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Journal articles on the topic '3-5'

Author: Grafiati

Published: 4 June 2021

Last updated: 26 July 2025

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1

Halytskiy, V. A., and S. V. Komisarenko. "5'-CG-3', 5'-CNG-3', 5'-GC-3' and 5'-GNC-3' site localization in microRNA sequences." Biopolymers and Cell 27, no. 6 (2011): 499–505. http://dx.doi.org/10.7124/bc.00011c.

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2

V., K. Rao. "Synthesis of 4-(5-keto-2-phenyloxazolin-4-ylmethylene)-3-phenylisoxazol-5-one." Journal of Indian Chemical Society Vol. 83, Jan 2006 (2006): 87–88. https://doi.org/10.5281/zenodo.5816494.

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Division of Plant Physiology & Biochemistry, Indian Institute of Horticultural Research. Hessaraghatta. Bangalore-560 089, India <em>E-mail</em> : vkr5@yahoo.com <em>Manuscript received 29 June 2001. revised 4 July 2005. accepted 9 September 2005</em> 3-Phenylisoxazol-5-one (1) reacts with hippuric acid and ethyl orthoformate in acetic anhydride to give 4-(5- keto-2-phenyloxazolin-4-ylmethylene)-3-phenylisoxazol-5-one (4) in a single step.

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3

Chhakra, Sandhya, and S. . S. Chauhan. "SYNTHESIS OF NOVEL 4-(4-METHOXYBENZENE SULPHONYL)-3, 5-DIMETHYL/3-METHYL-5-PHENYL/3, 5- DIPHENYL/3, 5-DIMETHYL-1-PHENYL/3- METHYL -1, 5- DIPHENYL /1, 3, 5-TRIPHENYL PYRAZOLE." Rasayan Journal of Chemistry 12, no. 1 (2019): 290–93. http://dx.doi.org/10.31788/rjc.2019.1215030.

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4

Hiebl, Johann, Erich Zbiral, Jan Balzarini, and Erik De Clercq. "Synthesis and antiretrovirus properties of 5'-isocyano-5'-deoxythymidine,5'-isocyano-2',5'-dideoxyuridine,3'-azido-5'-isocyano-3',5'-dideoxythymidine, and 3'-azido-5'-isocyano-2',3',5'-trideoxyuridine." Journal of Medicinal Chemistry 34, no. 4 (1991): 1426–30. http://dx.doi.org/10.1021/jm00108a028.

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5

HIEBL, J., E. ZBIRAL, J. BALZARINI, and E. DE CLERCQ. "ChemInform Abstract: Synthesis and Antiretrovirus Properties of 5′-Isocyano-5′- deoxythymidine, 5′-Isocyano-2′,5′-dideoxyuridine, 3′-Azido-5′-isocyano- 3′,5′-dideoxythymidine, and 3′-Azido-5′-isocyano-2′,3′,5′- trideoxyuridine." ChemInform 22, no. 44 (2010): no. http://dx.doi.org/10.1002/chin.199144294.

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6

Kumar, S. Madan. "Nucleophilic Substitution on 5-Nitrobenzofurazan-3-Oxide: A New Synthetic Route for Novel Benzofurazan-5, 5′-Oxybis 3, 3′-Dioxide and Benzofurazan-5, 5′-Thiobis-3, 3′-Dioxide." Synthetic Communications 22, no. 5 (1992): 793–802. http://dx.doi.org/10.1080/00397919208019282.

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7

Ahabchane, Noureddine Hammou, Joseph Téné Ghomsi, and El Mokhtar Essassi. "(3(5) Phenylpyrazol-5(3)-yl)-2-benzoylmethyl Benzimidazole." Molecules 6, no. 6 (2001): M231. http://dx.doi.org/10.3390/m231.

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8

Liu, Xiaohai, and Colin B. Reese. "3′- Thiouridylyl - (3′→5′) - uridine." Tetrahedron Letters 37, no. 6 (1996): 925–28. http://dx.doi.org/10.1016/0040-4039(95)02281-3.

