Academic literature on the topic 'Daniel 10-12'
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Journal articles on the topic "Daniel 10-12"
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Helmer, Matthias. "Daniel 10–12 als Schlüssel zum Buch." Biblische Zeitschrift 59, no. 1 (2015): 117–20. http://dx.doi.org/10.1163/25890468-059-01-90000009.
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Hill, Sarah. "Identities in Action Conference, Gregynog, 10–12 December 1999." Popular Music 19, no. 3 (2000): 394–95. http://dx.doi.org/10.1017/s0261143000000246.
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Daniel Chandler and Meic Llewellyn of the Department of Education at the University of Wales, Aberystwyth, nearly achieved the impossible in their construction of the Identities in Action conference. By allowing for the free interweaving of several identity discourses over a tantalisingly brief weekend, they provided a practical forum for the sympathetic mutual understanding of the studies of cultural- and self-identities, marginalised communities, minority languages, and gender and queer studies. Each block of time was organised into four different ‘strands’ which then culminated in workshops
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Quispe Parra, Maribel, and Victor A. Arias Santana. "Alteración postural en sedestación y su asociación al dolor lumbar en el personal administrativo del hospital III Daniel Alcides Carrión – Essalud Tacna 2017." REVISTA VERITAS ET SCIENTIA - UPT 8, no. 1 (2019): 1117–22. http://dx.doi.org/10.47796/ves.v8i1.116.
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Estudio realizado para medir si la alteración postural está asociado al dolor lumbar en el personal administrativo de los Hospital III Daniel Alcides Carrión Essalud Calana - Tacna 2017. Investigación observacional, analítica, prospectiva y de corte transversal, a nivel relacional. Se trabajó con el total del personal administrativo del Hospital III Daniel Alcides Carrión Essalud Calana - Tacna 2017, que cumplieron con los criterios de inclusión y exclusión de quienes se recopiló los datos de la ficha postural de sedestación, validada debidamente y llenada por los participantes. Se halló que e
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Hultgren, Stephen. "“A Vision for the End of Days”: Deferral of Revelation in Daniel and at the End of Mark." Zeitschrift für die neutestamentliche Wissenschaft 109, no. 2 (2018): 153–84. http://dx.doi.org/10.1515/znw-2018-0010.
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Abstract An important clue to the meaning of Mark 16,8 has not received adequate attention. The verse is an intertextual allusion to Dan 10,7. Daniel 10–12 establishes a pattern of revelation, concealment, and future revelation, in which the resurrection of the dead is apocalyptically deferred – its truth not confirmable until it happens at the end of days. A similar pattern of concealment and revelation characterizes Mark’s gospel. At the end of the gospel, the resurrection of Jesus is announced (and so revealed) in story time, but further concealed in discourse time. In the act of narrating,
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Jones, Graham. "25th November: Reign of Christ: 2 Samuel 23.1–7 and Psalm 132.1–12, (13–18); Daniel 7.9–10, 13–14; Psalm 93; Revelation 1.4b–8; John 18.33–37." Expository Times 130, no. 1 (2018): 31–33. http://dx.doi.org/10.1177/0014524618777065c.
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Sejkora, Jiří, and Bohuslav Bureš. "Arsenáty mědi z dobývky na žíle Geschieber - sever (patro Daniel), Svornost, jáchymovský rudní revír (Česká republika)." Bulletin Mineralogie Petrologie 28, no. 2 (2020): 454–65. http://dx.doi.org/10.46861/bmp.28.454.
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An interesting mineral association of Cu arsenates was found at abandoned ore stope at the Geschieber vein - north at the Daniel level of the Svornost mine, the Jáchymov ore district, Krušné hory, Czech Republic. Tangdanite forms thin tabular crystals up to 3 mm in size and coatings and fine crystalline aggregates on the area up to some cm2. It has light green, bluish-green to emerald green color and perfect cleavage. It is monoclinic, space group C2/c, the unit-cell parameters refined from X-ray powder diffraction data are: a 54.335(12), b 5.579(2), c 10.459(2) Å, β 95.42(3)° and V 3156(2) Å3
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Residente, Residente. "Infectología." Acta Médica Colombiana 43, no. 2S (2019): 117–75. http://dx.doi.org/10.36104/amc.2018.1399.
