Статті в журналах з теми "Pyrimidine ring"
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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 (September 15, 2020): 358–61. http://dx.doi.org/10.22270/jddt.v10i5.4295.
Повний текст джерелаWenska, Grazyna, Bohdan Skalski, Stefan Paszyc, and Zofia Gdaniec. "Photochemistry of N-(pyrimidin-2-one-4-yl)pyridinium derivatives. The ring contraction of pyrimidinone into imidazolinone." Canadian Journal of Chemistry 73, no. 12 (December 1, 1995): 2178–84. http://dx.doi.org/10.1139/v95-270.
Повний текст джерелаMohammed, F. K., and M. G. Badrey. "Synthesis of Pyrimidines and Heteroannulated Pyrimidine Ring Systems." Journal of the Korean Chemical Society 55, no. 2 (April 20, 2011): 218–29. http://dx.doi.org/10.5012/jkcs.2011.55.2.218.
Повний текст джерелаAzam, 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 (March 1, 2013): 19–30. http://dx.doi.org/10.2478/acph-2013-0001.
Повний текст джерелаGallagher, P. E., and N. J. Duker. "Detection of UV purine photoproducts in a defined sequence of human DNA." Molecular and Cellular Biology 6, no. 2 (February 1986): 707–9. http://dx.doi.org/10.1128/mcb.6.2.707-709.1986.
Повний текст джерелаGallagher, P. E., and N. J. Duker. "Detection of UV purine photoproducts in a defined sequence of human DNA." Molecular and Cellular Biology 6, no. 2 (February 1986): 707–9. http://dx.doi.org/10.1128/mcb.6.2.707.
Повний текст джерелаYamuna, Thammarse S., Jerry P. Jasinski, Brian J. Anderson, H. S. Yathirajan, and Manpreet Kaur. "4-Hydroxy-5-(2-methoxyphenoxy)-2,2′-bipyrimidin-6(5H)-one dihydrate." Acta Crystallographica Section E Structure Reports Online 69, no. 11 (October 26, 2013): o1707—o1708. http://dx.doi.org/10.1107/s1600536813028900.
Повний текст джерелаAhmed Elkanzi, Nadia Ali. "Synthesis and Biological Activities of Some Pyrimidine Derivatives: A Review." Oriental Journal Of Chemistry 36, no. 6 (December 30, 2020): 1001–15. http://dx.doi.org/10.13005/ojc/360602.
Повний текст джерелаBehera, Manoranjan, M. Sambaiah, Poosa Mallesham, K. Shiva Kumar, Yamini Bobde, Prasanta Hota, Satyanarayana Yennam, and Balaram Ghosh. "Tandem Schiff-Base Formation/Heterocyclization: An Approach to the Synthesis of Fused Pyrazolo–Pyrimidine/Isoxazolo-Pyrimidine Hybrids." Synlett 30, no. 05 (February 5, 2019): 586–92. http://dx.doi.org/10.1055/s-0037-1612081.
Повний текст джерелаHuppatz, JL. "Systemic Fungicides. The Synthesis of Pyrazolo[1,5-a]pyrimidine Analogues of Carboxin." Australian Journal of Chemistry 38, no. 1 (1985): 221. http://dx.doi.org/10.1071/ch9850221.
Повний текст джерелаNerkar, A. G., S. A. Ghone, and A. K. Thaker. "In SilicoScreening of the Library of Pyrimidine Derivatives as Thymidylate Synthase Inhibitors for Anticancer Activity." E-Journal of Chemistry 6, no. 3 (2009): 665–72. http://dx.doi.org/10.1155/2009/352717.
Повний текст джерелаMaji, Pradip Kumar. "Synthesis of Pyrimidine-Annulated Five-Membered Heterocycles: An Overview." Current Organic Chemistry 23, no. 20 (December 24, 2019): 2204–69. http://dx.doi.org/10.2174/1385272823666191019111627.
