Results 211 to 220 of about 4,994 (242)
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ChemInform Abstract: Pyrimidinones. Part 1. 2‐Amino‐5‐halo‐6‐aryl‐4(3H)‐pyrimidinones.
Chemischer Informationsdienst, 1986AbstractDie aus dem Halbester (I) zugänglichem Pyrimidinone (V) besitzen Interferon‐induzierende und antivirale Wirkung.
H. I. SKULNICK +5 more
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Chemischer Informationsdienst, 1982
AbstractDie Photolyse der Pyrimidinone (I) in flüssigem Methylamin (II) führt zu den offenkettigen Produkten (III), die bei der Chromatographie an Aluminiumoxid zu den Pyrimidinonen (IV) cyclisieren.
Y. HIRAI +3 more
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AbstractDie Photolyse der Pyrimidinone (I) in flüssigem Methylamin (II) führt zu den offenkettigen Produkten (III), die bei der Chromatographie an Aluminiumoxid zu den Pyrimidinonen (IV) cyclisieren.
Y. HIRAI +3 more
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Pyrimidinone Antibiotics—Heterocyclic Analogues with Improved Antibacterial Spectrum.
ChemInform, 2003AbstractFor Abstract see ChemInform Abstract in Full Text.
Michael, Brands +5 more
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Antineoplastic properties of pyrimidinone interferon inducers
Advances in Enzyme Regulation, 1981Abstract The interferon inducing, antiviral and antitumor activities of a new series of pyrimidinone compounds are compared and summarized in this report. An interesting split in mechanism of action appeared to exist in these compounds. One group represented by ABPP were very potent interferon inducing agents and the antiviral and antitumor activity ...
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Conformation of 1,2,3,4-tetrahydro-2-pyrimidinones
Chemistry of Heterocyclic Compounds, 1981The conformation of a number of 1,2,3,4-tetrahydro-2-pyrimidinones with various substituents in the ring was established on the basis of the vicinal 3J34 constants found from the 1H NMR spectra of these compounds. It is shown that in solution rapid conformational transformations between the two possible “boat” conformations evidently occur.
�. �. Liepin'sh +2 more
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Pyrimidinones as reversible metaphase arresting agents
European Journal of Medicinal Chemistry, 1993Abstract 5-Halo- N (1)-substituted 2(1 H )-pyrimidinones have the ability to cause reversible arrest of mitosis during metaphase. Highly active compounds have a heteroatom ( O , S or N ) in the β-position of the N (1)-carbon chain which is further substituted by an aryl group. In vitro data have been provided.
T Benneche +3 more
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Phenylation of pyrimidinones using diphenyliodonium salts
Journal of the Chemical Society, Perkin Transactions 1, 1999Pyrimidinones 1 have been phenylated under basic conditions using diphenyliodonium salts, and the effect of substituents on the yield and regiochemistry has been studied.
Stig André Jacobsen +2 more
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Interferon Induction by 5-Halo-6-Phenyl Pyrimidinones
Journal of Interferon Research, 1980The interferon inducing characteristics of a new series of 6-phenyl pyrimidinol compounds are described and compared against a previously identified pyrimidine, 2-amino-5-bromo-6-methyl-4-pyrimidinol (ABMP). Interestingly, a split in ability to induce interferon but not in vivo antiviral activity was observed in the newest compounds. One representative
D A, Stringfellow +2 more
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4-Azido-2-pyrimidinone Nucleosides and Related Chemistry
The Journal of Organic Chemistry, 1997As a part of azide prodrug approach, we synthesized a 4-azido analog of ara-C (4) as a prodrug for ara-C. The compound 4 was obtained from 1-(beta-D-arabinofuranosyl)uracil (1) in three steps. At pH 7.0 and 11.0, a loss of UV absorption of the compound 4 was observed resulting from a transformation that was proved by identifying the transformed product
Lakshmi P., Kotra +7 more
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Syntheses of trifluoromethylated pyridinones and pyrimidinones
The Journal of Organic Chemistry, 1990Les syntheses s'effectuent via la reaction d'orthoformiates avec des enaminonitriles ou avec des ...
Len F. Lee, Y. Larry Sing
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