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 I-1 RESPUESTA PARADOJICA AL TRATAMIENTO ANTITUBERCULOSO EN UN PACIENTE CON TUBERCULOSIS MENINGEA Y ESPINAL, A PROPOSITO DE UN CASO (RESTREPO ANDREA, CLAVIJO ABSALÓN, GÓMEZ DIANA, AGUDELO CARLOS ANDRÉS)
 I-2 TRATAMIENTO EXITOSO CON FOSCARNET EN LESIONES ATÍPICAS DE VIRUS HERPES SIMPLE EN COINFECCIÓN CON VIRUS DE INMUNODEFICIENCIA HUMANA (RODRIGUEZ HERRERA DANIELA, PATIÑO GIRALDO SANTIAGO)
 I-3 LESIÓN RENAL AGUDA SECUNDARIO A TOXINA DE LONOMIA OBLIQUA (ARSANIOS DANIEL, QUINTERO ELIAS, SANTOYO NICOLÁS, MUÑOZ CARLOS)
 I-4 PIOMIOSITIS EN MUSLO POR PSEUDOMONAS (COGOLLO MARYSABE
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Moloney, Francis J. "The Book of Revelation: Hope in Dark Times." Religions 10, no. 4 (2019): 239. http://dx.doi.org/10.3390/rel10040239.
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Contemporary analysis of the world that produced the Book of Revelation suggests that Patmos was not a penal settlement, and there is little evidence that Domitian systematically persecuted Christians. The Emperor Cult was widely practiced, but Christians were not being persecuted for lack of participation. The document makes much of God’s victory in the death and resurrection of Jesus Christ, the slain and standing Lamb (Rev 5:6). The “saints” were not persecuted Asian Christians but, under the influence of the Book of Daniel, John’s presentation of those from Israel’s sacred history who live
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Kumar, Venkatachalam Sampath. "Grewia nagensium Prain vs Grewia denticulata Wall. ex Prain (Tiliaceae), which is to be accepted?" Phytotaxa 222, no. 1 (2015): 81. http://dx.doi.org/10.11646/phytotaxa.222.1.11.
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Prain (1900: 168) described the species Grewia nagensium based on specimens collected from Assam and Nagaland in Northeast India. Few months later, while preparing “A second century of new and rare Indian plants”, Prain (1901: 10) noted that his G. nagensium is indeed G. denticulata Wall. ex Voigt (1845: 128) and treated the former as a synonym of latter. However, “G. denticulata Wall. ex Voigt” is a nomen nudum as Voigt did not provide any description. Kanjilal et al. (1934) in their account of Flora of Assam mentioned only “Grewia denticulata, Wall. Ann. Roy. Bot. Gard. Calc. lx. 10. t. 12”
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Huapaya, Pedro, Yrma Espinoza, Alina Huiza, Carlos Sevilla, and Herman Vildosóla. "Tratamiento de Strongyloides stercoralis con ivermectina y tiabendazole." Anales de la Facultad de Medicina 64, no. 2 (2013): 89. http://dx.doi.org/10.15381/anales.v64i2.1433.
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OBJETIVO: Describir la experiencia del uso de ivermectina y tiabendazole en pacientes atendidos en el Instituto de Medicina Tropical “Daniel A. Carrión”- UNMSM. MATERIAL Y MÉTODOS: Durante los años 2001 y 2002, se administró ivermectina 0,2 mg/kg en dosis única a 22 pacientes (Grupo 1) o tiabendazole 25 mg/kg por 3 días a 20 pacientes (Grupo 2) con diagnóstico de Strongyloides stercoralis en heces. Se efectuó controles entre 20 y 40 días después de administrado el tratamiento. RESULTADOS: El promedio de edades fue 21,8 años (DE 22,6) para el grupo 1 y de 33,5 años (DE 14,2) para el grupo 2. Hu
Dissertations / Theses on the topic "Daniel 10-12"
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Linington, Silvia. "Covenant (berith) in Daniel and the Dead Sea Scrolls : an exposition of Daniel 9-12 and selected sections of the Damascus Document (CD), Community Rule (1QS), Hymns Scroll (1QHA) and War Scroll (1QM)." Thesis, 2014. http://hdl.handle.net/10500/18655.
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The following thesis comprises a systematic, synchronic study of the term בְּרִית (berîṯ,
covenant) in the book of Daniel, the Damascus Document, the Community Rule (Serekhha-
Yaḥad), the Hymn Scroll (Hodayot) and the War Scroll (Milḥamah). The basic text
used for Daniel is the BHS, and for the Dead Sea Scrolls the Dead Sea Scrolls Electronic
Library, supplemented by other editions.
