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Journal articles on the topic '8.03.03.00-5'

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Published: 4 June 2021
Last updated: 12 February 2022

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1

Billiotte-Thieblemont, Nathalie. "(5 5)." L'en-je lacanien 33, no. 2 (2019): 193. http://dx.doi.org/10.3917/enje.033.0193.

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2

Choudhry, Ajai. "The Diophantine Equation $ax^5+by^5+cz^5=au^5+bv^5+cw^5$." Rocky Mountain Journal of Mathematics 29, no. 2 (1999): 459–62. http://dx.doi.org/10.1216/rmjm/1181071645.

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3

Ten Hoeve, W., H. Wynberg, E. E. Havinga, and E. W. Meijer. "Substituted 2,2':5',2'':5'',2''':5''',2'''':5'''',2''''': 5''''',2'''''':5'''''',2''''''':5''''''',2'''''''':5'''''''',2''''''''':5''''''''',2''''''''''-undecithiophenes, the longest characterized oligothiophenes." Journal of the American Chemical Society 113, no. 15 (1991): 5887–89. http://dx.doi.org/10.1021/ja00015a067.

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4

Patel, Bhisma Kumar, and Fritz Eckstein. "5′-Deoxy-5′-thioribonucleoside-5′-triphosphates." Tetrahedron Letters 38, no. 6 (1997): 1021–24. http://dx.doi.org/10.1016/s0040-4039(97)00084-1.

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5

Hegde, Vishnumurthy R., Katherine L. Seley, Stewart W. Schneller, and Thomas J. J. Elder. "5‘-Amino-5‘-deoxy-5‘-noraristeromycin." Journal of Organic Chemistry 63, no. 20 (1998): 7092–94. http://dx.doi.org/10.1021/jo972078c.

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6

TEN HOEVE, W., H. WYNBERG, E. E. HAVINGA, and E. W. MEIJER. "ChemInform Abstract: Substituted 2,2′:5′,2′′:5′′,2′′′:5′′′,2′′′′:5′′′′,2′′′′′:5′′′′′,2′′′′′′ :5′′′′′′,2′′′′′′′:5′′′′′′′,2′′′′′′′′:5′′′′′′′′,2′′′′′′′′′: 5′′′′′′′′′, 2′′′′′′′′′′-Undecithiophenes: The Longest Characterized Oligothiophenes." ChemInform 22, no. 42 (2010): no. http://dx.doi.org/10.1002/chin.199142165.

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7

Roy, Atanu, and Stewart W. Schneller. "Enantiospecific synthesis of 5′,5′,5′-trifluoro-5′-deoxyneplanocin A." Tetrahedron Letters 46, no. 51 (2005): 8913–15. http://dx.doi.org/10.1016/j.tetlet.2005.10.064.

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8

Das, Subha R., and Stewart W. Schneller. "The 5′-Nor Aristeromycin Analogues of 5′-Deoxy-5′-Methylthioadenosine and 5′-Deoxy-5′-Thiophenyladenosine." Nucleosides, Nucleotides and Nucleic Acids 33, no. 10 (2014): 668–77. http://dx.doi.org/10.1080/15257770.2014.917671.

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9

Turnbull, Douglas, Paul Hazendonk, Stacey D. Wetmore, and Michael Gerken. "Stabilisation of [WF 5 ] + and WF 5 by Pyridine: Facile Access to [WF 5 (NC 5 H 5 ) 3 ] + and WF 5 (NC 5 H 5 ) 2." Chemistry – A European Journal 26, no. 30 (2020): 6879–86. http://dx.doi.org/10.1002/chem.202000424.

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10

TAKATSU, Kiyoshi. "Interleukin-5, IL-5." Journal of Japan Atherosclerosis Society 23, no. 10 (1996): 599–603. http://dx.doi.org/10.5551/jat1973.23.10_599.

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11

Harrisville, Roy A. "Romans 5:1–5." Interpretation: A Journal of Bible and Theology 45, no. 2 (1991): 181–85. http://dx.doi.org/10.1177/002096430004500208.

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12

Guloksuz, Sinan, and Jim van Os. "Renaming schizophrenia: 5 × 5." Epidemiology and Psychiatric Sciences 28, no. 03 (2018): 254–57. http://dx.doi.org/10.1017/s2045796018000586.

