Results 11 to 20 of about 24,216 (244)

ON PYRIDINE HEMOCHROMOGEN [PDF]

open access: yesJournal of General Physiology, 1929
1. Cyanide hemochromogen probably contains one cyanide group per heme group. 2. The equilibrium between pyridine hemochromogen and its components, pyridine and reduced heme, is complicated to an unknown extent by the precipitation of reduced heme and the aggregation of pyridine hemochromogen. 3.
A E, Mirsky, M L, Anson
openaire   +2 more sources

From Pyridine to (−)‐Agelastatin A

open access: yesAdvanced Synthesis & Catalysis, 2023
Abstract(−)‐Agelastatin A was synthetized employing a flow photorearrangement of a pyridinium salt, constructing in one step the cyclopentene core possessing the desired functionalities and relative configurations. A flow enzymatic kinetic resolution of the resulting bicyclic vinyl aziridine delivered the enantiopure precursor to the natural product ...
Vale, João R.   +5 more
openaire   +4 more sources

Metastable Transitions in Pyridine and Pyridine Derivatives [PDF]

open access: yesZeitschrift für Naturforschung A, 1981
The kinetic energy released in metastable transitions in pyridine, 2, 3, 4 acetylpyridine and 2, 3, 4 aminopyridine differs for the different isomers. This indicates that the dissociation path-way of these compounds depends on the position of the nitrogen atom in the isomer.
Th. M. El-Sherbini   +2 more
openaire   +1 more source

Pyridine [PDF]

open access: yesThe American Journal of the Medical Sciences, 1894
n ...
openaire   +2 more sources

An Efficient Synthesis of Novel Pyrazole-Based Heterocycles as Potential Antitumor Agents

open access: yesApplied Sciences, 2017
A new series of pyrazolylpyridines was prepared by reaction of ethyl-3-acetyl-1,5-diphenyl-1H-pyrazole-4-carboxylate with the appropriate aldehyde, malononitrile, or ethyl acetoacetate and an excess of ammonium acetate under reflux in acetic acid ...
Magda A. Abdallah   +5 more
doaj   +1 more source

Synthesis, Molecular Docking Study, and Cytotoxicity Evaluation of Some Novel 1,3,4-Thiadiazole as Well as 1,3-Thiazole Derivatives Bearing a Pyridine Moiety

open access: yesMolecules, 2022
Pyridine, 1,3,4-thiadiazole, and 1,3-thiazole derivatives have various biological activities, such as antimicrobial, analgesic, anticonvulsant, and antitubercular, as well as other anticipated biological properties, including anticancer activity.
Amr S. Abouzied   +7 more
doaj   +1 more source

Bohlmann-Rahtz Cyclodehydration of Aminodienones to Pyridines Using N-Iodosuccinimide

open access: yesMolecules, 2010
Cyclodehydration of Bohlmann-Rahtz aminodienone intermediates using N-iodosuccinimide as a Lewis acid proceeds at low temperature under very mild conditions to give the corresponding 2,3,6-trisubstituted pyridines in high yield and with total ...
Mark C. Bagley, Christian Glover
doaj   +1 more source

Electron-Deficient Acetylenes as Three-Modal Adjuvants in SNH Reaction of Pyridinoids with Phosphorus Nucleophiles

open access: yesMolecules, 2021
Publications covering a new easy metal-free functionalization of pyridinoids (pyridines, quinolines, isoquinolines, acridine) under the action of the system of electron-deficient acetylenes (acetylenecarboxylic acid esters, acylacetylenes)/P-nucleophiles
Boris A. Trofimov   +2 more
doaj   +1 more source

Discovering the stacking landscape of a pyridine-pyridine system [PDF]

open access: yesJournal of Molecular Modeling, 2017
Extremely extensive calculations of potential energy surfaces for the parallel-displaced configuration of pyridine dimer systems have been carried out using a dispersion-corrected density functional. Instead of focusing on stationary geometries these calculations provide much deeper insight into the "landscape" of the interaction energies of the ...
openaire   +2 more sources

Pyridine-Based Heterocycles. Synthesis of New Pyrido [4',3':4,5]thieno[2,3-d]pyrimidines and Related Heterocycles

open access: yesMolecules, 2010
The synthesis of the title compounds was achieved using ethyl 2-amino-6-methyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxylate (1) as starting material.
Hussein El-Kashef   +4 more
doaj   +1 more source

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