Повний текст джерелаMosaad Sayed Mohamed, Samir Mohamed Awad, Neama Abdallah Abd El-tawab, and Naglaa Mohamed Ahmed. "An overview on synthesis and biological activity of pyrimidines." World Journal of Advanced Research and Reviews 15, no. 1 (July 30, 2022): 272–96. http://dx.doi.org/10.30574/wjarr.2022.15.1.0689.
Повний текст джерелаJubete, Guillem, Raimon Puig de la Bellacasa, Roger Estrada-Tejedor, Jordi Teixidó, and José I. Borrell. "Pyrido[2,3-d]pyrimidin-7(8H)-ones: Synthesis and Biomedical Applications." Molecules 24, no. 22 (November 16, 2019): 4161. http://dx.doi.org/10.3390/molecules24224161.
Повний текст джерелаCawrse, Brian M., Nia’mani M. Robinson, Nina C. Lee, Gerald M. Wilson, and Katherine L. Seley-Radtke. "Structural and Biological Investigations for a Series of N-5 Substituted Pyrrolo[3,2-d]pyrimidines as Potential Anti-Cancer Therapeutics." Molecules 24, no. 14 (July 23, 2019): 2656. http://dx.doi.org/10.3390/molecules24142656.
Повний текст джерелаBischoff, Kerstin, Ulrich Girreser, Dieter Heber, and Martin Schütt. "Two-Step Synthetic Approach to 6-Substituted Pyrido[2,3-d]pyrimidine(1H,3H)-2,4-diones from 6-Amino-, 6-Alkylamino-, and 6-Arylamino-1,3-dimethyluracils." Zeitschrift für Naturforschung B 61, no. 4 (April 1, 2006): 486–94. http://dx.doi.org/10.1515/znb-2006-0415.
Повний текст джерелаKang, Gihaeng, Jineun Kim, Hyunjin Park, and Tae Ho Kim. "Crystal structure of nuarimol." Acta Crystallographica Section E Crystallographic Communications 71, no. 8 (July 22, 2015): o586—o587. http://dx.doi.org/10.1107/s2056989015013493.
Повний текст джерелаBommagani, Shobanbabu, Narsimha R. Penthala, Sean Parkin, and Peter A. Crooks. "Crystal structure of (E)-13-(pyrimidin-5-yl)parthenolide." Acta Crystallographica Section E Crystallographic Communications 71, no. 12 (November 28, 2015): 1536–38. http://dx.doi.org/10.1107/s2056989015021507.
Повний текст джерелаZhang, Zheng-Hong, Xiao-Ling Liu, and Long-Ju Chen. "2-(2-Hydroxyethylamino)-3-phenyl-1-benzofuro[3,2-d]pyrimidin-4(3H)-one dichloromethane hemisolvate." Acta Crystallographica Section E Structure Reports Online 65, no. 6 (May 20, 2009): o1330. http://dx.doi.org/10.1107/s1600536809017814.
Повний текст джерелаBernhardt, Paul V., and Curt Wentrup. "Structures of 4-Iminopyrido[1,2-a]pyrimidines, Pyrido[1,2-a]pyrimidin-4-ones, Pyridopyrimidinium Olates, and Thiazolo[3,2-a]pyrimidine Analogues." Australian Journal of Chemistry 65, no. 4 (2012): 371. http://dx.doi.org/10.1071/ch12040.
Повний текст джерелаMaccabee, Margaret, Janet S. Evans, Mary P. Glackin, Zafer Hatahet, and Susan S. Wallace. "Pyrimidine Ring Fragmentation Products." Journal of Molecular Biology 236, no. 2 (February 1994): 514–30. http://dx.doi.org/10.1006/jmbi.1994.1162.
Повний текст джерелаMonier, Mohamed, Doaa Abdel-Latif, Ahmed El-Mekabaty, Başak D. Mert, and Khaled M. Elattar. "Advances in the Chemistry of 6-6 Bicyclic Systems: Chemistry of Pyrido[3,4- d]pyrimidines." Current Organic Synthesis 16, no. 6 (November 26, 2019): 812–54. http://dx.doi.org/10.2174/1570179416666190704113647.
