نتایج جستجو برای: arylidene

تعداد نتایج: 334  

Journal: :Acta poloniae pharmaceutica 2009
Neeraj K Fuloria Vijender Singh Mohammad Shahar Yarb Mohammad Ali

Methyl 3-phenylpropanoate (1), after hydrazination into 3-phenylpropanehydrazide (2), was converted into N-arylidene-3-phenylpropane hydrazides (3a-e), which on cyclization with thioglycolic acid yielded N-(4-oxo-2-arylthiazolidin-3-yl)-3-phenylpropanamides (4a-e). All the proposed structures of newly synthesized compounds were in full agreement with the spectral data. Due to para substitution,...

Journal: :Angewandte Chemie 2021

Efforts to generate organomanganese reagents under ball-milling conditions have led the serendipitous discovery that manganese metal can mediate reductive dimerization of arylidene malonates. The newly uncovered process has been optimized and its mechanism explored using CV measurements, radical trapping experiments, EPR spectroscopy, solution control reactions. This unique reactivity also be t...

Journal: :Russian Journal of Bioorganic Chemistry 2022

Abstract— We report two new analogs of the N871b fluorogen that contain CycloOctaTetraene. have studied photostability fluorescent complexes FAST protein with compounds by confocal microscopy when staining living HeLa Kyoto cells. One exhibits a higher in complex than previously published fluorogen. The results indicate cyclooctatetraene is highly promising compound for modification dyes based ...

Journal: :Molecules 2012
Haider Behbehani Hamada Mohamed Ibrahim

The 4-thiazolidinones 3a-d were used as a key intermediates for the synthesis of 2-arylimino-5-arylidene-4-thiazolidinones derivatives 7a–p via nucleophilic addition reactions with the arylidene malononitrile. Moreover the 4-thiazolidinones 3a and 3c condensed with the DMF-DMA to form the corresponding enamines 8 and 9 depending on the reaction conditions. Otherwise the 4-thiazolidinone 3b reac...

Journal: :Journal of medicinal chemistry 2011
Tamás Kálai M Lakshmi Kuppusamy Mária Balog Karuppaiyah Selvendiran Brian K Rivera Periannan Kuppusamy Kálmán Hideg

A series of 3,5-bis(arylidene)-4-piperidone (DAP) compounds are considered as synthetic analogues of curcumin for anticancer properties. We performed structure-activity relationship studies by synthesizing a number of DAPs N-alkylated or acylated with nitroxides or their amine precursors as potent antioxidant moieties. Both subtituents on arylidene rings and on piperidone nitrogen (five- or six...

1-[4-(2-Alkylaminoethoxy)phenylcarbonyl]-3,5-bis(arylidene)-4-piperidones are a novel class of potent cytotoxic agents. These compounds demonstrate low micromolar to submicromolar IC50 values against human Molt 4/C8 and CEM T-lymphocytes and murine leukemia L1210 cells. In this study, a comparative QSAR investigation was performed on a series of 3,5-bis(arylidene)-4-piperidones using different ...

PVC/NiFe2O4/Fe2O3 compositewas successfully synthesized and characterized by Fourier transform infrared spectroscopy (FT-IR), X-ray powder diffraction (XRD), and scanning electron microscopy (SEM). Also, the catalytic activity of PVC/NiFe2O4/Fe2O3 has been considered in the synthesis of two arylidene barbitu...

Journal: :Molecules 2013
Oana Maria Dragostin Florentina Lupascu Cornelia Vasile Mihai Mares Valentin Nastasa Ramona Florina Moraru Dragos Pieptu Lenuta Profire

New series of N-(arylidene)hydrazinoacetyl sulfonamides 4a1-6, 4b1-6 and N-(4-aryl-3-chloro-2-oxoazetidin-1-yl)aminoacetyl sulfonamides 5a1-6, 5b1-6 were synthesized. The structures of the new derivatives was confirmed using spectral methods (FT-IR, 1H-NMR, 13C-NMR). The antibacterial activities of these compounds against Gram positive (Staphylococcus aureus ATCC 6583, Staphylococcus epidermidi...

Abdol Hajipour, Amin Zarei, Leila Khazdooz, Nafisehsadat Sheikhan

In the present of methylimidazolium hydrogen sulfate, the synthesis of arylidene heterobicyclic pyrimidinones is studied by condensation of aromatic aldehyde, cyclopentanone, and urea or thiourea. Using solvent-free conditions, non-toxic and inexpensive materials, simple and clean work-up, short reaction times and good yields of the products are the advantages of this method.

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