Log in

Relevant bibliographies by topics / Pyrimidinyl

Contents

Journal articles
Dissertations / Theses
Books
Book chapters
Conference papers
Reports

Academic literature on the topic 'Pyrimidinyl'

Author: Grafiati

Published: 4 June 2021

Last updated: 9 February 2022

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Pyrimidinyl.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "Pyrimidinyl"

1

Jiang, Duo Hua, and Gang Liu. "Synthesis and Properties Study of 1-(2,4-Dimethoxyl-5-Pyrimidinyl)-2-[2-Methyl-5-(3-Cyano)-3-Thienyl]Perfluorocyclopentene." Applied Mechanics and Materials 662 (October 2014): 91–94. http://dx.doi.org/10.4028/www.scientific.net/amm.662.91.

Full text

Abstract:

A novel photochromic diarylethene bearing a pyrimidine moiety, 1-(2,4-dimethoxyl-5-pyrimidinyl)-2-[2-methyl-5-(3-cyano)-3-thieny-l] perfluorocyclopentene has been synthesized. Its properties, including photochromic behavior and fluorescent properties, have been investigated. The compound exhibited remarkable photochromism, changing from colorless to blue after irradiation with UV light. The results indicated that the pyrimidine moiety played a very important role during the process of photoisomerization reactions.

APA, Harvard, Vancouver, ISO, and other styles

2

Kurth, Mark, Wonken Choung, Beth Lorsbach, Thomas Sparks, and James Ruiz. "4-(Isoxazol-3-yl)pyrimidines from Pyrimidinyl Nitrile Oxides." Synlett 2008, no. 19 (November 12, 2008): 3036–40. http://dx.doi.org/10.1055/s-0028-1087346.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

Hurst, DT, AD Stacey, M. Nethercleft, A. Rahim, and MR Harnden. "The Synthesis of Some Pyrimidinyl and Thiazolyl Ureas and Thioureas and Some Related Compounds." Australian Journal of Chemistry 41, no. 8 (1988): 1221. http://dx.doi.org/10.1071/ch9881221.

Full text

Abstract:

Some pyrimidin-2- and pyrimidin-4-amines were treated with isocyanates and isothiocyanates to give the corresponding disubstituted ureas or thioureas . A pyrimidin-2-amine is more reactive than a pyrimidin-4- amine in these reactions. 2-Aminothiazoles and thiazolinones also react to give the disubstituted ureas or thioureas . The use of ethoxycarbonyl or benzoyl isothiocyanate or isocyanate gives products which are readily hydrolysed to the pyrimidinyl or thiazolyureas or thioureas but with concomitant hydrolysis and decarboxylation of an ethoxycarbonyl substituent . The use of chlorosulfonyl or trimethylsilyl isocyanate gives the urea derivative without isolation of the intermediate disubstituted urea. Some related compounds were also synthesized.

APA, Harvard, Vancouver, ISO, and other styles

4

Sharma, Vijay Kumar, Anup Barde, and Sunita Rattan. "Design, Synthesis and Characterization of Pyrimidine based Thiazolidinedione Derivatives." Asian Journal of Chemistry 32, no. 5 (2020): 1101–8. http://dx.doi.org/10.14233/ajchem.2020.22565.

Full text

Abstract:

Novel thiazolidine-2,4-dione (TZD) based pyrimidine derivatives have been synthesized by Knoevenagel condensation reaction between thiazolidine-2,4-dione and amino pyrimidinyl aliphatic aldehydes followed by heterogeneous metal reduction. Synthetic strategy involved nucleophillic substitution of hydroxyl protected six membered aliphatic chain on 4,6-dichloropyrimidine followed by Suzuki coupling. This approach is regioselective, efficient and versatile for synthesis of such analogs

APA, Harvard, Vancouver, ISO, and other styles

5

Liu, Jing Jing, Hong Jing Jia, and Shou Zhi Pu. "Synthesis and Properties Study of 1-(2,4-dimethoxyl-5-pyrimidinyl)-2-[2-methyl-5-(9-phenanthrene)-3-thienyl] perfluorocyclopentene." Advanced Materials Research 1003 (July 2014): 31–34. http://dx.doi.org/10.4028/www.scientific.net/amr.1003.31.