Apart from an introduction (chapter 1), the work is divided into two sections. The
second chapter begins with a discussion of some introductory matters, such as the dating
and purpose of the book of Daniel.
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Tsai, Chung-Han, and 蔡忠翰. "An Analysis and Interpretation of Enrique Granados' Piano Pieces selected from Spanish Dances, Op. 37 with special focus on nos. 1, 5, 9, 10, 11 and 12." Thesis, 2008. http://ndltd.ncl.edu.tw/handle/90120463464388052498.
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碩士<br>輔仁大學<br>音樂研究所<br>97<br>The importance of Spanish piano music in western music history has always competed with the music that developed in German and Austrian regions. Although the exclusive style of Spanish folk music had been popular material for European music compositions from the 19th century, it was not until the Nationalists in music, that the “Golden Age of Spanish Piano Music” had finally arrived. In this alternation of the times, four leading Spanish composers, Isaac Albéniz, 1860-1909, Enrique Granados, 1867-1916, Manuel de Falla, 1876-1949, and Joaquín Turina, 1882-1949, show
Books on the topic "Daniel 10-12"
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Chotjewitz, David. Daniel half human and the good Nazi. Atheneum Books for Young Readers, 2004.
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Wildgruber, Regina. Daniel 10–12 als Schlüssel zum Buch. Mohr Siebeck, 2013. http://dx.doi.org/10.1628/978-3-16-152367-0.
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Strutture Denis Bigler Daniel Robert Hunziker Zeljka Marusic Andreas Helbling Mostra I Sotterranei Dellarte Antico Monastero Delle Agostiniane Monte Carasso 28 05 25 06 2006 Mirhajica Davide Cascio Martina Jacoma Ana Roldn Mostra I Sotterranei Dellarte Antico Monastero Delle Agostiniane Monte Carasso 15 10 12 11 2006. Capelli, 2007.
Find full textBook chapters on the topic "Daniel 10-12"
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"Chapter 4: Daniel 10–12." In Between Symbolism and Realism. Vandenhoeck & Ruprecht, 2011. http://dx.doi.org/10.13109/9783666550355.225.
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Taber, Douglass F. "Functionalization and Homologation of Alkenes." In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0029.
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Masahito Ochiai developed (Org. Highlights, March 24, 2008) the iodosobenzene-mediated cleavage of alkenes to keto aldehydes. Thottumkara K. Vinod of Western Illinois University described (Org. Lett. 2010, 12, 5640) a modified protocol that delivered the keto acid 2. Chi-Ming Che of the University of Hong Kong established (J. Am. Chem. Soc. 2010, 132, 13229) a method for the preparative scale Fe-catalyzed cis dihydroxylation of an alkene 3. Ilhyong Ryu of Osaka Prefecture University devised (Synlett 2010, 2014) a practical procedure for the free radical addition of HBr to an alkene 5. Tetsuo Ohta of Doshisha University showed (Tetrahedron Lett. 2010, 51, 2806) that a Ru catalyst could add an aromatic acid to the internal carbon of a terminal alkene 7. Noriki Kutsumura and Takao Saito of the Tokyo University of Science found (Org. Lett. 2010, 12, 3316) conditions for bromination/dehydrobromination to convert 10 to 11. Tsuyoshi Taniguchi of Kanazawa University oxidized (J. Org. Chem. 2010, 75, 8126) the alkene 12 to the nitro alkene 13. Professor Taniguchi added (Angew. Chem. Int. Ed. 2010, 49, 10154) methyl carbazate to 14 to give the β-hydroxy ester 15. Philippe Renaud of the University of Bern effected (J. Am. Chem. Soc. 2010, 132, 17511) the free radical homologation of 16 to the azide 18. Daniel P. Becker of Loyola University described (Tetrahedron Lett. 2010, 51, 3514) the elegant diastereoselective Pd-catalyzed bis-methoxycarbonylation of 19 to the diester 20. Matthew S. Sigman of the University of Utah established (J. Am. Chem. Soc. 2010, 132, 13981) the oxidative Heck arylation of 21 to 23. F. Dean Toste of the University of California, Berkeley, found (Org. Lett. 2010, 12, 4728) that the intermediate in the gold-catalyzed alkoxylation of 24 could couple to an aryl silane 25 to give 26. Chun-Yu Ho of the Chinese University of Hong Kong used (Angew. Chem. Int. Ed. 2010, 49, 9182) a Ni catalyst to add styrene 27 to the alkene 24. Masahiro Miura of Osaka University effected (J. Org. Chem. 2010, 75, 5421) the oxidative coupling of 29 with styrene 27 to give the linear product 30.
