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Microbial Degradation of Pyridine and Pyridine Derivatives
2019Pyridine derivatives belong to an important class of aromatic compounds that occur largely as a result of human activities, although they are not necessarily xenobiotic compounds. Pyridines can also be derivatized to form a wide variety of xenobiotic compounds ranging from drugs to pesticides. Analogs to phenolic compounds, pyridines exhibit properties
Edward J. O'Loughlin +2 more
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ChemInform Abstract: Synthesis of Pluriaminated Pyridines.
ChemInform, 1998AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
A. DE MUNNO +4 more
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The FT-IR spectra of pyridine and pyridine-d5
Journal of Molecular Spectroscopy, 1984Abstract The high-resolution (0.06 cm−1) FT-IR spectra of pyridine and pyridine-d5 at various path lengths (up to 10 m) have been obtained. These spectra reveal many new features that were not observed before. For example, the observation of many difference bands allows accurate determination of vibrational term values of some inactive and/or weak ...
Steven D. Colson, Koon N. Wong
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SESQUITERPENE PYRIDINE ALKALOIDS
ChemInform, 2003AbstractFor Abstract see ChemInform Abstract in Full Text.
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Dipyrrylvinyl Pyridines as Trichuricides
Nature, 1964WHIPWORM infections in man and dog have been, until recent years, quite difficult to eradicate. During the past decade several compounds have been found to have activity against these worms. These compounds are ‘Phthalofyne’ orally1 or intravenously2, dithiazanine iodide3, stilbazium iodide4,5, and ‘Glycobiarsol’6.
R. B. Burrows, A. P. Phillips
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Chichibabin pyridine synthesis
2002Also known as the Chichibabin reaction. Condensation of aldehydes with ammonia to afford pyridines.
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The determination of the pyridine content of technical pyridine
The Analyst, 1946R. Pomfret, W. V. Stubbings, A. Hamer
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Nature, 1966
ALL the evidence at present available1 indicates that degradation of the pyridine nucleotides is the only biological source of nicotinamide, which can be formed by hydrolysis of the ribose–nicotinamide bond by enzymes of the NAD glycohydrolase (E.C. 3.2.2.5) class2.
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ALL the evidence at present available1 indicates that degradation of the pyridine nucleotides is the only biological source of nicotinamide, which can be formed by hydrolysis of the ribose–nicotinamide bond by enzymes of the NAD glycohydrolase (E.C. 3.2.2.5) class2.
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Reaction of Dichlorocarbene to Pyridines and Condensed Pyridines
HETEROCYCLES, 1980Yoshiki Hamada, Michiharu Suigura
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