Full text

Abstract:

A novel photochromic diarylethene bearing a pyrimidine moiety, 1-(2,4-dimethoxyl-5-pyrimidinyl)-2-[2-methyl-5-(9-phenanthrene)-3-thienyl] perfluorocyclopentene has been synthesized. Its properties, including photochromic behavior and fluorescent properties, have been investigated. The compound exhibited remarkable photochromism, changing from colorless to red after irradiation with UV light in solution. The fluorescence had a remarkable initial increase with subsequent dramatic decrease with increasing concentration. The results indicated that the pyrimidine moiety played a very important role during the process of photoisomerization reactions.

APA, Harvard, Vancouver, ISO, and other styles

6

Liu, Jing Jing, Hong Jing Jia, and Shou Zhi Pu. "Synthesis and Properties Study of 1-(2,4-dimethoxyl-5-pyrimidinyl)-2-[2-methyl-5-(4-n-pentylbenzene)-3-thienyl] Perfluorocyclopentene." Advanced Materials Research 952 (May 2014): 75–78. http://dx.doi.org/10.4028/www.scientific.net/amr.952.75.

Full text

Abstract:

A novel photochromic diarylethene based on a six-membered pyrimidine moiety 1-(2,4-dimethoxyl-5-pyrimidinyl)-2-[2-methyl-5-(4-n-pentylbenzene)-3-thienyl] perfluorocyclopent-ene has been synthesized. Its properties, including photochromic behavior and fluorescent properties, have been investigated. The compounds exhibited remarkable photochromism, changing from colorless to red after irradiation with UV light both in solution and in PMMA film. The fluorescence had a remarkable initial increase with subsequent dramatic decrease with increasing concentration. The results indicated that the pyrimidine moiety played a very important role during the process of photoisomerization reactions.

APA, Harvard, Vancouver, ISO, and other styles

7

Brough, Peter, Jacques Pécaut, André Rassat, and Paul Rey. "Pyrimidinyl Nitronyl Nitroxides." Chemistry - A European Journal 12, no. 19 (June 23, 2006): 5134–41. http://dx.doi.org/10.1002/chem.200600061.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

Wang, Hsiao-Fen, Kuang-Hway Yih, and Gene-Hsiang Lee. "Syntheses, Reactivities, Characterization, and Crystal Structures of Dipalladium Complexes Containing the 1,3-pyrimidinyl Ligand: Structures of [Pd(PPh3)(Br)]2(μ,η2-C4H3N2)2, [Pd(Br)]2(μ,η2-Hdppa)2, and [{Pd(PPh3)(CH3CN)}2(μ,η2-C4H3N2)2][BF4]2." Molecules 25, no. 9 (April 27, 2020): 2035. http://dx.doi.org/10.3390/molecules25092035.

Full text

Abstract:

In a refluxing chloroform solution, the η1-pyrimidinyl {pyrimidinyl = C4H3N2} palladium complex [Pd(PPh3)2(η1-C4H3N2)(Br)], 1 exhibited intermolecular displacement of two triphenylphosphine ligands to form the doubly bridged η2-pyrimidinyl Dipalladium complex [Pd(PPh3)(Br)]2(μ,η2-C4H3N2)2, 3. The treatment of 1 with Hdppa {Hdppa = N,N-bisdiphenyl phosphinoamine} in refluxing dichloromethane yielded the doubly bridged Hdppa dipalladium complex [Pd(Br)]2(μ,η2-Hdppa)2, 4. Complex 1 reacted with the bidentate ligand, NH4S2CNC4H8 and, NaS2COEt, and the tridentate ligand, KTp {Tp = tris(pyrazoyl-1-yl)borate}, to form the η2-dithio η1-pyrimidinyl complex [Pd(PPh3)(η1-C4H3N2)(η2-SS)], (5: SS = S2CNC4H8; 6: SS = S2COEt) and η2-Tp η1-pyrimidinyl complex [Pd(PPh3)(η1-C4H3N2)(η2-Tp)], 7, respectively. Treatment of 1 with AgBF4 in acetonitrile at room temperature resulted in the formation of the doubly bridged η2-pyrimidinyl dipalladium complex [{Pd(PPh3)(CH3CN)}2(μ,η2-C4H3N2)2][BF4]2, 8. All of the complexes were identified using spectroscopic methods, and complexes 3, 4, and 8 were determined using single-crystal X-ray diffraction analyses.

