Relevant bibliographies by topics / Pyrimidine synthesis

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Pyrimidine synthesis'

Author: Grafiati
Published: 4 June 2021
Last updated: 26 July 2025

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 'Pyrimidine synthesis.'

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 "Pyrimidine synthesis"

1

Verma, Vishal, Chandra Prakash Joshi, Alka Agarwal, Sakshi Soni, and Udichi Kataria. "A Review on Pharmacological Aspects of Pyrimidine Derivatives." Journal of Drug Delivery and Therapeutics 10, no. 5 (2020): 358–61. http://dx.doi.org/10.22270/jddt.v10i5.4295.

Full text
Abstract:
Pyrimidine is an aromatic heterocyclic organic compound similar to pyridine. One of the three diazines (six-membered heterocyclics with two nitrogen atoms in the ring), it has the nitrogens at positions 1 and 3 in the ring. Pyrimidines are typically synthesized by the “Principal Synthesis” involving cyclization of beta-dicarbonyl compounds with N-C-N compounds. Reaction of the former with amidines to give 2-substituted pyrimidines, with urea to give 2-pyrimidiones, and guanidines to give 2-aminopyrimidines are typical. Pyrimidines can be prepared via the biginelli reaction. Many other methods
APA, Harvard, Vancouver, ISO, and other styles
2

Hossain, M. I., and M. M. H. Bhuiyan. "Synthesis and Antimicrobial Activities of Some New Thieno and Furopyrimidine Derivatives." Journal of Scientific Research 1, no. 2 (2009): 317–25. http://dx.doi.org/10.3329/jsr.v1i2.2299.

Full text
Abstract:
Fused pyrimidines, 8,9-dimethyl[1,2,4]triazolo[4,3-c]thieno[3,2-e]pyrimidine 5, 3,8,9-trimethyl[1,2,4]triazolo[4,3-c]thieno[3,2-e]pyrimidine 6, 4-benzylidinehydrazono-5,6 dimethylthieno[2,3-d]pyrimidine 7, 4-[4/-hydroxybenzylidine]hydrazono-5,6-dimethylthi-eno[2,3-d]pyrimidine 8, 4-[4/-tolylidin]hydrazono-5,6-dimethylthieno[2,3-d]pyrimidine 9, 4-[4/-nitrobenzylidine]hydrazono-5-ethyl-6-methylthieno[2,3-d]pyrimidine 10 and 4-[4/-chlorobenzylidine]hydrazono-5-ethyl-6-methylthieno[2,3-d]pyrimidine 11 are prepared in good yield by an initial treatment of 2-amino-4,5-dimethylthiophene-3-carbonitril
APA, Harvard, Vancouver, ISO, and other styles
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.

Full text
Abstract:
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
APA, Harvard, Vancouver, ISO, and other styles
4

Sirakanyan, Spinelli, Geronikaki, et al. "Synthesis, Antitumor Activity, and Docking Analysis of New Pyrido[3’,2’:4,5]furo(thieno)[3,2-d]pyrimidin-8-amines." Molecules 24, no. 21 (2019): 3952. http://dx.doi.org/10.3390/molecules24213952.

Full text
Abstract:
Continuing our research in the field of new heterocyclic compounds, herein we report on the synthesis and antitumor activity of new amino derivatives of pyrido[3’,2’:4,5](furo)thieno[3,2-d]pyrimidines as well as of two new heterocyclic systems: furo[2–e]imidazo[1,2-c]pyrimidine and furo[2,3-e]pyrimido[1,2-c]pyrimidine. Thus, by refluxing the 8-chloro derivatives of pyrido[3’,2’:4,5]thieno(furo)[3,2-d]pyrimidines with various amines, the relevant pyrido[3’,2’:4,5]thieno(furo)[3,2-d]pyrimidin-8-amines were obtained. Further, the cyclization of some amines under the action of phosphorus oxychlori
APA, Harvard, Vancouver, ISO, and other styles
5

Azam, Mohammed Afzal, Loganathan Dharanya, Charu Chandrakant Mehta, and Sumit Sachdeva. "Synthesis and biological evaluation of some novel pyrazolopyrimidines incorporating a benzothiazole ring system." Acta Pharmaceutica 63, no. 1 (2013): 19–30. http://dx.doi.org/10.2478/acph-2013-0001.