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9

Engler, Thomas A., Cynthia M. Scheibe, and Rajesh Iyengar. "Tandem 5 + 2/3 + 2 and 5 + 2/3 + 3 Cycloaddition Reactions." Journal of Organic Chemistry 62, no. 24 (1997): 8274–75. http://dx.doi.org/10.1021/jo971601k.

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10

Mitchell, Douglas W. "92.50 The 2:3:4, 3:4:5, 4:5:6 and 3:5:7 triangles." Mathematical Gazette 92, no. 524 (2008): 317–19. http://dx.doi.org/10.1017/s0025557200183299.

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11

Vinoo, Cameron. "-3 As the created root of all mathematics by numbers, Prime number 5 as the created template of all Prime number and pseudo-prime numbers(Mathematical Proof)." Journal of Progressive Research in Mathematics 14, no. 1 (2018): 2318–23. https://doi.org/10.5281/zenodo.3981236.

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The author has published several papers with JPRM which were unorthodox, but led to the acceptance of a major book on created mathematics , this small paper validates JPRM, and is a challenge to the entire current numbers theory if understood correctly .This small paper is the basic proof of the base of numbers in the created mathematics of the cone of Pythagoras 1:3 as Published at JPRM  , with the spiral arrangement of the Prime numbers and their multiples by the template of prime number 5, as the basis as shown separately in an upcoming book on created mathematics. The table entered in

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12

Meloni, Maria, Silvia Fanti, Daniele Tedesco, et al. "Characterization of chloroplast ribulose-5-phosphate-3-epimerase from the microalga Chlamydomonas reinhardtii." Plant Physiology 194, no. 4 (2023): 2263–77. https://doi.org/10.1093/plphys/kiad680.

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<em>This is a pre-copyedited, author-produced version of an article accepted for publication in Plant Physiology following peer review. The version of record [Maria Meloni, Silvia Fanti, Daniele Tedesco, Libero Gurrieri, Paolo Trost, Simona Fermani, Stéphane D. Lemaire, Mirko Zaffagnini, Julien Henri, Characterization of chloroplast ribulose-5-phosphate-3-epimerase from the microalga Chlamydomonas reinhardtii, Plant Physiology, Volume 194, Issue 4, April 2024, Pages 2263–2277] is available online at: https://academic.oup.com/plphys/article/194/4/2263/7491446 [DOI: 10.1093/plphys/k

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13

Hill, M., M. F. Mahon, and K. C. Molloy. "The Structure of 1, 5-Diazido-1, 1, 3, 3, 5, 5- hexabutyltristannoxane." Main Group Chemistry 1, no. 3 (1996): 309–15. http://dx.doi.org/10.1080/13583149612331338597.

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14

Glemarec, C., Á. Nyilas, C. Sund, and J. Chattopadhyaya. "A comparative conformational study of thymidylyl(3′ → 5′)-thymidine, thymidylyl(3′ → 5′)-5′-thio-5′-deoxythymidine and thymidinylacetomido-[3′(O) →′ (C)]-5′-deoxythymidine." Journal of Biochemical and Biophysical Methods 21, no. 4 (1990): 311–32. http://dx.doi.org/10.1016/0165-022x(90)90006-x.

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15

Plessis, Elise. "5 + 8 = 3." Mémoires N° 71, no. 3 (2017): 19. http://dx.doi.org/10.3917/mem.071.0019.

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16

Winker, MA, and LE Ferris. "Editorial 5(3)." Journal of Enam Medical College 5, no. 3 (2015): 134. http://dx.doi.org/10.3329/jemc.v5i3.24743.

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17

Pound, Linda. "Music 3 – 5." Music Education Research 12, no. 1 (2010): 122–24. http://dx.doi.org/10.1080/14613800903569260.