APA, Harvard, Vancouver, ISO, and other styles

9

Voigt, Harry, Dietrich Heydenhauß, Frank Hofmann, and Günter Jaenecke. "Gemischte Pyrimidinyl-azolyl-thioäther." Zeitschrift für Chemie 14, no. 12 (September 1, 2010): 472. http://dx.doi.org/10.1002/zfch.19740141208.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

Smicius, Romualdas, Virginija Jakubkiene, Milda M. Burbuliene, Aiste Mikalainyte, and Povilas Vainilavicius. "Synthesis of 1-(6-Methyl-2,4-Dioxo-1,2,3,4-Tetrahydro-3-Pyrimidinyl)Acetyl-4-Alkyl(Aryl)Thiosemicarbazides and their Heterocyclisation to 1,2,4-Triazoles and 1,3,4-Thiadiazoles." Journal of Chemical Research 2002, no. 4 (April 2002): 170–72. http://dx.doi.org/10.3184/030823402103171555.

Full text

Abstract:

5-(6-Methyl-2,4-dioxo-1,2,3,4-tetrahydro-3-pyrimidinyl)methyl-1,3,4-oxadiazole-2-thione reacts with amines to give 1-(6-methyl-2,4-dioxo-1,2,3,4-tetrahydro-3-pyrimidinyl)acetyl-4-alkyl(aryl)thiosemicarbazides, which on treatment with base or acid undergo cyclisation to 4-alkyl-1,2,4-triazole-2-thiones or 4-amino-1,3,4-thiadiazoles, respectively.

APA, Harvard, Vancouver, ISO, and other styles

More sources

Dissertations / Theses on the topic "Pyrimidinyl"

1

Bouillon, Alexandre. "Les acides et esters halogenopyridinyl et pyrimidinyl boroniques : synthèse et étude physicochimique." Caen, 2003. http://www.theses.fr/2003CAEN4064.

Full text

APA, Harvard, Vancouver, ISO, and other styles

2

Spencer, Keith. "Parallel synthesis of C-nucleosides." Thesis, University of Oxford, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.325958.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

Xu, Kuiying. "Pyrrolo[2,3-d]pyrimidine, Pyrazolo[3,4-d]pyrimidine and Triazolo[4,5-d]pyrimidine nucleosides and oligonucleotides: Synthesis, physical properties and base-pairing = Pyrrolo[2,3-d]pyrimidin, Pyrazolo[3,4-d]pyrimidin und Triazolo[4,5-d]pyrimidin nucleoside und oligonucleotide: Synthese, physikalische Eigenschaften und Basenpaarung /." Osnabrück, 2008. http://opac.nebis.ch/cgi-bin/showAbstract.pl?sys=000254557.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

Ibrahim, Mohamed M. "Pyrimidine Metabolism in Rhizobium: Physiological Aspects of Pyrimidine Salvage." Thesis, University of North Texas, 1989. https://digital.library.unt.edu/ark:/67531/metadc330907/.