Повний текст джерелаSankar, T., S. Naveen, N. K. Lokanath, and K. Gunasekaran. "Crystal structure of ethyl 4-(2,4-dichlorophenyl)-2-methyl-4H-benzo[4,5]thiazolo[3,2-a]pyrimidine-3-carboxylate." Acta Crystallographica Section E Crystallographic Communications 71, no. 5 (April 15, 2015): o306—o307. http://dx.doi.org/10.1107/s2056989015007033.
Повний текст джерелаChaudhary, Ankita. "Multicomponent Approach for the Sustainable Syntheses of Pyrido[2,3-d]pyrimidine Scaffold." Current Organic Chemistry 25, no. 23 (December 16, 2021): 2856–84. http://dx.doi.org/10.2174/1385272825666211117152900.
Повний текст джерелаHordiyenko, Olga V., Volodymyr A. Tkachuk, Vyacheslav O. Shishkanu, Tetiana M. Tkachuk, and Svitlana V. Shishkina. "2-Carbamimidoylbenzoic Acid as a New Effective and Available Precursor for the Synthesis of Substituted 2-(Pyrimidin-2-yl)benzoic Acids." Synthesis 53, no. 02 (November 16, 2020): 371–82. http://dx.doi.org/10.1055/s-0040-1705941.
Повний текст джерелаKordian, Marcus, Holger Feist, and Klaus Peseke. "Anellation and Ring Transformations of Push-pull-functionalized Deoxypyranosiduloses." Zeitschrift für Naturforschung B 64, no. 6 (June 1, 2009): 676–82. http://dx.doi.org/10.1515/znb-2009-0613.
Повний текст джерелаKant, Rajni, Vivek K. Gupta, Kamini Kapoor, S. Samshuddin, and B. Narayana. "2-[3,5-Bis(4-methoxyphenyl)-4,5-dihydro-1H-pyrazol-1-yl]-4,6-bis(4-methoxyphenyl)pyrimidine." Acta Crystallographica Section E Structure Reports Online 68, no. 8 (July 10, 2012): o2398. http://dx.doi.org/10.1107/s1600536812030516.
Повний текст джерелаAbdelhamid, Ismail A., Amr M. Abdelmoniem, Farid M. Sroor, Muhammed A. Ramadan, and Said A. S. Ghozlan. "Hantzsch-Like One-Pot Three-Component Synthesis of Heptaazadicyclopenta[a,j]anthracenes: A New Ring System." Synlett 31, no. 09 (March 17, 2020): 895–98. http://dx.doi.org/10.1055/s-0040-1708001.
Повний текст джерелаSankar, T., S. Naveen, N. K. Lokanath, and K. Gunasekaran. "Crystal structure of (2-methyl-4-phenyl-4H-benzo[4,5]thiazolo[3,2-a]pyrimidin-3-yl)(phenyl)methanone." Acta Crystallographica Section E Crystallographic Communications 71, no. 5 (April 2, 2015): o276—o277. http://dx.doi.org/10.1107/s2056989015006428.
Повний текст джерелаSharma, Naresh, Goutam Brahmachari, Suvankar Das, Rajni Kant, and Vivek K. Gupta. "2-[4-(Piperidin-1-yl)-5H-chromeno[2,3-d]pyrimidin-2-yl]phenol." Acta Crystallographica Section E Structure Reports Online 70, no. 4 (March 15, 2014): o447—o448. http://dx.doi.org/10.1107/s1600536814005625.
Повний текст джерелаJung, Eunkyung, Ruben Soto-Acosta, Robert J. Geraghty, and Liqiang Chen. "Zika Virus Inhibitors Based on a 1,3-Disubstituted 1H-Pyrazolo[3,4-d]pyrimidine-amine Scaffold." Molecules 27, no. 18 (September 19, 2022): 6109. http://dx.doi.org/10.3390/molecules27186109.