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Taber, Douglass F. "Construction of Oxygenated and Aminated Stereogenic Centers." In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0037.
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Computational analysis of the Novozyme 435 active site led (Tetrahedron Lett. 2010, 51, 309) Liyan Dai and Hongwei Yu of Zhejiang University, Hangzhou, to t-butanol for the enantioselective monoesterification of 1 to 2. Bruce H. Lipshutz of the University of California, Santa Barbara, devised (J. Am. Chem. Soc. 2010, 132, 7852) a Cu catalyst that mediated the enantioselective 1,2-reduction of α-branched enones such as 3. Qi-Lin Zhou of Nankai University found (J. Am. Chem. Soc. 2010, 132, 1172) that an α-alkoxy unsaturated acid 5 could be hydrogenated with high ee. Tohru Yamada of Keio University desymmetrized (J. Am. Chem. Soc. 2010, 132, 4072) the tertiary alcohol 7, delivering the enol lactone 8. Zachary D. Aron of Indiana University established (Organic Lett. 2010, 12, 1916) that the simple aldehyde 10 effected rapid racemization of the α-amino ester 9. Running the epimerization in the presence of an enantioselective esterase produced 11 high ee. Robert A. Batey of the University of Toronto devised (Organic Lett. 2010, 12, 260) a Pd catalyst for the enantioselective rearrangement of 12 to 13. In the course of a synthesis of dapoxetine, Hyeon-Kyu Lee of the Korea Research Institute of Chemical Technology showed (J. Org. Chem. 2010, 75, 237) that the Rh*-mediated intramolecular C-H insertion of 14 to 15, as developed by Du Bois, gave the opposite absolute configuration to that originally assigned. To prepare α-quaternary amines, Thomas G. Back of the University of Calgary explored (J. Org. Chem. 2010, 75, 1612) the selectivity of the PLE hydrolysis of esters such as 16. Daniel R. Fandrick and colleagues at Boehringer Ingelheim reported (J. Am. Chem. Soc. 2010, 132, 7600) a general method for the catalytic enantioselective propargylation of aldehydes, including 18. Dennis G. Hall of the University of Alberta devised (J. Am. Chem. Soc. 2010, 132, 5544) a route to α-hydroxy esters such as 22 by enantioselective conjugate addition to 21. Alexandre Alexakis of the University of Geneva prepared (Chem. Commun. 2010, 46, 4085) disubstituted epoxides such as 25 by the conjugate addition of 23 to 24.
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Taber, Douglass F. "Substituted Benzenes: The Saikawa/Nakata Synthesis of Kendomycin." In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0062.
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Jianbo Wang of Peking University described (Angew. Chem. Int. Ed. 2010, 49, 2028) the Au-promoted bromination of a benzene derivative such as 1 with N-bromosuccinimide. In a one-pot procedure, addition of a Cu catalyst followed by microwave heating delivered the aminated product 2. Jian-Ping Zou of Suzhou University and Wei Zhang of the University of Massachusetts, Boston, observed (Tetrahedron Lett. 2010, 51, 2639) that the phosphonylation of an arene 3 proceeded with substantial ortho selectivity. Yonghong Gu of the University of Science and Technology, Hefei, showed (Tetrahedron Lett. 2010, 51, 192) that an arylpropanoic acid 6 could be ortho hydroxylated with PIFA to give 7. Louis Fensterbank, Max Malacria, and Emmanuel Lacôte of UMPC Paris found (Angew. Chem. Int. Ed. 2010, 49, 2178) that a benzoic acid could be ortho aminated by way of the cyano amide 8. Daniel J. Weix of the University of Rochester developed (J. Am. Chem. Soc. 2010, 132, 920) a protocol for coupling an aryl iodide 10 with an alkyl iodide 11 to give 12. Professor Wang devised (Angew. Chem. Int. Ed. 2010, 49, 1139) a mechanistically intriguing alkyl carbonylation of an iodobenzene 10. This is presumably proceeding by way of the intermediate diazo alkane. Usually, benzonitriles are prepared by cyanation of the halo aromatic. Hideo Togo of Chiba University established (Synlett 2010, 1067) a protocol for the direct electrophilic cyanation of an electron-rich aromatic 15. Thomas E. Cole of San Diego State University observed (Tetrahedron Lett. 2010, 51, 3033) that an alkyl dimethyl borane, readily prepared by hydroboration of the alkene with BCl3 and Et3 SiH, reacted with benzoquinone 17 to give 18. Presumably this transformation could also be applied to substituted benzoquinones. When a highly substituted benzene derivative is needed, it is sometimes more economical to construct the aromatic ring. Joseph P. A. Harrity of the University of Sheffield and Gerhard Hilt of Philipps-Universität Marburg showed (J. Org. Chem. 2010, 75, 3893) that the Co-catalyzed Diels-Alder cyloaddition of alkynyl borinate 21 with a diene 20 proceeded with high regiocontrol, to give, after oxidation, the aryl borinate 22.
