthesis of 1-pyrazolo[1,2-]pyridazine-5,8-diones and evaluation of their anti-cancer properties

New journal of chemistry, 2023-09, Vol.47 (36), p.1689-16818

2023

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Catalytic application of green-synthesized ZnO nanoparticles in the synthesis of 1 H -pyrazolo[1,2- a ]pyridazine-5,8-diones and evaluation of their anti-cancer properties

New journal of chemistry, 2023-09, Vol.47 (36), p.16809-16818

2023

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Organic soluble nitrogen-doped carbon dots (ONCDs) to reduce the optical band gap of PVC polymer: Breakthrough in polymer composites with improved optical properties

Optical materials, 2024-03, Vol.149, p.115014, Article 115014

2024

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Traditional, one-pot three-component synthesis and anti-bacterial evaluations of some new pyrimidine derivatives

Inorganic chemistry communications, 2024-02, Vol.160, p.111875, Article 111875

2024

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The structure of 9-(3-bromo-6-chloro-2-hy-droxy-phen-yl)-10-(2-hy-droxy-ethyl)-3,6-diphenyl-3,4,5,6,7,9-hexa-hydro-2 H -acridine-1,8-dione

Acta crystallographica. Section E, Crystallographic communications, 2018-09, Vol.74 (Pt 9), p.1218

2018

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( Z )-1-(1,3-Diphenyl-1 H -pyrazol-4-yl)- N -phenylmethanimine N -oxide

IUCrData, 2018-02, Vol.3 (2), p.x180208, Article x180208

2018

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Bis(2-formylphenyl) benzene-1,2-dicarboxylate

IUCrData, 2018-02, Vol.3 (2), p.x180251, Article x180251

2018

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Crystal structure of (6 E ,20 E )-3,24-difluoro-13,14,28,29-tetrahydro-5 H ,22 H -tetrabenzo[ e , j , p , u ][1,4,12,15]tetraoxacyclodocosine-5,22-dione

Acta crystallographica. Section E, Crystallographic communications, 2017-01, Vol.73 (1), p.13-16

2017

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Crystal structure of (6 E ,20 E )-3,24-di-fluoro-13,14,28,29-tetra-hydro-5 H ,22 H -tetra-benzo[ e , j , p , u ][1,4,12,15]tetra-oxa-cyclo-docosine-5,22-dione

Acta crystallographica. Section E, Crystallographic communications, 2017-01, Vol.73 (Pt 1), p.13

2017

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5-{[5-(4-Chlorophenyl)-3-methyl-1 H -pyrazol-1-yl]methyl}-1,3,4-oxadiazole-2(3 H )-thione

IUCrData, 2017-02, Vol.2 (2), p.x170176, Article x170176

2017

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Synthesis and Antimicrobial Ctivity of 3-(4-(4-chlorobenzyloxy)phenyl)-1-phenyl-5-(2-chlorophenyl) Pyrazoline (3) on ＂E. coli＂ in Mice

Asian Journal of Medical Sciences, 2011-08, Vol.3 (4)

2011

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3-Hydroxy-3-(2-oxo-2,3-dihydro-1 H -indol-3-yl)-2,3-dihydro-1 H -indol-2-one

IUCrData, 2017-02, Vol.2 (2), Article x170139

2017

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3-Hydroxy-3-(2-oxo-2,3-dihydro-1H-indol-3-yl)-2,3-dihydro-1H-indol-2-one

IUCrData, 2017-02, Vol.2 (2), p.x170139

2017

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3-[(3,5-Dimethyl-1 H -pyrazol-1-yl)methyl]-4-(4-methylphenyl)-4,5-dihydro-1 H -1,2,4-triazole-5-thione

IUCrData, 2017-02, Vol.2 (2), Article x170153

2017

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4-(3-Methylphenyl)-3-[(3-methyl-5-phenyl-1 H -pyrazol-1-yl)methyl]-4,5-dihydro-1 H -1,2,4-triazole-5-thione

IUCrData, 2017-02, Vol.2 (2), Article x170184

2017

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4-(3-Methylphenyl)-3-[(3-methyl-5-phenyl-1H-pyrazol-1-yl)methyl]-4,5-dihydro-1H-1,2,4-triazole-5-thione

IUCrData, 2017-02, Vol.2 (2), p.x170184

2017

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Deep insights to explain the mechanism of carbon dot formation at various reaction times using the hydrothermal technique: FT-IR, C-NMR, H-NMR, and UV-visible spectroscopic approaches