Full text
Abstract:
In the present study, a series of benzothiazol derivatives 3a-l containing pyrazolo[3,4-d]pyrimidine moiety at the second position were synthesized and characterized by analytical and spectral data. The compounds were tested for their in vitro antimicrobial activity. Compounds 1-(1,3-benzothiazol-2- yl)-3-methyl-4-phenyl-1H-pyrazolo[3,4-d]pyrimidine (3a), 1- (1,3-benzothiazol-2-yl)-4-(4-chlorophenyl)-3-methyl-1H-pyrazolo[ 3,4-d]pyrimidine (3d) and 1-(1,3-benzothiazol-2-yl)- 3-methyl-4-substituted phenyl-1H-pyrazolo[3,4-d]pyrimidines (3h-j) showed significant inhibitory activity against P. aeru
APA, Harvard, Vancouver, ISO, and other styles
6

Agarkov, Artem S., Dilyara O. Mingazhetdinova, Anna A. Nefedova, et al. "Synthesis and Structure of 6-Acetyl-2-Arylhydrazone Derivatives of Thiazolo[3,2-a]Pyrimidine." Organics 4, no. 3 (2023): 438–46. http://dx.doi.org/10.3390/org4030031.

Full text
Abstract:
Triazolo[4,3-a]pyrimidine is one of the promising structural fragments for the development of drugs, including anticancer drugs. This work is devoted to the synthesis of a number of new 2-arylhydrazone derivatives of thiazolo[3,2-a]pyrimidine, which are synthetic precursors for triazolo[4,3-a]pyrimidines. The crystal structure of 6-acetyl-7-methyl-5-phenyl-2-(2-phenylhydrazineylidene)-5H-thiazolo[3,2-a]pyrimidin-3(2H)-one was established by SCXRD. In the reduction reaction of the compound, the following system was used: vanadium(V) oxide, and sodium borohydride in ethanol at room temperature,
APA, Harvard, Vancouver, ISO, and other styles
7

Ho, Yuh-Wen, and Maw Cherng Suen. "Thioxopyrimidine in Heterocyclic Synthesis I: Synthesis of Some Novel 6-(Heteroatom-substituted)-(thio)pyrimidine Derivatives." Journal of Chemistry 2013 (2013): 1–15. http://dx.doi.org/10.1155/2013/765243.

Full text
Abstract:
A series of novel N-cycloalkanes, morpholine, piperazines, pyrazole, pyrimidine, benzimidazolo[1,2-a]pyrimidine, 1,2,3,4-tetrazolo[1,5-a]pyrimidine, azopyrazolo[1,5- a]pyrimidine, pyrimido[4', 5':3,4]pyrazolo[1,5-a]pyrimidines and pyridine derivatives incorporating a 5-cyano-4-methyl-2-phenyl-(thio)pyrimidine moiety were obtained by the intramolecular cyclization of 6-methylthio-pyrimidine, 6-(benzoylmethyl)thio- pyrimidine and 2-[(5-cyano-4-methyl-2-phenylpyrimidin-6-yl)thio]-3-dimethyl- amino-1-phenyl-prop-2-en-1-one with appropriate amines and enaminone compounds, respectively. The structur
APA, Harvard, Vancouver, ISO, and other styles
8

Mosaad, Sayed Mohamed, Mohamed Awad Samir, Abdallah Abd El-tawab Neama, and Mohamed Ahmed Naglaa. "An overview on synthesis and biological activity of pyrimidines." World Journal of Advanced Research and Reviews 15, no. 1 (2022): 272–96. https://doi.org/10.5281/zenodo.7743045.