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18

Sharko, Anastasiya V., Ganna A. Senchyk, Eduard B. Rusanov, and Konstantin V. Domasevitch. "Preparative synthesis of 3(5),3′(5′)-dimethyl-4,4′-bipyrazole." Tetrahedron Letters 56, no. 44 (2015): 6089–92. http://dx.doi.org/10.1016/j.tetlet.2015.09.072.

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19

Scott, K. R., Ray J. Butcher, and Clive D. Hanson. "5-Methyl-3-(5-methylisoxazol-3-yl)cyclohex-2-enone." Acta Crystallographica Section E Structure Reports Online 62, no. 1 (2005): o215—o217. http://dx.doi.org/10.1107/s1600536805040766.

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20

Proni, Gloria, Gian Piero Spada, Giovanni Gottarelli, Federica Ciuchi, and Paolo Mariani. "Self-assembly of dideoxyguanosine (3?,3?) and (5?,5?)-monophosphates." Chirality 10, no. 8 (1998): 734–41. http://dx.doi.org/10.1002/(sici)1520-636x(1998)10:8<734::aid-chir3>3.0.co;2-n.

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21

Zelenin, K. N., I. P. Bezhan, and I. V. Lagoda. "5(3)-Hydroxyisoxazolidin-3(5)-ones and 5-hydroxy-pyrazolidin-3-ones and their ring-chain tautomerism." Chemistry of Heterocyclic Compounds 27, no. 2 (1991): 232–33. http://dx.doi.org/10.1007/bf00476765.

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22

Wen, Li-Rong, Jian-Xia Zhou, and Peng Liu. "5-Phenyl-3-[3-(5-phenyl-1,2,4-triazin-3-ylsulfanyl)propylsulfanyl]-1,2,4-triazine." Acta Crystallographica Section E Structure Reports Online 62, no. 10 (2006): o4704—o4705. http://dx.doi.org/10.1107/s1600536806038682.

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23

Lavandera, Iván, Susana Fernández, Miguel Ferrero, and Vicente Gotor. "Novel and efficient syntheses of 3′,5′-diamino derivatives of 2′,3′,5′-trideoxycytidine and 2′,3′,5′-trideoxyadenosine. Protonation behavior of 3′,5′-diaminonucleosides." Tetrahedron 59, no. 29 (2003): 5449–56. http://dx.doi.org/10.1016/s0040-4020(03)00870-6.

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24

Fu, Junhong, Michael D. Randles, Graeme J. Moxey, Rob Stranger, Marie P. Cifuentes та Mark G. Humphrey. "Mixed-metal cluster chemistry. 39. Syntheses and X-ray structures of Mo 3 Ir 3 (μ 4 -η 2 -CO)(μ 3 -CO)(CO) 10 (η 5 -C 5 H 5 ) 3 and Mo 3 RhIr 3 (μ-CO) 4 (CO) 7 (η 5 -C 5 H 5 ) 3 (η 5 -C 5 Me 5 )". Journal of Organometallic Chemistry 829 (лютий 2017): 66–70. http://dx.doi.org/10.1016/j.jorganchem.2016.10.016.

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25

Fu, Junhong, Graeme J. Moxey, Marie P. Cifuentes та Mark G. Humphrey. "Mixed-metal cluster chemistry. 35. Syntheses and structural studies of Mo 3 Ir 3 (μ 3 -O)(μ-CO) 3 (CO) 8 ( η 5 -C 5 H 5 ) 3 , Mo 4 Ir 4 (μ-CO) 4 (CO) 9 ( η 5 -C 5 H 5 ) 4 and Mo 3 Ir 5 (μ-CO) 3 (Cl)(CO) 6 ( η 5 -C 5 H 5 ) 3 ( η 5 -C 5 HMe 4 )". Journal of Organometallic Chemistry 792 (вересень 2015): 46–50. http://dx.doi.org/10.1016/j.jorganchem.2015.01.002.

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26

ZELENIN, K. N., I. P. BEZHAN, and I. V. LAGODA. "ChemInform Abstract: 5(3)-Hydroxy-3(5)-isoxazolidinones and 5-Hydroxy-3-pyrazolidinones and Their Ring-Chain Tautomerism." ChemInform 23, no. 8 (2010): no. http://dx.doi.org/10.1002/chin.199208206.