Повний текст джерелаSoni, Hetal I., and Navin B. Patel. "PYRIMIDINE INCORPORATED SCHIFF BASE OF ISONIAZID WITH THEIR SYNTHESIS, CHARACTERIZATION AND IN VITRO BIOLOGICAL EVALUATION." Asian Journal of Pharmaceutical and Clinical Research 10, no. 10 (September 1, 2017): 209. http://dx.doi.org/10.22159/ajpcr.2017.v10i10.19302.
Повний текст джерелаJournal, Baghdad Science. "Synthesis of Some Heterocyclic Compounds derived from 2-mercapto pyrimidine." Baghdad Science Journal 7, no. 2 (June 6, 2010): 1014–22. http://dx.doi.org/10.21123/bsj.7.2.1014-1022.
Повний текст джерелаMoyaert, Tristen E., Christina Paul, Weibin Chen, Amy A. Sarjeant, and Louise N. Dawe. "Aquachlorido(2-{[6-(dimethylamino)pyrimidin-4-yl]sulfanyl}pyrimidine-4,6-diamine)copper(II) chloride hydrate." Acta Crystallographica Section E Crystallographic Communications 73, no. 10 (September 25, 2017): 1534–38. http://dx.doi.org/10.1107/s205698901701338x.
Повний текст джерелаMahesha, Ninganayaka, Hemmige S. Yathirajan, Tetsundo Furuya, Takashiro Akitsu та Christopher Glidewell. "The crystal structure of 1-(2-iodobenzoyl)-4-(pyrimidin-2-yl)piperazine: a three-dimensional hydrogen-bonded framework, augmented by π–π stacking interactions and I...N halogen bonds". Acta Crystallographica Section E Crystallographic Communications 75, № 2 (4 січня 2019): 129–33. http://dx.doi.org/10.1107/s205698901801811x.
Повний текст джерелаZeng, Qing, Demin Ren, Aiting Zheng, and Xiaofang Li. "Synthesis of Octahydropyrano[2,3-d]Pyrimidine Derivatives via Tetrahydropyrano[3,2-e][1,3]Thiazolo[3,2-a]Pyrimidine and 2,6-Dichlorobenzonitrile Oxide." Journal of Chemical Research 42, no. 6 (June 2018): 317–19. http://dx.doi.org/10.3184/174751918x15293130141511.
Повний текст джерелаLi, Hong-Xia, Yu-Su Song, Yong-nian Qu, Jiang-Bing Lu, and Hong-Mei Wang. "Ethyl 2-methyl-6-(propan-2-ylamino)-4-sulfanylidene-3H,11H-pyrimido[1,6-c]quinazoline-1-carboxylate." Acta Crystallographica Section E Structure Reports Online 68, no. 6 (May 19, 2012): o1821. http://dx.doi.org/10.1107/s1600536812019952.
Повний текст джерелаWolska, Irena, and Franciszek Herold. "Crystal and Molecular Structure of 4-Arylhexahydro-1H,3H-pyrido[1,2-c]pyrimidine-1,3-dione Derivatives." Zeitschrift für Naturforschung B 57, no. 11 (November 1, 2002): 1315–19. http://dx.doi.org/10.1515/znb-2002-1118.
Повний текст джерелаWei, Xia, and Xieraili Maimaitiyiming. "Enrichment of highly pure large-diameter semiconducting SWCNTs by polyfluorene-containing pyrimidine ring." RSC Advances 9, no. 56 (2019): 32753–58. http://dx.doi.org/10.1039/c9ra06819h.
Повний текст джерелаSwinton Darious, Robert, Packianathan Thomas Muthiah, and Franc Perdih. "Supramolecular architectures in the salt trimethoprimium ferrocene-1-carboxylate and the cocrystal 4-amino-5-chloro-2,6-dimethylpyrimidine–ferrocene-1-carboxylic acid (1/1)." Acta Crystallographica Section C Structural Chemistry 73, no. 9 (August 18, 2017): 743–48. http://dx.doi.org/10.1107/s2053229617011913.