Full text
Abstract:
Pyrimidines represent an important class of heterocycles containing two nitrogen atoms at position 1 and 3 of the six membered ring show wide range of biological activities. Numerous methods for the synthesis of pyrimidine and their diverse reactions offer enormous scope in the field of medicinal chemistry. Pyrimidine possesses wide spectrum of biological activities including antitubercular, antibacterial, antifungal, antiviral, anti-inflammatory, antimalarial, anticancer, and anti-HIV activity. The present review attempts to give brief information about the synthesis and various biological ac
APA, Harvard, Vancouver, ISO, and other styles
9

Mohammed, F. K., and M. G. Badrey. "Synthesis of Pyrimidines and Heteroannulated Pyrimidine Ring Systems." Journal of the Korean Chemical Society 55, no. 2 (2011): 218–29. http://dx.doi.org/10.5012/jkcs.2011.55.2.218.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Venugopala, Katharigatta N., and Vinuta Kamat. "Pyrimidines: A New Versatile Molecule in the Drug Development Field, Scope, and Future Aspects." Pharmaceuticals 17, no. 10 (2024): 1258. http://dx.doi.org/10.3390/ph17101258.

Full text
Abstract:
Pyrimidine is a moiety that occurs in living organisms and has a variety of significant biological properties in pharmacology. Due to the easy handling of synthesis, easily available precursor, and less duration for the reaction, for the synthesis, not many technical skills are needed. All these factors attract chemists to focus more on pyrimidines. Apart from the synthesis of biological applications of pyrimidines, medicinal chemists have gathered to explore more pyrimidine scaffolds due to their interesting medicinal properties and easy targeting of various binding sites. This review delves
APA, Harvard, Vancouver, ISO, and other styles
More sources

Dissertations / Theses on the topic "Pyrimidine synthesis"

1

Collins, James P. "Prebiotic Synthesis of Pyrimidine Nucleosides." Thesis, Georgia Institute of Technology, 2005. http://hdl.handle.net/1853/14095.

Full text
Abstract:
The problem of forming a glycosidic bond between ribose and the free nucleoside bases to produce beta-nucleosides under plausible prebiotic conditions is commonly referred to in origin of life research as The Nucleoside Problem. The lack of a general solution to this problem currently represents one of the largest stumbling blocks to the RNA world hypothesis and many other theories regarding the origin of life. Over thirty years ago the purine nucleosides were successfully synthesized by drying the fully-formed bases and ribose together in the presence of divalent metal ion salts. However, gly
APA, Harvard, Vancouver, ISO, and other styles
2

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
3

Hill, Matthew D. (Matthew Dennis). "Direct synthesis of pyridine and pyrimidine derivatives." Thesis, Massachusetts Institute of Technology, 2008. http://hdl.handle.net/1721.1/43776.

Full text
Abstract:
Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Chemistry, 2008.<br>Vita.<br>Includes bibliographical references.<br>I. Synthesis of Substituted Pyridine Derivatives via the Ruthenium-Catalyzed Cycloisomerization of 3-Azadienynes. The two-step conversion of various N-vinyl and N-aryl amides to the corresponding substituted pyridines and quinolines, respectively, is described. The process involves the direct conversion of amides, including sensitive N-vinyl amides, to the corresponding trimethylsilyl alkynyl imines followed by a ruthenium-catalyzed protodesilylation and cyclois
APA, Harvard, Vancouver, ISO, and other styles
4

Chan, Heng Ming. "Synthesis of pyrimidine C-nucleoside analogues and triphosphate derivatives." Thesis, Boston College, 2008. http://hdl.handle.net/2345/36.

Full text
Abstract:
Five pyrimidine C-nucleosides were prepared via Heck-type coupling reactions. These derivatives are designed to mimic dC and dU (or T). The minor groove O2 carbonyl in each derivative is replaced by a hydrogen, a fluorine, or a methyl group. The hydrogen-substituted dC analogue was converted into a 2’,3’-dideoxynucleoside, which was converted into a 5’-triphosphate derivative. The other two dC analogues were transformed into 5’-triphosphate derivatives immediately after Heck coupling reactions. These analogues will allow an examination of the nature and role of minor groove interactions betwee
APA, Harvard, Vancouver, ISO, and other styles
5

Sullivan, Shannon M. "Synthesis of 2,4-disubstituted pyrimidine derivatives as potential 5-HT7 receptor antagonist." unrestricted, 2008. http://etd.gsu.edu/theses/available/etd-05052008-153400/.

