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Synthesis, biological evaluation and DFT calculation of novel pyrazole and pyrimidine derivatives
The utility of the enaminonitriles 3a and 3b for the synthesis of the pyrazole derivatives 5a, b,
7a, b, diaminopyrimidine derivatives 9, 11, pyrazolo [1, 5-a] pyrimidines 12, 15, triazolo [4, 3 …
7a, b, diaminopyrimidine derivatives 9, 11, pyrazolo [1, 5-a] pyrimidines 12, 15, triazolo [4, 3 …
[HTML][HTML] Novel hybrid thiazoles, bis-thiazoles linked to azo-sulfamethoxazole: Synthesis, docking, and antimicrobial activity
The reaction of sulfamethoxazolehydrazonoyl chloride with thiosemicarbazones, bis-
thiosemicarbazones, or 4-amino-3-mercapto-1, 2, 4-triazole in dioxane in the presence of …
thiosemicarbazones, or 4-amino-3-mercapto-1, 2, 4-triazole in dioxane in the presence of …
Utility of 2-Chloro-N-arylacetamide and 1,1′-(Piperazine-1,4-diyl)bis(2-chloroethanone) as Versatile Precursors for Novel Mono- and Bis[thienopyridines]
A series of novel thieno [2, 3-b] pyridines linked to N-aryl carboxamides or
(carbonylphenoxy)-N-(aryl) acetamides, as well as bis (thieno [2, 3-b] pyridines) linked to …
(carbonylphenoxy)-N-(aryl) acetamides, as well as bis (thieno [2, 3-b] pyridines) linked to …
Medicinal chemistry of pyrazolopyrimidine scaffolds substituted with different heterocyclic nuclei
Background: Medicinal chemistry of pyrazolopyrimidine scaffolds substituted with different
heterocyclic nuclei has attracted great attention due to their wide range of biological …
heterocyclic nuclei has attracted great attention due to their wide range of biological …
[HTML][HTML] Synthesis of novel star-shaped molecules based on a pentaerythritol core linked to different heterocyclic systems
Synthesis of analogs of known active compounds is the most often employed strategy for
producing important compounds. The Hantzsch reaction was employed to create new star …
producing important compounds. The Hantzsch reaction was employed to create new star …
Synthesis and DFT calculations of aza-Michael adducts obtained from degradation poly (methyl methacrylate) plastic wastes
Aza-Michael adducts are obtained in excellent yields by the conjugate addition of
nucleophilic reagents with α, β-unsaturated substrates such as methyl methacrylate (MMA) …
nucleophilic reagents with α, β-unsaturated substrates such as methyl methacrylate (MMA) …
[PDF][PDF] Novel bis ([triazolo [3, 4-b] thiadiazoles and bis ([triazolo [3, 4-b][thiadiazines) with antioxidant activity
AHM Elwahy, ARS Ginidi, MR Shaaban… - Arkivoc, 2024 - pdfs.semanticscholar.org
A novel bis-triazole was synthesized in this context, and its potential usage as a flexible
precursor for new bistriazolothiadiazines and bis-triazolothiadiazoles with antioxidant …
precursor for new bistriazolothiadiazines and bis-triazolothiadiazoles with antioxidant …
Regioselective synthesis and DFT study of novel fused heterocyclic utilizing Thermal heating and Microwave Irradiation
Regioselective facile synthesis of innovative heterocycles from the reaction of 2-cyano-N-
cyclohexylacetamide (3) with N, N-dimethylformamide dimethylacetal (DMF-DMA) to afford …
cyclohexylacetamide (3) with N, N-dimethylformamide dimethylacetal (DMF-DMA) to afford …
[PDF][PDF] Microwave assisted regioselective synthesis and biological evaluation of pyrano [2, 3-c] pyridine derivatives utilizing DMAP as a catalyst
AM Fahim - Online J. Biol. Sci., 2017 - academia.edu
Regioselective facile production of pyrano [2, 3-c] pyridine through multicomponent reaction
of aromatic aldehydes, ethyl cyano acetate or malononitrile and CH activated compound of 3 …
of aromatic aldehydes, ethyl cyano acetate or malononitrile and CH activated compound of 3 …
Decoding the reaction mechanism of the cyclocondensation of ethyl acetate2‐oxo‐2‐(4‐oxo‐4H‐pyrido [1.2‐a] pyrimidin‐3‐yl) polyazaheterocycle and …
MB Maraf, AA Idrice… - Journal of …, 2022 - Wiley Online Library
We investigated the flow of electron density along the cyclocondensation reaction between
ethyl acetate 2‐oxo‐2‐(4‐oxo‐4 H‐pyrido [1.2‐a] pyrimidin‐3‐yl) polyazaheterocycle (1) …
ethyl acetate 2‐oxo‐2‐(4‐oxo‐4 H‐pyrido [1.2‐a] pyrimidin‐3‐yl) polyazaheterocycle (1) …