Full text

Abstract:

The objective of this research was to study the pyrimidine salvage pathways of Rhizobium. Three approaches were used to define the pyrimidine salvage pathways operative in two species of Rhizobium, R. meliloti and R. leguminosarum . The first approach was to ascertain the pyrimidine bases and nucleosides that could satisfy the pyrimidine requirement of pyrimidine auxotrophs. Uracil, cytosine, uridine or cytidine all satisfied the absolute pyrimidine requirement. The second approach was to select for mutants resistant to 5-fluoropyrimidine analogues which block known steps in the interconversion of the pyrimidine bases and nucleosides. Mutants resistant to 5-fluorouracil lacked the enzyme uracil phosphoribosyltransferase (upp ) and could no longer use uracil to satisfy their pyrimidine requirement. Mutants resistant to 5-fluorocytosine, while remaining sensitive to 5- fluorouracil, lacked cytosine deaminase (cod) and thus could no longer use cytosine to satisfy their pyrimidine auxotrophy. The third approach used a reversed phase HPLC column to identify the products that accumulated when cytidine, uridine or cytosine was incubated with cell extracts of wild type and analogue resistant mutants of Rhizobium. When cytidine was incubated with cell extracts of Rhizobium wild type, uridine, uracil and cytosine were produced. This Indicated that Rhizobium had an active cytidine deaminase (cdd) and either uridine phosphorylase or uridine hydrolase. By dialyzing the extract and reincubating it with cytidine, uridine and uracil still appeared. This proved that it was a hydrolase ( nuh ) rather than a phosphorylase that degraded the nucleoside. Thus, Rhizobium was found to contain an active cytidine deaminase and cytosine deaminase with no uridine phosphorylase present. The nucleoside hydrolase was active with cytidine, uridine and to a far lesser extent with purines, adenosine and inosine. When high concentrations of cytidine were added to mutants devoid of hydrolase, cytosine was produced from cytidine - 5-monophosphate by the sequential action of uridine ( cytidine ) kinase and nucleoside monophosphate glycosylase. Both ft meliloti and ft leguminosarum had identical salvage pathways.

APA, Harvard, Vancouver, ISO, and other styles

5

Beck, Debrah A. (Debrah Ann). "Pyrimidine Salvage Enzymes in Microorganisms: Labyrinths of Enzymatic Diversity." Thesis, University of North Texas, 1995. https://digital.library.unt.edu/ark:/67531/metadc278204/.

Full text

Abstract:

Pyrimidine salvage pathways are essential to all cells. They provide a balance of RNA synthesis with the biosynthetic pathway in pyrimidine prototrophs and supply all the pyrimidine requirements in auxotrophs. While the pyrimidine biosynthetic pathway is found in almost all organisms and is nearly identical throughout nature, the salvage pathway often differs from species to species, with aspects of salvage seen in every organism. Thus significant taxonomic value may be ascribed to the salvage pathway. The pyrimidine salvage pathways were studied in 55 microorganisms. Nine different salvage motifs, grouped I-IX, were identified in this study based on the presence of different combinations of the following enzymes: cytidine deaminase (Cdd), cytosine deaminase (Cod), uridine phosphorylase (Udp), uracil phosphoribosyltransferase (Upp), uridine hydrolase (Udh), nucleoside hydrolase (Nuh), uridine/cytidine kinase (Udk), 5'-nucleotidase and CMP kinase (Cmk).

APA, Harvard, Vancouver, ISO, and other styles

6

Roush, Wendy A. "Pyrimidine Genes in Pseudomonas Species." Thesis, University of North Texas, 2003. https://digital.library.unt.edu/ark:/67531/metadc4395/.

Full text

Abstract:

This thesis is a comparative study of gene arrangements in Pseudomonas species, and is organized into three major sections. The first section compares gene arrangements for different pathways in Pseudomonas aeruginosa PAO1 to determine if the gene arrangements are similar to previous studies. It also serves as a reference for pyrimidine gene arrangements in P. aeruginosa. The second part compares the physical, and genetic maps of P. aeruginosa PAO1 with the genome sequence. The final section compares pyrimidine gene arrangements in three species of Pseudomonas. Pyrimidine biosynthesis and salvage genes will be aligned for P. aeruginosa PAO1, P. putida KT2440, and P. syringae DC3000. The whole study will gives insight into gene patterns in Pseudomonas, with a focus on pyrimidine genes.