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27

Subramanyam, M., A. Thiruvalluvar, R. T. Sabapathy Mohan, and S. Kamatchi. "3-Cyano-3-methyl-5-phenylcyclohexanone." Acta Crystallographica Section E Structure Reports Online 63, no. 5 (2007): o2715—o2716. http://dx.doi.org/10.1107/s1600536807014055.

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28

Zhang, Zhenfeng, Shuo Jin, Siqian Wang, Bo Liu, and Jianping Guo. "3-Methyl-3-pyrazolin-5-one." Acta Crystallographica Section E Structure Reports Online 60, no. 2 (2004): o315—o316. http://dx.doi.org/10.1107/s160053680302974x.

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29

Nyilas, A., A. Földesi та J. Chattopadhyaya. "Synthesis of Cytidylyl(3′→5′)cytidylyl(3′→5′)-(2′)3′-O-[Lα-alanyl]adenosine". Nucleosides and Nucleotides 8, № 4 (1989): 557–67. http://dx.doi.org/10.1080/07328318908054198.

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30

ENGLER, T. A., C. M. SCHEIBE, and R. IYENGAR. "ChemInform Abstract: Tandem [5 + 2]/[3 + 2] and [5 + 2]/[3 + 3] Cycloaddition Reactions." ChemInform 29, no. 27 (2010): no. http://dx.doi.org/10.1002/chin.199827031.

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31

Fluck, Ekkehard, Manfred Spahn, and Gernot Heckmann. "Die Hydrolyse des 1, 1, 3, 3-Tetrakis(dimethylamino)-1?5, 3?5-diphosphets." Zeitschrift f�r anorganische und allgemeine Chemie 601, no. 1 (1991): 65–72. http://dx.doi.org/10.1002/zaac.19916010108.

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32

Ermolenko, Mikhail S., Sandrine Guillou, and Yves L. Janin. "Pyrazole-3/5-carboxylic acids from 3/5-trifluoromethyl NH-pyrazoles." Tetrahedron 69, no. 1 (2013): 257–63. http://dx.doi.org/10.1016/j.tet.2012.10.034.

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33

Lin, Jinlai, Kaizhang He, and Barbara Ramsay Shaw. "Novel 3‘,5‘-Cyclic Nucleotide Analogue: Adenosine 3‘,5‘-Cyclic Boranomonophosphate." Organic Letters 3, no. 6 (2001): 795–97. http://dx.doi.org/10.1021/ol0003230.

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34

Schäfer, H., and K. Gewald. "5-Arylamino-3-brom-1,2,4-thiadiazole und 5-Arylamino-3-bromisothiazole." Journal für Praktische Chemie 329, no. 2 (1987): 355–58. http://dx.doi.org/10.1002/prac.19873290230.

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35

Ueda, Kenta, Tsuyoshi Maeda, and Takahiro Wada. "Crystallographic and optical properties of CuGa 3 S 5 , CuGa 3 Se 5 and CuIn 3 (S,Se) 5 and CuGa 3 (S,Se) 5 systems." Thin Solid Films 633 (July 2017): 23–30. http://dx.doi.org/10.1016/j.tsf.2017.01.036.

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36

CHEUNG, TAK-MING, DEREK HORTON, WALDEMAR PRIEBE, WILLIAM R. TURNER, and WOLFGANG WECKERLE. "Sugar-ring analogs of daunorubicin: 3'-Epidaunorubicin, 3'-hydroxy-3',5'-diepidaunorubicin and 3',6'-dihydroxy-3',5'-diepidaunorubicin." Journal of Antibiotics 38, no. 5 (1985): 683–86. http://dx.doi.org/10.7164/antibiotics.38.683.

