Results 211 to 220 of about 7,405 (269)
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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.
Reidar Oftebro+3 more
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Metal-free radical C–H methylation of pyrimidinones and pyridinones with dicumyl peroxide
, 2017A new method for free radical methylation of pyrimidinones and pyridinones with dicumyl peroxide (DCP) under metal-free conditions is introduced. A 50 g-scale reaction could be performed safely at the desired concentration.
Pei-zhi Zhang+5 more
semanticscholar +1 more source
Synthesis, 2018
Mn(OAc)3-mediated alkoxycarbonylation of indoles, pyrimidinones, and pyridinones with alkyl carbazates is reported. The reactions proceed through a radical process to afford regioselectively 3-carboxylated indoles, 5-carboxylated pyrimidinones, and 3 ...
Cheng-Kun Li+6 more
semanticscholar +1 more source
Mn(OAc)3-mediated alkoxycarbonylation of indoles, pyrimidinones, and pyridinones with alkyl carbazates is reported. The reactions proceed through a radical process to afford regioselectively 3-carboxylated indoles, 5-carboxylated pyrimidinones, and 3 ...
Cheng-Kun Li+6 more
semanticscholar +1 more source
Regioselectivity in reactions of alkynylmetal complexes with pyrimidinones
Journal of Organometallic Chemistry, 1985Abstract Regioselectivity is observed in 1 1 -adduct formation between phenylethynyltriisopropoxytitanium and 2(1/ H )-pyrimidinones; the new carbon-carbon bond is formed at C(4). In contrast the 3,4- and 3,6-dihydro products are formed together from the corresponding magnesium and lithium reagents, but from the magnesium compound the major ...
Frode Rise, Kjell Undheim
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, 2017
A new series of azolopyrimidine derivatives incorporating pyrazole moiety were synthesized by reaction of 1-(pyrazol-3-yl)-2-propenone with a number of heterocyclic amines in the presence of a catalytic amount of acetic acid.
I. M. Abbas+3 more
semanticscholar +1 more source
A new series of azolopyrimidine derivatives incorporating pyrazole moiety were synthesized by reaction of 1-(pyrazol-3-yl)-2-propenone with a number of heterocyclic amines in the presence of a catalytic amount of acetic acid.
I. M. Abbas+3 more
semanticscholar +1 more source
ChemInform, 2012
AbstractThe efficient title reactions with anilines are achieved in pivalic acid as reaction medium.
Rhiannon Carter, Matthew L. Maddess
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AbstractThe efficient title reactions with anilines are achieved in pivalic acid as reaction medium.
Rhiannon Carter, Matthew L. Maddess
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(E)- and (Z)-Enamine Dewar Pyrimidinones [PDF]
The structures of (E)- and (Z)-methyl 1,6-dimethyl-5-oxo-2,6-diazabicyclo[2.2.0]hex-3-ylideneacetate, C 9 H 12 N 2 O 3 , have been established by X-ray diffraction analyses. The 2-azetidinone ring, azetidine ring and enamine moiety in both isomers are quite planar.
Y. Takahashi, S. i. Hirokami, H. Kakuda
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An efficient synthesis of thiazolo[3,2-a]pyrimidinones
Tetrahedron Letters, 2010AbstractThe short approach includes condensation of 2‐aminothiazoles with diesters (II) followed by cyclization in the presence of commercially available Eaton′s reagent.
Keith Jones, Nadia M. Ahmad
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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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Organic Letters, 2015
A divergent cascade annulation has been developed using readily available vinyl azides and carbazates with a wide range of substituents. Vinyl azides were successfully applied as bifunctional partners to prepare aza-pyrimidinones via 6-ring closure with ...
Jiaan Shao+6 more
semanticscholar +1 more source
A divergent cascade annulation has been developed using readily available vinyl azides and carbazates with a wide range of substituents. Vinyl azides were successfully applied as bifunctional partners to prepare aza-pyrimidinones via 6-ring closure with ...
Jiaan Shao+6 more
semanticscholar +1 more source