APA, Harvard, Vancouver, ISO, and other styles

7

Hughes, Lee E. (Lee Everette). "Pyrimidine Metabolism in Streptomyces griseus." Thesis, University of North Texas, 1994. https://digital.library.unt.edu/ark:/67531/metadc278710/.

Full text

Abstract:

Salvage of pyrimidine nucleosides and bases by S. griseus and the regulation of aspartate transcarbamoylase (ATCase) were studied. The velocity-substrate curve for S. griseus ATCase was hyperbolic for both aspartate and carbamoylphosphate. The enzyme activity was diminished in the presence of ATP, CTP, or UTP. The synthesis of ATCase was repressed in cells grown in the presence of exogenous uracil. The specific activity of cells grown with uracil was 43 percent of that for cells grown in minimal medium only. Maximal ATCase and dihydroorotase activities were found in the same column fraction after size-exclusion chromatography, suggesting that both activities could reside in the same polypeptide. The pyrimidine salvage enzymes cytosine deaminase and uridine phosphorylase were identified in S. griseus using HPLC reversed-phase chromatography.

APA, Harvard, Vancouver, ISO, and other styles

8

Asfour, Hani. "Regulation of pyrimidine biosynthesis and virulence factor production in wild type, Pyr- and Crc- mutants in Pseudomonas aeruginosa." Thesis, University of North Texas, 2006. https://digital.library.unt.edu/ark:/67531/metadc5297/.

Full text

Abstract:

Previous research in our laboratory established that pyrB, pyrC or pyrD knock-out mutants in Pseudomonas aeruginosa required pyrimidines for growth. Each mutant was also discovered to be defective in the production of virulence factors. Moreover, the addition of exogenous uracil did not restore the mutant to wild type virulence levels. In an earlier study using non-pathogenic P. putida, mutants blocked in one of the first three enzymes of the pyrimidine pathway produced no pyoverdine pigment while mutants blocked in the fourth, fifth or sixth steps produced copious quantities of pigment, just like wild type P. putida. The present study explored the correlation between pyrimidine auxotrophy and pigment production in P. aeruginosa. Since the pigment pyoverdine is a siderophore it may also be considered a virulence factor. Other virulence factors tested included casein protease, elastase, hemolysin, swimming, swarming and twitching motilities, and iron binding capacity. In all cases, these virulence factors were significantly decreased in the pyrB, pyrC or pyrD mutants and even in the presence of uracil did not attain wild type levels. In order to complete this comprehensive study, pyrimidine mutants blocked in the fifth (pyrE) and sixth (pyrF) steps of the biosynthetic pathway were examined in P. aeruginosa. A third mutant, crc, was also studied because of its location within 80 base pairs of the pyrE gene on the P. aeruginosa chromosome and because of its importance for carbon source utilization. Production of the virulence factors listed above showed a significant decrease in the three mutant strains used in this study when compared with the wild type. This finding may be exploited for novel chemotherapy strategies for ameliorating P. aeruginosa infections in cystic fibrosis patients.

APA, Harvard, Vancouver, ISO, and other styles

9

Hughes, Lee E. (Lee Everette). "Pyrimidine Biosynthesis in the Genus Streptomyces : Characterization of Aspartate Transcarbamoylase and Its Interaction with Other Pyrimidine Enzymes." Thesis, University of North Texas, 1998. https://digital.library.unt.edu/ark:/67531/metadc278797/.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

Patel, Monal V. "The regulatory roles of PyrR and Crc in pyrimidine metabolism in Pseudomonas aeruginosa." Thesis, University of North Texas, 2001. https://digital.library.unt.edu/ark:/67531/metadc2875/.