Full text
Abstract:
Thesis (M.S.)--Georgia State University, 2008.<br>Title from file title page. Lucjan Strekowski, committee chair; A.L. Baumstark, Gabor Patonay, Doyle Barrow , committee members. Electronic text (68 p. : ill.) : digital, PDF file. Description based on contents viewed June 23, 2008. Includes bibliographical references (p. 42-430.
APA, Harvard, Vancouver, ISO, and other styles
6

蘇雅頌 and Ngar-chung Nellie So. "Pyrimidine nucleotide biosynthesis in adult angiostrongylus Cantonensis (Nematoda : Metastrongyloidea)." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1993. http://hub.hku.hk/bib/B3123320X.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Taleli, Lebusetsa. "Radiosynthesis of various pyrimidine derivatives and determining their uptake into cells." Thesis, Cape Peninsula University of Technology, 2009. http://hdl.handle.net/20.500.11838/744.

Full text
Abstract:
Thesis (MTech (Chemistry))--Cape Peninsula University of Technology, 2009<br>N3-substituted pyrimidine nucleoside derivatives containing either an iodovinyl moiety or an allyl group, i.e. [121]-N3-(3-iodoprop-2-en- l -yl)thymidine, (1~-711 and e21]-N3-(prop-2-enl- yl)-5-iodo-Z'-deoxyuridine, (1~_10, were synthesised and preliminarily evaluated by determining their uptake into CHO-Kl cells. Compound e~-711 was designed to be a delivery vector of 121: into the DNA of the cells, while (1~_10 was designed to serve as a control. Compound (1231]-711 was also intended to have a higher metabolic
APA, Harvard, Vancouver, ISO, and other styles
8

McFadden, Helen Georgina, and n/a. "Synthesis and herbicidal properties of some pyrazole and pyrimidine heteocycles." University of Canberra. Biomedical Sciences, 1992. http://erl.canberra.edu.au./public/adt-AUC20060918.160845.

Full text
Abstract:
Four main series of novel heterocyclic compounds were successfully syniliesised. Two of these series were found to be post-emergence herbicides with the activities of each being based on a different mode of action. The (pyrazole-4-yl)alkanones are inhibitors of protoporphyrinogen oxidase, an enzyme in chlorophyll biosynthesis, whereas alkyl 3-arylsulfonylamino- 3-methyllhio-2-(pyrimidin-2-ylcarbamoyl)acrylates and pyrimidin-2-yl 3-(2- chlorophenyl)sulfonyl-amino-3-methylthio-2-cyanoacrylamides (collectively termed "vinylogous sulfonylureas") are inhibitors of acetohydroxy acid synthase (AHAS).
APA, Harvard, Vancouver, ISO, and other styles
9

Sūdžius, Jurgis. "Synthesis And Properties Of Pyrimidine Derivatives – Potent Carbonic Anhydrase Inhibitors." Doctoral thesis, Lithuanian Academic Libraries Network (LABT), 2011. http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2011~D_20110519_082332-05105.

Full text
Abstract:
The aim of the work was design of pyrimidine derivatives – potent carbonic anhydrase (CA) inhibitors. Theoretical investigation of interaction of 4-[N-(pyrimidin-4-yl)]aminobenzenesulfonamides containing substituents at 2-, 5- and 6- positions of pyrimidine ring with an active site of hCAs suggested that these compounds can fit into an active site of the enzymes and should interact with them as typical hCA inhibitors. Synthesis of target compounds was carried out by substitution of chloro group at 4,6-dichloropyrimidines containing cyano-, formyl- or nitro groups at position 5 of the pyrimidin
APA, Harvard, Vancouver, ISO, and other styles
10

Buntain, I. G. "The design, synthesis and testing of inhibitors of pyrimidine biosynthesis." Thesis, University of Strathclyde, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.372118.