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AbstractThere had been a long way to go before we felt comfortable about even discussing the issues revolving around the concept of ‘schizophrenia’, let alone reckoning on mere semantic revision. In this editorial, we aim to extend our discussion on the reasons behind the slow death of the concept of ‘schizophrenia’ and the benefits of changing the name and embracing a spectrum approach with an umbrella psychosis spectrum disorder (PSD) category (similar to autism spectrum disorder) that goes further than a mere semantic revision. We attempted to cover the topic of the renaming by providing fi
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13

Touzet, Patrick. "5/5 Michel Foucault." Soins Psychiatrie 36, no. 301 (2015): 45–46. http://dx.doi.org/10.1016/j.spsy.2015.09.008.

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14

Alyea, E. C., G. Ferguson, J. Malito, and B. L. Ruhl. "5-Phenyldibenzophosphole 5-selenide." Acta Crystallographica Section C Crystal Structure Communications 42, no. 7 (1986): 882–84. http://dx.doi.org/10.1107/s0108270186094192.

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15

Li, Weikuan, Xueqiang Yin, and Stewart W. Schneller. "5′-Fluoro-5′-deoxyaristeromycin." Bioorganic & Medicinal Chemistry Letters 18, no. 1 (2008): 220–22. http://dx.doi.org/10.1016/j.bmcl.2007.10.095.

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16

G. Micetich, Ronald, Chia C. Shaw, Tse W. Hall, et al. "The 5-Alkoxymethyl-, 5-Alkylthiomethyl-, and 5-Dialkylaminomethylisoxazoles." HETEROCYCLES 23, no. 3 (1985): 571. http://dx.doi.org/10.3987/r-1985-03-0571.

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17

HEGDE, V. R., K. L. SELEY, S. W. SCHNELLER, and T. J. J. ELDER. "ChemInform Abstract: 5′-Amino-5′-deoxy-5′-noraristeromycin." ChemInform 30, no. 7 (2010): no. http://dx.doi.org/10.1002/chin.199907253.

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18

Mori, Akira, Ryoji Mori, Manabu Takemoto, et al. "Troponoid metallomesogens with 5-alkoxy, 5-alkoxycarbonyl, 5-alkanoyloxy, 5-alkyl, 5-alkoxy-2-amino, and 5-alkoxy-2-alkylamino substituents." Journal of Materials Chemistry 15, no. 29 (2005): 3005. http://dx.doi.org/10.1039/b501974e.

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19

Sufrin, Janice R., Arthur J. Spiess, Debora L. Kramer, et al. "Targeting 5'-deoxy-5'-(methylthio)adenosine phosphorylase by 5'-haloalkyl analogs of 5'-deoxy-5'-(methylthio)adenosine." Journal of Medicinal Chemistry 34, no. 8 (1991): 2600–2606. http://dx.doi.org/10.1021/jm00112a039.

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20

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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21

Kennedy, Anne. "Researching children researching the world: 5×5×5=creativity." Early Years 30, no. 1 (2010): 95–96. http://dx.doi.org/10.1080/09575140903358133.

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22

Zhang, Cong, Christian Ludin, Marcel K. Eberle, Helen Stoeckli-Evans, and Reinhart Keese. "Asymmetric Synthesis of (S)-5,5,5,5?,5?,5?,5?-Hexafluoroleucine." Helvetica Chimica Acta 81, no. 1 (1998): 174–81. http://dx.doi.org/10.1002/hlca.19980810116.

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23

Chang, Shengmei, and Nan Zhu. "5:20:20:5 EFFICIENCY." PUPIL: International Journal of Teaching, Education and Learning 2, no. 2 (2018): 12–19. http://dx.doi.org/10.20319/pijtel.2018.22.1219.

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24

Eichberger, G�nter, Walter Hayden, Wolfgang Schwarz, and Herfried Griengl. "5-Ethylthiomethyl- und 5-Ethylsulfonylmethylpyrimidine." Monatshefte f�r Chemie Chemical Monthly 117, no. 3 (1986): 385–92. http://dx.doi.org/10.1007/bf00816533.

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25

Berman, Abraham, and Changqing Xu. "5×5 Completely positive matrices." Linear Algebra and its Applications 393 (December 2004): 55–71. http://dx.doi.org/10.1016/j.laa.2004.08.004.

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26

Walker, James K. "5-2-5 matrix system." Journal of the Acoustical Society of America 105, no. 2 (1999): 582. http://dx.doi.org/10.1121/1.426980.

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27

Schaible, H. G., J. W. Bats, and J. W. Engels. "5'-Azido-2',5'-dideoxythymidine." Acta Crystallographica Section C Crystal Structure Communications 51, no. 11 (1995): 2410–12. http://dx.doi.org/10.1107/s0108270195009310.