Full text

Abstract:

The regulatory gene for pyrimidine biosynthesis has been identified and designated pyrR. The pyrR gene product was purified to homogeneity and found to have a monomeric molecular mass of 19 kDa. The pyrR gene is located directly upstream of the pyrBC' genes in the pyrRBC' operon. Insertional mutagenesis of pyrR led to a 50- 70% decrease in the expression of pyrBC', pyrD, pyrE and pyrF while pyrC was unchanged. This suggests that PyrR is a positive activator. The upstream regions of the pyrD, pyrE and pyrF genes contain a common conserved 9 bp sequence to which the purified PyrR protein is proposed to bind. This consensus sequence is absent in pyrC but is present, as an imperfect inverted repeat separated by 11 bp, within the promoter region of pyrR. Gel retardation assays using upstream DNA fragments proved PyrR binds to the DNA of pyrD, pyrE, pyrF as well as pyrR. This suggests that expression of pyrR is autoregulated; moreover, a stable stem-loop structure was determined in the pyrR promoter region such that the SD sequence and the translation start codon for pyrR is sequestered. β-galactosidase activity from transcriptional pyrR::lacZ fusion assays, showed a two-fold in increase when expressed in a pyrR- strain compared to the isogenic pyrR+ strain. Thus, pyrR is negatively regulated while the other pyr genes (except pyrC) are positively activated by PyrR. That no regulation was seen for pyrC is in keeping with the recent discovery of a second functional pyrC that is not regulated in P. aeruginosa. Gel filtration chromatography shows the PyrR protein exists in a dynamic equilibrium, and it is proposed that PyrR functions as a monomer in activating pyrD, pyrE and pyrF and as a dimeric repressor for pyrR by binding to the inverted repeat. A related study discovered that the catabolite repression control (Crc) protein was indirectly involved in pyr gene regulation, and shown to negatively regulate expression of PyrR at the posttranscriptional level.

APA, Harvard, Vancouver, ISO, and other styles

More sources

Books on the topic "Pyrimidinyl"

1

Brown, D. J. Pyrimidines. New York: Wiley, 1993.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

2

International Symposium on Human Purine and Pyrimidine Metabolism (6th 1988 Hakone-machi, Japan). Purine and pyrimidine metabolism in man VI. New York: Plenum Press, 1989.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

3

The pyrimidines. New York: Wiley, 1994.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

4

1926-, Nyhan William L., Thompson L. F. 1947-, Watts R. W. E, and Seegmiller J. E, eds. Purine and pyrimidine metabolism in man V. New York: Plenum Press, 1986.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

5

Delia, Thomas J. Miscellaneous fused pyrimidines. New York: Wiley, 1992.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

6

Griffin, Roger John. Novel biological roles for pyrimidines. Birmingham: Aston University. Department of Pharmaceutical Sciences, 1986.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

7

Pharmacology of purine and pyrimidine receptors. San Diego, CA: Elsevier, 2011.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

8

Pfleiderer, Mathias. Synthese und Eigenschaften 6-substituierter Pyrido[2,3-d]pyrimidine. Konstanz: Hartung-Gorre, 1986.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

9

Scott, Andrew William. Preparation of fluorinated pyrrolo[2,3-d]pyrimidine. Birmingham: University of Birmingham, 1995.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

10

International Symposium on Purine and Pyrimidine Metabolism in Man (7th 1991 Bournemouth, England). Purine and pyrimidine metabolism in man VII. New York: Plenum Press, 1991.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

More sources

Book chapters on the topic "Pyrimidinyl"

1

Ann Hanagan, Mary, and Atul Puri. "Pyrimidinyl and Triazinylsulfonylurea Herbicides." In Bioactive Heterocyclic Compound Classes, 39–50. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527664412.ch3.

