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Relevant bibliographies by topics / 3-d]pyrimidine-diones

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Academic literature on the topic '3-d]pyrimidine-diones'

Author: Grafiati

Published: 4 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "3-d]pyrimidine-diones"

1

Isakhanyan, A. U., N. Z. Hakobyan, Z. A. Hovasyan, et al. "Synthesis and effect of substituted pyrido[2,3-<i>d</i>]pyrimidine-2,4-diones on <i>In Vitro </i>tumor dna methylation." Журнал общей химии 93, no. 4 (2023): 525–30. http://dx.doi.org/10.31857/s0044460x23040042.

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Reaction of 3-diethylamino-1-aryl-, 3-diethylamino-1-aryl-2-phenyl(4-halophenyl)propane-1-ones hydrochlorides with 6-amino-1,3-dimethyluracil results in heterocyclization products, namely 1,3-dimethyl-7-aryl-5,6dihydro-1 H -pyrido[2,3- d ]pyrimidine-2,4-diones, 1,3-dimethyl-7-aryl-6-phenyl(4-halophenyl)-5,6-dihydro1 H -pyrido[2,3- d ]pyrimidine-2,4-diones and 1,3-dimethyl-7-aryl-6-phenyl-(4-halophenyl)-1 H -pyrido[2,3- d ] pyrimidine-2,4-diones. The effect of the synthesized compounds in vitro tumor DNA methylation was studied.

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2

Hamama, Wafaa S., Mohamed A. Ismail, Hana’a A. Al-Saman, and Hanafi H. Zoorob. "Convenient Selective Synthesis of Substituted Pyrido[2,3-d]pyrimidones and Annulated Derivatives." Zeitschrift für Naturforschung B 62, no. 1 (2007): 104–10. http://dx.doi.org/10.1515/znb-2007-0115.

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The reaction of 6-aminouracil (1) with the appropriate α,β -unsaturated ketones, gave the corresponding pyrido[2,3-d]pyrimidin-2,4-diones 3, 6, 8 and 10, respectively. Treatment of 1 with salicylaldehyde, 6-carboethoxy-3,5-diphenyl-2-cyclohexenone (13) or 2,6- bis(phenylmethylidene)cyclohexanone (15) afforded the corresponding pyrimido[4,5-d]quinoline- 2,4-diones 12, 14 and 16, respectively. Furthermore, a pyrido[2,3-d]pyrimidine incorporating 3,2’- bis(quinoline) derivative 18 was synthesized. Annulation of pyrido[2,3-d]pyrimidine with pyrazole or imidazole moieties was achieved via reaction

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3

Borrell, José I., Jordi Teixidó, Blanca Martínez-Teipel, et al. "An Unequivocal Synthesis of 4-Amino-1,5,6,8-tetrahydropyrido[2,3-d]pyrimidine-2,7-diones and 2-Amino-3,5,6,8-tetrahydropyrido[2,3-d]pyrimidine-4,7-diones." Collection of Czechoslovak Chemical Communications 61, no. 6 (1996): 901–9. http://dx.doi.org/10.1135/cccc19960901.

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An unequivocal set of procedures for the synthesis of 4-amino-1,5,6,8-tetrahydropyrido[2,3-d]pyrimidine-2,7-diones (7) and 2-amino-3,5,6,8-tetrahydropyrido[2,3-d]pyrimidine-4,7-diones (8), in a maximum of four steps from an α,β-unsaturated ester 1, is reported. Thus, the acid hydrolysis of the 2,4-diaminopyrido[2,3-d]pyrimidines 3 yields the 4-amino-2-oxopyrido[2,3-d]pyrimidines 7 while the cyclization of the Michael adducts 9 (formed by reaction of 1 and methyl cyanoacetate) with guanidine affords the corresponding 2-amino-4-oxopyrido[2,3-d]pyrimidines 8. Both isomers were also obtained by hy

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4

Daraie, Mansoureh, and Majid M. Heravi. "SMA/Py/ZnO as a new biocompatible polymer supported nanocatalyst for the synthesis of chromeno[2,3-d] pyrimidine-diones through a novel and efficient pathway." Canadian Journal of Chemistry 97, no. 11 (2019): 772–79. http://dx.doi.org/10.1139/cjc-2019-0127.

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An efficient and simple method for the synthesis of chromeno[2,3-d]pyrimidine-diones using SMA/Py/ZnO catalyst has been reported. Zinc oxide nanoparticles were coordinated on a modified poly(styrene-comaleic anhydride) (SMA) support to prevent agglomeration and reduction catalytic activity. The polymer support was easily prepared from the reaction of 3-aminopyridine with SMA. The catalyst was characterized by using various characterization techniques such as FTIR, 1H NMR, SEM, and EDX. The catalytic activity of SMA/Py/ZnO for the synthesis of chromeno[2,3-d]pyrimidine-diones through a multicom

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5

M, Heravi; Majid, and M. Daraie. "SMA/Py/ZnO as a new biocompatible polymer supported nanocatalyst for the synthesis of chromeno[2,3-d] pyrimidine-diones through a novel and efficient pathway." Canadian Journal of Chemistry 97, no. 11 (2019): 772–79. https://doi.org/10.1139/cjc-2019-0127.