Full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Books on the topic "Pyrimidine synthesis"

1

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

Find full text
APA, Harvard, Vancouver, ISO, and other styles
2

Mathur, Deepti. PTEN regulates glutamine flux to pyrimidine synthesis and sensitivity to dihydroorotate dehydrogenase inhibition. [publisher not identified], 2017.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
3

Wu, Xiao-Feng, and Zechao Wang. Transition Metal-Catalyzed Pyrimidine Synthesis: Transition Metal-Catalyzed Heterocycle Synthesis Series. Elsevier Science & Technology Books, 2016.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
4

Babu, B. Synthesis of Condensed Thiazolo-[3,2-a] Pyrimidine Systems. Routledge, 1991.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
5

Stebbins, Jeffrey W. Catalysis, regulation and relationship to structure of Escherichia coli aspartate transcarbamoylase: By Jeffrey William Stebbins. 1990.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
6

Wu, Xiao-Feng, and Zechao Wang. Transition Metal Catalyzed Pyrimidine, Pyrazine, Pyridazine and Triazine Synthesis: Transition Metal-Catalyzed Heterocycle Synthesis Series. Elsevier, 2016.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
7

Study of the Synthesis of 20-Trifluoromethyl Pyrimidines. Creative Media Partners, LLC, 2021.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
8

Frackenpohl, Carmen. Synthese neuer 5-arylsubstituierter Pyrrolo[2,3-d]pyrimidin-Derivate. 2000.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
9

Detmer, Monika. Zur Synthese dreikerniger Heterocyclen über neuartig substituierte Pyrido[2,3-d]pyrimidine. 2004.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
10

Cihák, A., and W. Reutter. Orotic Acid: Synthesis, Biochemical Aspects and Physiological Role. Springer, 2012.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Book chapters on the topic "Pyrimidine synthesis"

1

Kumar, Vipan, and Mohinder P. Mahajan. "Pyrimidine and Imidazole." In Heterocycles in Natural Product Synthesis. Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527634880.ch14.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Switzer, Robert L., and Cheryl L. Quinn. "De Novo Pyrimidine Nucleotide Synthesis." In Bacillus subtilis and Other Gram-Positive Bacteria. ASM Press, 2014. http://dx.doi.org/10.1128/9781555818388.ch25.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Ueda, Tohru. "Synthesis and Reaction of Pyrimidine Nucleosides." In Chemistry of Nucleosides and Nucleotides. Springer US, 1988. http://dx.doi.org/10.1007/978-1-4613-0995-6_1.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Kleschick, William A., Mark J. Costales, B. Clifford Gerwick, et al. "1,2,4-Triazolo[1,5-a]pyrimidine-2-sulfonanilide Herbicides." In Synthesis and Chemistry of Agrochemicals III. American Chemical Society, 1992. http://dx.doi.org/10.1021/bk-1992-0504.ch002.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Kleschick, William A., C. M. Carson, Mark J. Costales, et al. "1,2,4-Triazolo[1,5-a]pyrimidine-2-sulfonanilide Herbicides." In Synthesis and Chemistry of Agrochemicals III. American Chemical Society, 1992. http://dx.doi.org/10.1021/bk-1992-0504.ch003.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Gordon, Ross B., and Bryan T. Emmerson. "Inhibition of De Novo Purine Synthesis by Methylthioadenosine." In Purine and Pyrimidine Metabolism in Man V. Springer US, 1986. http://dx.doi.org/10.1007/978-1-4684-1248-2_102.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Rowe, Peter B., Sandra E. McEwen, and Annette Kalaizis. "Purine Nucleotide Synthesis in Cultured Rat Embryos Undergoing Organogenesis." In Purine and Pyrimidine Metabolism in Man V. Springer US, 1986. http://dx.doi.org/10.1007/978-1-4684-1248-2_84.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Snyder, Floyd F., Kuldeep Neote, Eddie Kwan, and Ellen R. Mably. "Synthesis and Turnover of Purine Nucleoside Phosphorylase in Human Lymphocytes." In Purine and Pyrimidine Metabolism in Man V. Springer US, 1986. http://dx.doi.org/10.1007/978-1-4684-1248-2_40.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Allison, A. C., T. Hovi, R. W. E. Watts, and A. D. B. Webster. "The Role ofde novoPurine Synthesis in Lymphocyte Transformation." In Ciba Foundation Symposium 48 - Purine and Pyrimidine Metabolism. John Wiley & Sons, Ltd., 2008. http://dx.doi.org/10.1002/9780470720301.ch13.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Joule, J. A., K. Mills, and G. F. Smith. "The diazines: pyridazine, pyrimidine and pyrazine: reactions and synthesis." In Heterocyclic Chemistry. Springer US, 1995. http://dx.doi.org/10.1007/978-1-4899-3222-8_11.