Повний текст джерелаKokorekin, Vladimir A., Sergey V. Neverov, Vera N. Kuzina, and Vladimir A. Petrosyan. "A New Method for the Synthesis of 3-Thiocyanatopyrazolo[1,5-a]pyrimidines." Molecules 25, no. 18 (September 11, 2020): 4169. http://dx.doi.org/10.3390/molecules25184169.
Повний текст джерелаWolska, Irena, and Franciszek Herold. "Structural Investigation of Two 4-AryIhexahydro-1H,3H-pyrido[1,2-c]pyrimidine-1,3-diones." Zeitschrift für Naturforschung B 55, no. 11 (November 1, 2000): 1089–94. http://dx.doi.org/10.1515/znb-2000-1116.
Повний текст джерелаDelia, Thomas J., and Robin J. Hood. "Bromination of Pyrimidines: A Simple Inexpensive Method." Australian Journal of Chemistry 68, no. 2 (2015): 254. http://dx.doi.org/10.1071/ch14416.
Повний текст джерелаChmiel-Szukiewicz, Elżbieta. "Polyurethane foams with 1,3-pyrimidine ring." Journal of Applied Polymer Science 109, no. 3 (2008): 1708–13. http://dx.doi.org/10.1002/app.27159.
Повний текст джерелаTomlinson, Patricia Tolson, and Carol J. Lovatt. "Nucleotide Metabolism in ‘Washington’ Navel Orange Fruit: I. Pathways of Synthesis and Catabolism." Journal of the American Society for Horticultural Science 112, no. 3 (May 1987): 529–35. http://dx.doi.org/10.21273/jashs.112.3.529.
Повний текст джерелаFarghaly, Ahmed M., Ola H. Rizk, Inas Darwish, Manal Hamza, Mezna Saleh Altowyan, Assem Barakat, and Mohamed Teleb. "Design, Synthesis, Pharmacodynamic and In Silico Pharmacokinetic Evaluation of Some Novel Biginelli-Derived Pyrimidines and Fused Pyrimidines as Calcium Channel Blockers." Molecules 27, no. 7 (March 30, 2022): 2240. http://dx.doi.org/10.3390/molecules27072240.
Повний текст джерелаYu, Wang, Jingbao Song, and Aijian Wang. "Crystal structure of 4,6-bis[(E)-4-bromostyryl]-2-(butylsulfanyl)pyrimidine." Acta Crystallographica Section E Structure Reports Online 70, no. 12 (November 21, 2014): o1282. http://dx.doi.org/10.1107/s1600536814024714.
Повний текст джерелаAcosta, Lina M., Andrés F. Yepes, Alirio Palma, Justo Cobo, and Christopher Glidewell. "Six closely related 4,6-disubstituted 2-amino-5-formylpyrimidines: different ring conformations, polarized electronic structures, and hydrogen-bonded assembly in zero, one, two and three dimensions." Acta Crystallographica Section C Crystal Structure Communications 69, no. 2 (January 8, 2013): 162–71. http://dx.doi.org/10.1107/s0108270112051049.
Повний текст джерелаKrishnamurthy, M. S., and Noor Shahina Begum. "Crystal structure of methyl 4-(2-fluorophenyl)-6-methyl-2-sulfanylidene-1,2,3,4-tetrahydropyrimidine-5-carboxylate." Acta Crystallographica Section E Crystallographic Communications 71, no. 11 (October 14, 2015): o838—o839. http://dx.doi.org/10.1107/s2056989015018873.
Повний текст джерелаDevidas, Amrutkar Rakesh, Amrute Bhavesh Bharat, Ahire Ashishkumar Harishchndra, and Ziyaul Haque s. Ahmed. "IN SILICO ADMET PROFILING AND MOLECULAR DOCKING OF NOVEL SUBSTITUTED THIENO[3,2-d] PYRIMIDINES AGAINST LIGAND BINDING DOMAIN OF THE HUMAN PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR GAMMA IN COMPLEX WITH SYNTHETIC AGONIST." International Research Journal of Pharmacy 11, no. 11 (November 30, 2020): 36–40. http://dx.doi.org/10.7897/2230-8407.111195.
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