Full text

APA, Harvard, Vancouver, ISO, and other styles

2

Johnson, Peter L., Ronald E. Hackler, Joel J. Sheets, Tom Worden, and James Gifford. "Synthesis and Insecticidal Activity ofN-(4-Pyridinyl and Pyrimidinyl)phenylacetamides." In ACS Symposium Series, 136–46. Washington, DC: American Chemical Society, 1998. http://dx.doi.org/10.1021/bk-1998-0686.ch014.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

MacCoss, M., and M. J. Robins. "Anticancer pyrimidines, pyrimidine nucleosides and prodrugs." In The Chemistry of Antitumour Agents, 261–98. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0397-5_9.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

Pardasani, R. T., and P. Pardasani. "Magnetic properties of 1, 3-pyrimidinyl(2, 4, 6-pyrimidinetrione) chelate of copper(II)." In Magnetic Properties of Paramagnetic Compounds, 542–43. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49202-4_259.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

Winkelmann, Jochen. "Diffusion coefficient of 4-amino-N-2-pyrimidinyl-benzenesulfonamide into water, tris(hydroxymethyl)-aminomethane and hydrogen chloride solution." In Diffusion in Gases, Liquids and Electrolytes, 1502. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_1272.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

Dudaş, Nicoleta A., and Mihai V. Putz. "Pyrimidines." In New Frontiers in Nanochemistry, 445–70. Includes bibliographical references and indexes. | Contents: Volume 1. Structural nanochemistry – Volume 2. Topological nanochemistry – Volume 3. Sustainable nanochemistry.: Apple Academic Press, 2020. http://dx.doi.org/10.1201/9780429022937-41.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Mehlhorn, Heinz. "Pyrimidines." In Encyclopedia of Parasitology, 2297–98. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-43978-4_2622.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

Brown, E. G. "Pyrimidines." In Ring Nitrogen and Key Biomolecules, 88–127. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-4906-8_5.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

Mehlhorn, Heinz. "Pyrimidines." In Encyclopedia of Parasitology, 1–2. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-27769-6_2622-2.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

Li, Jie Jack, and Minmin Yang. "Pyrimidines." In Drug Discovery with Privileged Building Blocks, 209–18. Boca Raton: CRC Press, 2021. http://dx.doi.org/10.1201/9781003190806-24.

Full text

APA, Harvard, Vancouver, ISO, and other styles

Conference papers on the topic "Pyrimidinyl"

1

Liu, J. J., H. L. Liu, and S. Z. Pu. "Synthesis and Properties Study of 1-(2,4-dimethoxyl-5-pyrimidinyl)-2-[2-methyl-5-(3-methyl)-phenyl-3-thienyl] Perfluorocyclopentene." In International Conference on Materials Chemistry and Environmental Protection 2015. Paris, France: Atlantis Press, 2016. http://dx.doi.org/10.2991/meep-15.2016.21.

Full text

APA, Harvard, Vancouver, ISO, and other styles

2

Gharib, Ali, Mina Roshani, and Manouchehr Jahangir. "Efficient Catalytic Synthesis of Pyrazolo[3,4-d]pyrimidine, Pyrazolo[4,3- e][1,2,4]triazolo[1,5-c]pyrimidine, Pyrazolo[4,3-e][1,2,4]triazolo[1,5- c]pyrimidine, Pyrazolo[3,4-d]pyrimidin-4-one derivatives using Heterogeneous Preyssler Heteropolyacid, H₁₄[NaP₅W₃₀O₁₁0]/SiO₂." In The 13th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2009. http://dx.doi.org/10.3390/ecsoc-13-00169.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

Slivka, Mar V., M. M. Fizer, D. Zh Bereksazi, R. T. Mariychuk, A. O. Kryvoviaz, V. G. Lendel, N. P. Khripak, G. M. Koval, and Mikh V. Slivka. "Preparation of Bioactive Fused Pyrimidines via Environmental Technologies." In 2019 International Council on Technologies of Environmental Protection (ICTEP). IEEE, 2019. http://dx.doi.org/10.1109/ictep48662.2019.8968984.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

Hou, Minmei, Louxin Zhang, and Robert S. Harris. "Alignment seeding strategies using contiguous pyrimidine purine matches." In the ACM Conference. New York, New York, USA: ACM Press, 2012. http://dx.doi.org/10.1145/2382936.2382985.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