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37

Samano, Vicente, and Morris J. Robins. "Synthesis of 3′-deoxyadenosine-3′-spirocyclopropane, 3′-deoxy-uridine-3′-spirocyclopropane, and 5′-deoxy-4′,5′-methanoadenosine." Tetrahedron Letters 35, no. 21 (1994): 3445–48. http://dx.doi.org/10.1016/s0040-4039(00)73206-0.

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38

Brinek, Josef, Milan Alberti, Jaromir Marek, Zdirad Zak, and Jiri Touzin. "The reaction of P 3 N 3 Cl 5 NH 2 with SOCl 2 : the crystal structures of P 3 N 3 Cl 5 NSO and Cl 5 N 3 P 3 OP 3 N 3 Cl 5." Polyhedron 17, no. 18 (1998): 3235–41. http://dx.doi.org/10.1016/s0277-5387(98)00228-9.

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39

Editors, QRE. "Full Issue 5(3)." Qualitative Research in Education 5, no. 3 (2016): 229. http://dx.doi.org/10.17583/qre.2016.2369.

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40

Khan, Md Aminul Haque, and Rukhsana Parvin. "College News 5(3)." Journal of Enam Medical College 5, no. 3 (2015): 185. http://dx.doi.org/10.3329/jemc.v5i3.24755.

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41

Shevelev, Igor V., and Ulrich Hübscher. "The 3′–5′ exonucleases." Nature Reviews Molecular Cell Biology 3, no. 5 (2002): 364–76. http://dx.doi.org/10.1038/nrm804.

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42

Meifr, John P. "Matthew 5:3–12." Interpretation: A Journal of Bible and Theology 44, no. 3 (1990): 281–85. http://dx.doi.org/10.1177/002096430004400307.

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43

Maclean, Jennifer K. Berenson. "Micah 3:5-12." Interpretation: A Journal of Bible and Theology 56, no. 4 (2002): 413–16. http://dx.doi.org/10.1177/002096430005600408.

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44

Vernotte, Chabha. "3/5 Didier Anzieu." Soins Psychiatrie 36, no. 299 (2015): 45–46. http://dx.doi.org/10.1016/j.spsy.2015.04.012.

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45

Rivallan, Armel. "3/5 Guillaume Ferrus." Soins Psychiatrie 38, no. 311 (2017): 45–46. http://dx.doi.org/10.1016/j.spsy.2017.04.013.

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46

Matsuoka, Takeshi. "3-2-5 Videotex." Journal of the Institute of Television Engineers of Japan 39, no. 1 (1985): 82–83. http://dx.doi.org/10.3169/itej1978.39.82.

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47

Wagner, Paweł, and Maciej Kubicki. "3-Methyl-5-nitrouracil." Acta Crystallographica Section E Structure Reports Online 62, no. 4 (2006): o1257—o1259. http://dx.doi.org/10.1107/s1600536806007033.

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The molecules of the title compound, C5H5N3O4, are approximately planar. The nitro group makes a dihedral angle of 1.3 (4)° with the plane of the six-membered ring. This coplanar disposition is a reason for the changes in valence angles in the vicinity of the nitro group. Molecules are connected into dimers by means of N—H...O hydrogen bonds, and these dimers make larger structures with the help of relatively short C—H...O hydrogen bonds.

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48

Rißling, Julia-Katharina, Franz Petermann, and Jessica Melzer. "Der SET 3–5." Frühe Bildung 6, no. 1 (2017): 45–46. http://dx.doi.org/10.1026/2191-9186/a000301.

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49

Ali, Hapipah M., Subramaniam Puvaneswary, Wan Jefri Basirun, and Seik Weng Ng. "5-Methoxysalicylaldehyde 3-methoxybenzoylhydrazone." Acta Crystallographica Section E Structure Reports Online 61, no. 4 (2005): o947—o948. http://dx.doi.org/10.1107/s1600536805007154.

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50

Gainsford, Graeme J., and Keith Clinch. "3-Benzoyl-5-chlorouracil." Acta Crystallographica Section E Structure Reports Online 65, no. 2 (2009): o342. http://dx.doi.org/10.1107/s1600536809001287.

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