Deep insights to explain the mechanism of carbon dot formation at various reaction times using the hydrothermal technique: FT-IR, 13 C-NMR, 1 H-NMR, and UV-visible spectroscopic approaches

Catalytic application of green-synthesized ZnO nanoparticles in the synthesis of 1H-pyrazolo[1,2-a]pyridazine-5,8-diones and evaluation of their anti-cancer properties

Synthesis and Spectroscopic Characterization of Some New Biological Active Azo–Pyrazoline Derivatives

Deep insights to explain the mechanism of carbon dot formation at various reaction times using the hydrothermal technique: FT-IR, 13C-NMR, 1H-NMR, and UV-visible spectroscopic approaches

Crystal structure and Hirshfeld surface analysis of 3-[(1 E )-(4-{4-[( E )-(3-hy-droxy-benzyl-idene)amino]-phen-oxy}phenyl-imino)-meth-yl]phenol

Ultrasound-assisted Synthesis of Some New Curcumin Analogs and Their Corresponding Pyrazoline Derivatives

The structure of 9-(3-bromo-6-chloro-2-hy-droxy-phen-yl)-10-(2-hy-droxy-ethyl)-3,6-diphenyl-3,4,5,6,7,9-hexa-hydro-2H-acridine-1,8-dione

Crystal structure of (6E,20E)-3,24-di-fluoro-13,14,28,29-tetra-hydro-5H,22H-tetra-benzo[e,j,p,u][1,4,12,15]tetra-oxa-cyclo-docosine-5,22-dione

Catalytic application of green-synthesized ZnO nanoparticles in the synthesis of 1-pyrazolo[1,2-]pyridazine-5,8-diones and evaluation of their anti-cancer properties

Catalytic application of green-synthesized ZnO nanoparticles in the synthesis of 1 H -pyrazolo[1,2- a ]pyridazine-5,8-diones and evaluation of their anti-cancer properties

Organic soluble nitrogen-doped carbon dots (ONCDs) to reduce the optical band gap of PVC polymer: Breakthrough in polymer composites with improved optical properties

Traditional, one-pot three-component synthesis and anti-bacterial evaluations of some new pyrimidine derivatives

The structure of 9-(3-bromo-6-chloro-2-hy-droxy-phen-yl)-10-(2-hy-droxy-ethyl)-3,6-diphenyl-3,4,5,6,7,9-hexa-hydro-2 H -acridine-1,8-dione

( Z )-1-(1,3-Diphenyl-1 H -pyrazol-4-yl)- N -phenylmethanimine N -oxide

Bis(2-formylphenyl) benzene-1,2-dicarboxylate

Crystal structure of (6 E ,20 E )-3,24-difluoro-13,14,28,29-tetrahydro-5 H ,22 H -tetrabenzo[ e , j , p , u ][1,4,12,15]tetraoxacyclodocosine-5,22-dione

Crystal structure of (6 E ,20 E )-3,24-di-fluoro-13,14,28,29-tetra-hydro-5 H ,22 H -tetra-benzo[ e , j , p , u ][1,4,12,15]tetra-oxa-cyclo-docosine-5,22-dione

5-{[5-(4-Chlorophenyl)-3-methyl-1 H -pyrazol-1-yl]methyl}-1,3,4-oxadiazole-2(3 H )-thione

Synthesis and Antimicrobial Ctivity of 3-(4-(4-chlorobenzyloxy)phenyl)-1-phenyl-5-(2-chlorophenyl) Pyrazoline (3) on ＂E. coli＂ in Mice

3-Hydroxy-3-(2-oxo-2,3-dihydro-1 H -indol-3-yl)-2,3-dihydro-1 H -indol-2-one

3-Hydroxy-3-(2-oxo-2,3-dihydro-1H-indol-3-yl)-2,3-dihydro-1H-indol-2-one

3-[(3,5-Dimethyl-1 H -pyrazol-1-yl)methyl]-4-(4-methylphenyl)-4,5-dihydro-1 H -1,2,4-triazole-5-thione

4-(3-Methylphenyl)-3-[(3-methyl-5-phenyl-1 H -pyrazol-1-yl)methyl]-4,5-dihydro-1 H -1,2,4-triazole-5-thione

4-(3-Methylphenyl)-3-[(3-methyl-5-phenyl-1H-pyrazol-1-yl)methyl]-4,5-dihydro-1H-1,2,4-triazole-5-thione

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