Kelly, John, and Nathan Hammer. "SPECTROSCOPIC AND COMPUTATIONAL CHARACTERIZATION OF HYDRATED PYRIMIDINE ANIONS." In 69th International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2014. http://dx.doi.org/10.15278/isms.2014.fb12.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

Šimák, Ondřej, Petr Pachl, Tomáš Jandušík, Jiří Brynda, Miloš Buděšínský, and Ivan Rosenberg. "Bi-substrate inhibitors of human pyrimidine 5’-nucleotidases." In XVIth Symposium on Chemistry of Nucleic Acid Components. Prague: Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2014. http://dx.doi.org/10.1135/css201414381.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Sivapriya, S., S. Priyanka, D. Sivakumar, M. Gopalakrishnan, M. Seenivasan, and H. Manikandan. "Experimental and optimized studies of some pyrimidine derivatives." In INTERNATIONAL CONFERENCE ON RECENT TRENDS IN APPLIED MATHEMATICAL SCIENCES (ICRTAMS-2020). AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0063017.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

Shutalev, Anatoly, and Anastasia Fesenko. "A Novel Ring Expansion of Pyrimidines to 1,2,4-Triazepines." In The 20th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-a018.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

Mukhin, E., V. Fedotov, E. Ulomsky, and V. Rusinov. "NON-NATURAL NUCLEOSIDES BASED ON AZOLO[1,5-A]PYRIMIDINES." In Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m771.aks-2019/279-280.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

Koos, M., B. Steiner, and J. Gajdos. "Synthesis of Some Sulfur Bridged Pyrimidines, Pyrazoles and Imidazoles." In The 1st International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 1997. http://dx.doi.org/10.3390/ecsoc-1-02002.

Full text

APA, Harvard, Vancouver, ISO, and other styles

Reports on the topic "Pyrimidinyl"

1

Kiessling, L. L., and P. B. Dervan. Analysis of Nearest Neighbor Interactions in the Pyrimidine Triple Helix Motif by Affinity Cleaving. Fort Belvoir, VA: Defense Technical Information Center, June 1991. http://dx.doi.org/10.21236/ada237527.

Full text

APA, Harvard, Vancouver, ISO, and other styles

2

Amy, Penny. Enzyme reactions using ureidosuccinate as a substrate during pyrimidine biosynthesis and degradation in Cl. oroticum. Portland State University Library, January 2000. http://dx.doi.org/10.15760/etd.2151.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

Cao, Deliang, and Giuseppe Pizzorno. P53 Regulation of Uridine Phosphorylase Activity Pyrimidine Salvage Pathway and Their Effects on Breast Cancer Therapy. Fort Belvoir, VA: Defense Technical Information Center, July 2001. http://dx.doi.org/10.21236/ada395919.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

Cao, Deliang, and Giuseppe Pizzorno. P53 Regulation of Uridine Phosphorylase Activity, Pyrimidine Salvage Pathway and Their Effects on Breast Cancer Therapy. Fort Belvoir, VA: Defense Technical Information Center, July 2003. http://dx.doi.org/10.21236/ada418743.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

Griffin, L. C., L. L. Kiessling, and P. B. Dervan. Recognition of All Four Base Pairs of Duplex DNA by Triple Helix Formation. Design of Pyrimidine Specific Bases. Fort Belvoir, VA: Defense Technical Information Center, June 1991. http://dx.doi.org/10.21236/ada237360.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

Wallace, Susan S. Structure/Function Analysis of DNA-glycosylases That Repair Oxidized Purines and Pyrimidines and the Influence of Surrounding DNA Sequence on Their Interactions. Office of Scientific and Technical Information (OSTI), August 2005. http://dx.doi.org/10.2172/900301.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Manson, J. L., D. M. Jasen, John Singleton, and P. A. Goddard. Pulsed-field magnetization of frustrated S = 1/2 Cu(pyrimidine)_1.5(H₂O)(BF₄)₂. Office of Scientific and Technical Information (OSTI), February 2017. http://dx.doi.org/10.2172/1343723.

Full text

APA, Harvard, Vancouver, ISO, and other styles

We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!