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28

Rivallan, Armel. "5/5 Ernest-Charles Lasègue." Soins Psychiatrie 38, no. 313 (2017): 45–46. http://dx.doi.org/10.1016/j.spsy.2017.09.010.

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29

Eknoian, M. W., T. R. Webb, S. D. Worley, A. Braswell, and J. Hadley. "5-(4-Pyridyl)-5-phenylhydantoin." Acta Crystallographica Section C Crystal Structure Communications 55, no. 3 (1999): 405–7. http://dx.doi.org/10.1107/s0108270198014528.

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30

Staff, EID Editorial. "Erratum Vol. 5, No. 5." Emerging Infectious Diseases 6, no. 3 (2000): 317. http://dx.doi.org/10.3201/eid0603.000318.

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31

Hegde, Vishnumurthy R., Katherine L. Seley, and Stewart W. Schneller. "Carbocyclic 5′-norcytidine (5′-norcarbodine)." Journal of Heterocyclic Chemistry 37, no. 5 (2000): 1361–62. http://dx.doi.org/10.1002/jhet.5570370558.

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32

Greif, Dieter. "5. Fachtagung Iminiumsalze (ImSaT 5)." Nachrichten aus der Chemie 50, no. 3 (2002): 387. http://dx.doi.org/10.1002/nadc.20020500328.

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33

Kubo, Kanji, Emi Yamamoto, and Akira Mori. "5-Cyanotropolone and 5-nitrotropolone." Acta Crystallographica Section C Crystal Structure Communications 57, no. 5 (2001): 611–13. http://dx.doi.org/10.1107/s0108270101002463.

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34

Villeneuve, Michael, and Don Wildfong. "Canada’s Top 5 in 5." Healthcare Quarterly 16, no. 3 (2013): 14–16. http://dx.doi.org/10.12927/hcq.2013.23505.

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35

Podgurskii, A. I., S. G. Zlotin, and O. A. Luk'yanov. "5-?-Nitroalkyl- and 5-?,?-dinitroalkyltetrazoles." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 35, no. 1 (1986): 215–16. http://dx.doi.org/10.1007/bf00952883.

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36

García Moro, María, Matías Astroza Rodríguez, Enrique García Merino, Enrique García Sánchez, and Jose Elías García Sánchez. "5 películas para 5 pandemias." Revista de Medicina y Cine 16, e (2021): 511–20. http://dx.doi.org/10.14201/rmc202016e511520.

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A lo largo de la historia diferentes pandemias han asolado a la humanidad. De todas ellas, salvo de la Covid-19, pues aún no ha habido tiempo de llevarla a la gran pantalla, ha habido numerosas representaciones en el cine comercial, algunas muy relevantes desde el punto de vista de la calidad cinematográfica y de la calidad científica con la que están documentados los guiones. Sería inalcanzable enumerar todas y cada una de ellas. Por tanto, en este artículo se plantea ofrecer a los lectores un ejemplo de cada una de estas pandemias (Peste, Viruela, Cólera, Gripe y VIH) que pueden ser útiles p
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37

Mascia, Laura, and Piero Luigi Ipata. "Activation pathways of 5-fluorouracil in rat organs and in PC12 cells11Abbreviations: PRPP, 5-phosphoribosyl 1-pyrophosphate; 5-FU, 5-fluorouracil; FUrd, 5-fluorouridine; 5-FUMP, 5-FUDP, and 5-FUTP, 5-fluorouridine 5′-mono-, -di-, and -triphosphate, 5-Fdeoxyuridine, 5-fluoro-2′-deoxyuridine; 5-FdeoxyUMP, 5-FdeoxyUDP, and 5-FdeoxyUTP, 5-fluoro-2′-deoxyuridine 5′-mono-, -di-, and triphosphate; Rib1-P, ribose 1-phosphate; and deoxyRib1-P, 2′-deoxyribose 1-phosphate." Biochemical Pharmacology 62, no. 2 (2001): 213–18. http://dx.doi.org/10.1016/s0006-2952(01)00650-5.

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38

Roth, B. "5-Hydroxytryptamine2-Family Receptors (5-Hydroxytryptamine2A, 5-Hydroxytryptamine2B, 5-Hydroxytryptamine2C) Where Structure Meets Function." Pharmacology & Therapeutics 79, no. 3 (1998): 231–57. http://dx.doi.org/10.1016/s0163-7258(98)00019-9.