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An efficient and simple method for the synthesis of chromeno[2,3-d]pyrimidine-diones using SMA/Py/ZnO catalyst has been reported. Zinc oxide nanoparticles were coordinated on a modified poly(styrene-comaleic anhydride) (SMA) support to prevent agglomeration and reduction catalytic activity. The polymer support was easily prepared from the reaction of 3-aminopyridine with SMA. The catalyst was characterized by using various characterization techniques such as FTIR,<sup>1</sup>H NMR, SEM, and EDX. The catalytic activity of SMA/Py/ZnO for the synthesis of chromeno[2,3-d]pyrimidine-diones through

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6

Tretyakov, N. A., M. V. Dmitriev, and A. N. Maslivets. "Synthesis of spiro(pyrrol-2,5'-pyrrolo[2,3-<i>d</i>]pyrimidine)2',4',5,6'-tetraones by the reaction of pyrrolo[2,1-<i>c</i>][1,4]oxazinetriones with 6-aminopyrimidine-2,4-diones." Журнал органической химии 59, no. 2 (2023): 180–86. http://dx.doi.org/10.31857/s0514749223020039.

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8-Aroyl-3,4-dihydro-1 H -pyrrolo[2,1- c ][1,4]oxazine-1,6,7-triones react with 6-aminopyrimidine-2,4(1 H ,3 H )diones to form 3-aroyl-4-hydroxy-1-(2-hydroxyalkyl)spiro(pyrrole-2,5'-pyrrolo[2,3- d ]pyrimidine)2',4',5,6'(1 H ,1' H ,3' H ,7' H )-tetraones, the structure of which was confirmed by X-ray diffraction analysis.

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7

Singh, Sonia, Mohammad H. Mosslemin, and Alireza Hassanabadi. "Synthesis of 5-Aryl-1,3-Dimethyl-7-Selenoxopyrimidino[4,5-d]Pyrimidine-2,4(1H,3H)-Dione." Journal of Chemical Research 42, no. 5 (2018): 264–66. http://dx.doi.org/10.3184/174751918x15265512038216.

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A one-pot method for the synthesis of six novel 5-aryl-1,3-dimethyl-7-selenoxopyrimidino[4,5- d]pyrimidine-2,4(1 H,3 H)-diones in excellent yields at room temperature has been achieved via reaction between potassium selenocyanate and an aroyl chloride followed by the addition of 6-amino- N,N′-dimethyluracil.

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8

Bogdanowicz-Szwed, Krystyna, та Aleksandra Pałasz. "Synthesis of 3,4-Dihydro-2H-pyrans by Hetero-Diels-Alder Reactions of Functionalized α,β-Unsaturated Carbonyl Compounds with Styrenes". Zeitschrift für Naturforschung B 56, № 4-5 (2001): 416–22. http://dx.doi.org/10.1515/znb-2001-4-515.

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Abstract Cycloadditions of 3-aryl-2-benzoyl-2-propenenitriles 1a,b to styrene (2a) and its methyl or methoxy-substituted derivatives 2b-d proceed regio- and diastereoselectively yielding cis and trans diastereoisomers of 2,4,6-triaryl-3,4-dihydro-2H-pyran-5-carbonitriles 3 and 4 in 59-72% yield. Cycloadducts cis-3 were the major products. Reaction of 5-(4-nitrobenzylidene)-1,3-dimethylbarbituric acid (5) with styrenes 2a-d afforded diastereoisomeric mixtures of 2H-pyrano[2,3-d]pyrimidine-2,4(3H)-diones cis-6 and trans-7 in 71 - 78% yield.

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9

Vlasov, Sergiy V., Hanna I. Severina, Oleksandr V. Borysov, et al. "Synthesis and Antimicrobial Evaluation of 2-(6-Imidazo[1,2-a]pyridin-2-yl-5-methyl-2,4-dioxo-3-phenyl-3,4-dihydrothieno[2,3-d]pyrimidin-1(2H)-yl)-N-arylacetamide Derivatives." Molbank 2022, no. 1 (2022): M1331. http://dx.doi.org/10.3390/m1331.

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6-Heteryl-5-methylthieno[2,3-d]pyrimidin-2,4(1H,3H)-diones are of great interest as the promising objects for the search of antibacterials. In this communication, we obtained 6-(imidazo[1,2-a]pyridin-2-yl)-5-methyl-3-phenylthieno[2,3-d]pyrimidine-2,4(1H,3H)-dione by interaction of 6-(bromoacetyl)-5-methyl-3-phenylthieno[2,3-d]pyrimidine-2,4(1H,3H)-dione with 2-aminopyridine. The obtained heterocyclic hybrid was further modified by alkylation with 2-chloroarylacetamides. Antimicrobial activity studies for the synthesized compounds using the agar well diffusion method revealed their moderate act

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10

Taghavi-Moghadam, Shahriyar, Rüdiger Stumpf, Helmut Fischer, and Wolfgang Pfleiderer. "Facile Synthesis of 6-Aryl-1,3-dimethyl-5H-pyrimido[4,5-b][1,4]diazepine-2,4(1H,3H)-diones." Collection of Czechoslovak Chemical Communications 64, no. 2 (1999): 313–20. http://dx.doi.org/10.1135/cccc19990313.

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A facile procedure for the preparation of 6-aryl-1,3-dimethyl-5H-pyrimido[4,5-b][1,4]diazepine2,4(1H,3H)-diones 8, 9 from 6-amino-5-arylideneamino-1,3-dimethyluracils 1, 2 and triethyl orthoacetate (3) in a two-step reaction via 6-aryl-8-ethoxy-6,7-dihydro-1,3-dimethyl-5H-pyrimido[4,5-b][1,4]diazepine-2,4(1H,3H)-diones 6, 7 is described. Condensation of 1 with diethoxymethyl acetate (10) resulted in the formation of (1,3-dimethyl-2,6-(1H,3H)-dioxopurin-7-yl)(phenyl)methyl acetate (11) and a small amount of 1,3-dimethyl-6-phenylpyrazino[2,3-d]pyrimidine-2,4(1H,3H)-dione (12). The structures of

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