Results 61 to 70 of about 227,778 (210)
As a part of ongoing studies in developing new anticancer agents, novel 1,2-dihydropyridine 4, thienopyridine 5, isoquinolines 6–20, acrylamide 21, thiazolidine 22, thiazoles 23–29 and thiophenes 33–35 bearing a biologically active quinoline nucleus were
Ghorab Mostafa M. +5 more
doaj +1 more source
2-Cyano-N-(thiazol-2-yl) acetamide (2a) and 2-cyano-N-(oxazol- 2-yl) acetamide (2b) were obtained via the reaction of ethyl cyanoacetate with either 2-aminothiazole (1a) or 2-aminooxazole (1b).
Albratty Mohammed +2 more
doaj +1 more source
Crystal Chemistry of Zinc Quinaldinate Complexes with Pyridine-Based Ligands
Substitution of methanol in [Zn(quin)2(CH3OH)2] (quin− denotes an anionic form of quinoline-2-carboxylic acid, also known as quinaldinic acid) with pyridine (Py) or its substituted derivatives, 3,5-lutidine (3,5-Lut), nicotinamide (Nia), 3 ...
Barbara Modec
doaj +1 more source
Pyridine-Based PCP-Ruthenium Complexes: Unusual Structures and Metal–Ligand Cooperation
Metal–ligand cooperation (MLC) by dearomatization/aromatization provides a unique way for bond activation, which has led to the discovery of various acceptorless dehydrogenative coupling reactions.
Shan Tang +17 more
core +1 more source
1-Allyl-2,3-cyclopentenopyridinium chloride
The title compound, C11H14N+·Cl−, was obtained by reaction of 2,3-cyclopentenopyridine and allyl chloride. A network of weak C—H...Cl hydrogen bonds is observed in the crystal structure.
Gabriel Partl +6 more
doaj +1 more source
Pyridine-Triggered Fluorescent Switching in Coordination-Induced Allosteric Crystal Transformation
Two zinc complexes with stimuli-responsive properties have been realized in [Zn(L)2] (1) and [Zn(L)2(py)]·py (2) (HL = N-(2-hydroxybenzylideneamino)-1,8-naphthalimide, py = pyridine). The crystal-to-crystal transformation between 1 and 2 is achieved by
Shufang Xue (1713094) +3 more
core +1 more source
Nickel-Mediated Dehydrogenative Aryl–Aryl Homocoupling of a Bulky Phosphino-Pyridine
Aryl–aryl bond formation through dehydrogenative coupling is an attractive transformation due to the atom and step economy of working with unfunctionalized C–H bonds. Pd catalysts are most common for this process, but Ni complexes have also been targeted
Kate A. Jesse (6871070) +2 more
core +1 more source
The Influence of Ratio Pyridine and Triethylamine Catalysts on Synthesis 2-Phenyl-Benzo [D][1, 3] Oxazine-4-On Derivatives [PDF]
The aim of this research was to compare the effect of pyridine and triethylamine catalyst ratios on the synthesis of 2-phenyl-benzo(d)[1,3] oxazine-4-one derivatives.
Galih Satrio Putra +5 more
core +2 more sources
In this work, four pyridine-based gemini and hetero-gemini gelator molecules have been designed which demonstrated aggregate-induced enhanced emission (AIEE) after gel formation in a DMSO/DMF:H2O mixture.
Sumita Roy (1549855) +3 more
core +1 more source
Pyridine-catalyzed atomic layer deposition (ALD) of SiO2 from hexachlorodisilane and water was studied by in situ analyses using Fourier-transform infrared spectrometry and a quartz crystal microbalance.
Hyeongjin Kim (14515275) +3 more
core +1 more source