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39

Crooks, Peter A., Trevor Deeks, and Francesco Desimone. "Synthesis of 5-benzoyl-5-phenyl- and 5-phenylhydroxymethyl-5-phenylhydantoins as potential anticonvulsants." Journal of Heterocyclic Chemistry 26, no. 4 (1989): 1113–17. http://dx.doi.org/10.1002/jhet.5570260439.

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40

Schlüter, H., I. Grobeta, J. Bachmann, et al. "Adenosine(5') oligophospho-(5') guanosines and guanosine(5') oligophospho-(5') guanosines in human platelets." Journal of Clinical Investigation 101, no. 3 (1998): 682–88. http://dx.doi.org/10.1172/jci119882.

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41

Kvasyuk, Evgeny I., Igor A. Mikhailopulo, Robert J. Suhadolnik, et al. "Synthesis and Biological Activity of 2′,5′-Oligoadenylate Trimers Containing 5′-Terminal 5′-Amino-5′-deoxy- and 5′-Amino-3′,5′-dideoxyadenosine Derivatives." Nucleosides and Nucleotides 18, no. 6-7 (1999): 1483–84. http://dx.doi.org/10.1080/07328319908044760.

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42

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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43

Creuven, Isabelle, Bernadette Norberg, Anne Olivier, et al. "5-(thien-2-yl) uracil analogs: 5-(5-methylthien-2-yl)-2′-deoxyuridine, 5-(5-thien-2-yl)-2′-deoxyuridine, and 5-(5-bromothien-2-yl)-2′-deoxyuridine." Journal of Chemical Crystallography 26, no. 11 (1996): 777–89. http://dx.doi.org/10.1007/bf01664656.

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44

Font, J., A. Gracia, and P. de March. "Synthesis of 5-alkyl-4-bromo-5-hydroxy-2(5)-furanones and 5-alkylidene-4-bromo-2(5)-furanones." Tetrahedron Letters 31, no. 38 (1990): 5517–20. http://dx.doi.org/10.1016/s0040-4039(00)97887-0.

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45

SUFRIN, J. R., A. J. SPIESS, D. L. KRAMER, et al. "ChemInform Abstract: Targeting 5′-Epoxy-5′-(methylthio)adenosine Phosphorylase by 5′-Haloalkyl Analogues of 5′-Deoxy-5′-(methylthio)adenosine." ChemInform 23, no. 2 (2010): no. http://dx.doi.org/10.1002/chin.199202319.

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46

G. Micetich, Ronald, Chia C. Shaw. Tse W. Hall, Paul Spevak, and Buljit K. Bains. "Lithiation Reactions of 5-Alkoxymethyl-, 5-Alkylthiomethyl-, and 5-Dialkylaminomethylisoxazoles." HETEROCYCLES 23, no. 3 (1985): 585. http://dx.doi.org/10.3987/r-1985-03-0585.

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47

Yang, Minmin, and Stewart W. Schneller. "Amino substituted derivatives of 5′-amino-5′-deoxy-5′-noraristeromycin." Bioorganic & Medicinal Chemistry 13, no. 3 (2005): 877–82. http://dx.doi.org/10.1016/j.bmc.2004.10.031.

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48

Sviridova, L. A., S. V. Afanas'eva, K. N. Zelenin, G. A. Golubeva, I. P. Bezhan, and Yu G. Bundel'. "Conversion of 5-hydroxy to 5-amino and 5-alkoxypyrazolidines." Chemistry of Heterocyclic Compounds 23, no. 4 (1987): 403–6. http://dx.doi.org/10.1007/bf00546735.

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49

Urjasz, Wojciech, Lech Celewicz, and Krzysztof Golankiewicz. "SYNTHESIS OF 5-ALKYLAMINO- AND 5-DIALKYLAMINO-5-DEOXYTHYMIDINE AND 5′-DEOXY-XYLO-THYMIDINE ANALOGS." Organic Preparations and Procedures International 27, no. 1 (1995): 109–13. http://dx.doi.org/10.1080/00304949509458188.

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50

Zhang, Biliang, Zhiyong Cui, and Lele Sun. "Synthesis of 5‘-Deoxy-5‘-thioguanosine- 5‘-monophosphorothioate and Its Incorporation into RNA 5‘-Termini." Organic Letters 3, no. 2 (2001): 275–78. http://dx.doi.org/10.1021/ol006916s.

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