Full text
APA, Harvard, Vancouver, ISO, and other styles

Conference papers on the topic "Pyrimidine synthesis"

1

Simijonović, Dušica, Edina Avdović, Žiko Milanović, Dejan Milenković, and Zoran Marković. "Green synthesis of chromeno-pyrimidine derivatives – Part I." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.686s.

Full text
Abstract:
Two different chromeno-pyrimidine derivatives were synthetized in the ionic liquid catalyzed reaction of barbituric acid and substituted salicylaldehydes. The product 5-(7-bromo-2,4-dioxo-1,3,4,5-tetrahydro-2H-chromeno[2,3-d]pyrimidin-5-yl)pyrimidine-2,4,6(1H,3H,5H)-tri-one (CP-1) was obtained in the reaction of barbiruric acid and 5-bromo-2-hydroxybenzaldehyde. The second new product 8,9-dihydroxy-2H-chromeno[2,3-d]pyrimidine-2,4(3H)-dione (CP-2) was yielded in the reaction between barbituric acid and 2,3,4-trihydroxybenzaldehyde. These products were isolated in moderate to good yield after 3
APA, Harvard, Vancouver, ISO, and other styles
2

Xavier, Augusto L., Daniel S. Alexandrino, Emerson P. S. Falcão, Rajendra M. Srivastava, and Janaina V. dos Anjos. "A green, microwave-mediated, multicomponent synthesis of pyrimidine and pyrimidinone derivatives." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0024-1.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Scapin, Elisandra, Lilian Buriol, Taiana Scalco München, Clarissa Piccinin Frizzo, and Marcos A. P. Martins. "Synthesis of 1,2,4-Triazolo[1,5-a]pyrimidine Supported under Ultrasound Irradiation." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_20131012143813.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Shutalev, Anatoly, and Anastasia Fesenko. "Synthesis of 5-(diethoxyphosphoryl)-substituted Hydrogenated Pyrimidine-2-thiones." In The 11th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2007. http://dx.doi.org/10.3390/ecsoc-11-01328.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Scapin, Elisandra, Lilian Buriol, Taiana Scalco München, Clarissa Piccinin Frizzo, Mara Marzari, and Marcos A. P. Martins. "Synthesis of 7-aryl(alkyl)1,2,4-triazolo[1,5-a]pyrimidine Using Conventional Methods." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0028-1.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Ferreira, Marcelle de Souza, and José Daniel Figueroa Villar. "Synthesis of news furo[2,3-d] pyrimidine derivatives as potential inhibitors of DHFR." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013913121221.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Shutalev, Anatoly. "A New Approach to the Synthesis of Hydrogenated Pyrimidine-2-imines." In The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01854.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Gabitova, Elina, Artem Agarkov, Mariya Mailyan, et al. "Synthesis of Triazolyl Derivatives Based on Thiazolo[3,2-a]pyrimidine Propargyl Ethers." In ECSOC 2024. MDPI, 2024. https://doi.org/10.3390/ecsoc-28-20126.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Ridder, D., M. Schindeldecker, K. Berndt, et al. "Key enzymes in pyrimidine synthesis, CAD and CPS1, predict prognosis in hepatocellular carcinoma." In 37. Jahrestagung der Deutschen Arbeitsgemeinschaft zum Studium der Leber. Georg Thieme Verlag KG, 2021. http://dx.doi.org/10.1055/s-0040-1722067.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

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. MDPI, 2009. http://dx.doi.org/10.3390/ecsoc-13-00169.

Full text
APA, Harvard, Vancouver, ISO, and other styles
You might also be interested in the extended bibliographies on the topic 'Pyrimidine synthesis' for particular source types:
Journal articles Dissertations / Theses Books
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!

To the bibliography