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Taber, Douglass F. "Organocatalysis of Carbocyclic Construction: The MacMillan Synthesis of (+)-Frondosin B." In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0071.
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One of the more powerful applications of organocatalysis has been the enantioselective transformation of preformed prochiral rings. In the five-membered ring series, Nobuyuki Mase of Shizuoka University effected (Synlett 2010, 2340) enantioselective addition of malonate to cyclopentenone 1, and Eric N. Jacobsen of Harvard University devised (Angew. Chem. Int. Ed. 2010, 49, 9753) a guanidinium catalyst for the Claisen rearrangement of 4 to 5. Jacek Mlynarski of Jagiellonian University accomplished (Tetrahedron Lett. 2010, 51, 4088) the enantioselective hydroxymethylation of 6. This worked equally well for cyclopentanone and cycloheptanone. The dynamic kinetic resolution/reductive amination of 8 described (Angew. Chem. Int. Ed. 2010, 49, 4612) by Benjamin List of the Max-Planck-Institut Mülheim worked best with cyclohexanones such as 8. Organocatalysts can also be effective for the construction of carbocyclic rings. Teck-Peng Loh of Nanyang Technological University found (Chem. Sci. 2010, 1, 739) a commercial phosphine catalyst that efficiently mediated the condensation of 10 with 11. David W. C. MacMillan of Princeton University used (J. Am. Chem. Soc. 2010, 132, 10015) a SOMO catalyst to combine 13 with 14 to make 15. Dawei Ma of the Shanghai Institute of Organic Chemistry employed (Org. Lett. 2010, 12, 3634) the Hayashi catalyst in the double Michael condensation of 16 with 17. Daniel Romo of Texas A&M University showed (Org. Lett. 2010, 12, 3764) that the appropriate organocatalyst could direct 19 to either diastereomer of the β-lactone 20. Professor Romo also reported (Angew. Chem. Int. Ed. 2010, 49, 9479) the desymmetrization of 2-alkyl cyclohexane-1,3-diones using a similar approach. In the six-membered ring series, José Alemán and José Luis García Ruano of the Universidad Autónoma de Madrid carried out (Eur. J. Org. Chem. 2010, 4482) Robinson annulation of 17 with 21. Ying-Chun Chen of Sichuan University, again using the Hayashi catalyst, reported (Angew. Chem. Int. Ed. 2010, 49, 6418) the addition of 17 to 23 to give 24. In another elegant application of visible light–mediated organocatalysis, Professor MacMillan described (Chem. Sci. 2010, 1, 37) the addition of the commercial boronic acid 25 to 17.
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"The Angler in the Environment: Social, Economic, Biological, and Ethical Dimensions." In The Angler in the Environment: Social, Economic, Biological, and Ethical Dimensions, edited by Jason Schratwieser, Stephen G. Sutton, and Robert Arlinghaus. American Fisheries Society, 2011. http://dx.doi.org/10.47886/9781934874240.ch1.
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<i>Abstract</i> .—The World Recreational Fishing Conference represents the only scientific meeting that is truly global, attracting scientists, managers, industry representatives, policy makers, and other stakeholders to discuss pertinent issues in recreational fisheries. The Fifth World Recreational Fishing Conference was held in Dania Beach, Florida, on November 10–12, 2008. This book represents the peer-reviewed proceedings of the landmark conference. Chapters in this book cover a range of issues such as governance, social and biological management tools and issues, ethics, and novel survey methods to advance the science and management of recreational fisheries.
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Taber, Douglass F. "Carbon–Carbon Bond Construction: The Baran Synthesis of (+)-Chromazonarol." In Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0026.
