Results 1 to 10 of about 881 (119)

Protease inhibition, in vitro antibacterial and IFD/MM-GBSA studies of ciprofloxacin-based acetanilides. [PDF]

open access: yesPLoS ONE, 2023
In this study, we have investigated ciprofloxacin-based acetanilides for their in-vitro inhibitory study against gram +ve, -ve bacteria and serine protease activity.
Rabia Akhtar   +6 more
doaj   +2 more sources

Benzo[d]oxazoles from Anilides by N-Deprotonation–O-SNAr Cyclization [PDF]

open access: yesMolecules
A synthesis of benzo[d]oxazoles by an N-deprotonation–O-SNAr cyclization sequence from anilide precursors is reported. Anilides derived from 2-fluorobenzaldehydes, activated toward SNAr ring closure by C5 electron-withdrawing groups, were prepared and ...
Nash E. Nevels   +2 more
doaj   +2 more sources

A challenging redox neutral Cp*Co(III)-catalysed alkylation of acetanilides with 3-buten-2-one: synthesis and key insights into the mechanism through DFT calculations [PDF]

open access: yesBeilstein Journal of Organic Chemistry, 2018
Traditional, established palladium cross-coupling procedures are widely applied in complex molecule synthesis; however, there is a significant disadvantage in the requirement for pre-functionalised substrates (commonly halides/triflates).
Andrew Kenny   +5 more
doaj   +2 more sources

Direct additive-free N-formylation and N-acylation of anilines and synthesis of urea derivatives using green, efficient, and reusable deep eutectic solvent ([ChCl][ZnCl2]2) [PDF]

open access: yesScientific Reports
In the current report, we introduce a simple, mild efficient and green protocol for N-formylation and N-acetylation of anilines using formamide, formic acid, and acetic acid as inexpensive, nontoxic, and easily available starting materials just with ...
Fatemeh Abbasi, Ali Reza Sardarian
doaj   +2 more sources

Coordination compounds of Cu(II) with some substituted 2-(3,5-dimethyl-pyrazol-1-yl)-methyl-acetanilides as ligands [PDF]

open access: yesJournal of the Serbian Chemical Society, 2007
New complexes of Cu(II) with some substituted 2-(3,5-dimethyl-pyrazol-1-yl)-methyl-acetanilides (L) hae been synthesized. The complex compounds, CuL4X2 (where X- = Cl,Br, CH3COO) were characterized by elemental analysis, as well as IR, UV-VIS, EPR ...
Zalaru Christina   +5 more
doaj   +3 more sources

Synthesis and Antibacterial Activity of Thymyl Ethers

open access: yesChemistry Proceedings, 2021
In this paper, we report herein a simple and efficient synthesis method of thymyl ethers for structural modifications of natural products such as monoterpenoids and studies of ether derivatives of thymol in biological importance.
Jagdish U. Patil   +2 more
doaj   +1 more source

N-acetylation of 2-aminobenzothiazoles with Acetic Acid for Evaluation of Antifungal Activity and In Silico Analysis

open access: yesJournal of Molecular Docking, 2021
Acetamides (S30A1 and S30) were synthesized from benzo[d]thiazol-2-amine and 6-nitrobenzo[d]thiazol-2-amine by direct use of acetic acid instead of acetylating agents.
Sukumar Bepary   +4 more
doaj   +1 more source

2,2-Dichloro-N-(3,5-dimethylphenyl)acetamide

open access: yesActa Crystallographica Section E, 2008
The structure of the title compound, C10H11Cl2NO, resembles those of 2,2-dichloro-N-phenylacetamide, 2,2-dichloro-N-(2-methylphenyl)acetamide, 2,2-dichloro-N-(3-methylphenyl)acetamide, 2,2-dichloro-N-(4-methylphenyl)acetamide, N-(3,5-dimethylphenyl ...
B. Thimme Gowda   +4 more
doaj   +1 more source

Design and Synthesis of New Hydantoin Acetanilide Derivatives as Anti-NSCLC Targeting EGFRL858R/T790M Mutations

open access: yesPharmaceuticals, 2022
Epidermal Growth Factor Receptor (EGFR), its wild type and mutations L858R/T790M, is overexpressed in non-small cell lung cancer (NSCLC) patients and is considered an inevitable oncology target.
Moamen A. Hassanin   +5 more
doaj   +1 more source

Palladium-catalyzed ortho-halogenations of acetanilides with N-halosuccinimides via direct sp2 C–H bond activation in ball mills

open access: yesBeilstein Journal of Organic Chemistry, 2018
A solvent-free palladium-catalyzed ortho-iodination of acetanilides using N-iodosuccinimide as the iodine source has been developed under ball-milling conditions. This present method avoids the use of hazardous organic solvents, high reaction temperature,
Zi Liu, Hui Xu, Guan-Wu Wang
doaj   +1 more source

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