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Daniel J. Weix of the University of Rochester effected (Org. Lett. 2012, 14, 1476) the in situ reductive coupling of an alkyl halide 2 with an acid chloride 1 to deliver the ketone 3. André B. Charette of the Université de Montréal (not illustrated) developed (Nature Chem. 2012, 4, 228) an alternative route to ketones by the coupling of an organometallic with an in situ-activated secondary amide. Mahbub Alam and Christopher Wise of the Merck, Sharpe and Dohme UK chemical process group optimized (Org. Process Res. Dev. 2012, 16, 453) the opening of an epoxide 4 with a Grignard reagent 5. Ling Song of the Fujian Institute of Research on the Structure of Matter optimized (J. Org. Chem. 2012, 77, 4645) conditions for the 1,2-addition of a Grignard reagent (not illustrated) to a readily enolizable ketone. Wei-Wei Liao of Jilin University conceived (Org. Lett. 2012, 14, 2354) of an elegant assembly of highly functionalized quaternary centers, as illustrated by the conversion of 7 to 8. Antonio Rosales of the University of Granada and Ignacio Rodríguez-García of the University of Almería prepared (J. Org. Chem. 2012, 77, 4171) free radicals by reduction of an ozonide 9 in the presence of catalytic titanocene dichloride. In the absence of the acceptor 10, the dimer of the radical was obtained, presenting a simple alternative to the classic Kolbe coupling. Marc L. Snapper of Boston College found (Eur. J. Org. Chem. 2012, 2308) that the difficult ketone 12 could be methylenated following a modified Peterson protocol. Yoshito Kishi of Harvard University optimized (Org. Lett. 2012, 14, 86) the coupling of 15 with 16 to give 17. Masaharu Nakamura of Kyoto University devised (J. Org. Chem. 2012, 77, 1168) an iron catalyst for the coupling of 18 with 19. The specific preparation of trisubsituted alkenes is an ongoing challenge. Quanri Wang of Fudan University and Andreas Goeke of Givaudan Shanghai fragmented (Angew. Chem. Int. Ed. 2012, 51, 5647) the ketone 21 by exposure to 22 to give the macrolide 23 with high stereocontrol.
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Taber, Douglass F. "Organocatalyzed C–C Ring Construction: The Carreira Synthesis of (+)-Crotogoudin." In Organic Synthesis. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190646165.003.0069.
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Kazuaki Kudo of the University of Tokyo developed (Org. Lett. 2013, 15, 4964) a peptide catalyst for the enantioselective construction of 3 by the addition of 2 to 1. Thorsten Bach of the Technische Universität München devised (Science 2013, 342, 840; J. Am. Chem. Soc. 2013, 135, 14948) a Lewis acid organocatalyst for the photocyclization of 4 to 5. Albert Moyano of the Universitat de Barcelona effected (Eur. J. Org. Chem. 2013, 3103) enantioselective conjugate addition of 7 to 6 to give the cyclopentane 8. Daniel Romo of Texas A&M optimized (Nature Chem. 2013, 5, 1049) the addition of 9 to 10 to give the β-lactone 11. Kamal Kumar and Herbert Waldmann of the Technische Universität Dortmund found (Angew. Chem. Int. Ed. 2013, 52, 9576) that the addition of 12 to 13 followed by Bayer–Villiger oxidation and deacylation delivered 14 in high ee. David W. Lupton of Monash University opened (Angew. Chem. Int. Ed. 2013, 52, 9149) the cyclopropane of 15 in situ, leading to an ester enolate that added to 16 to give 17. Jeffrey S. Johnson of the University of North Carolina used (Chem. Sci. 2013, 4, 2828) an organocatalyst to mediate the addition of the prochiral 18 to 19, leading to 20. M. Belén Cid of the Universidad Autónoma de Madrid added (J. Org. Chem. 2013, 78, 10737) the nitroalkane 22 to the unsaturated aldehyde 21, leading, after intramolecular Julia-Kocienski addition, to the cyclohexene 23. Additions that proceed in high ee with cyclopentenone and cyclohexenone are often not as selective with cycloheptenone 24. Wei Wang of the University of New Mexico and Wenhu Duan of the Shanghai Institute of Materia Medica observed (Tetrahedron Lett. 2013, 54, 3791) that addition of nitromethane and of nitroethane to 24 were both highly effective. Strategies have been developed for applying organocatalysis to the assembly of polycarbacyclic ring systems. Sanzhong Luo of the Beijing National Laboratory for Molecule Sciences uncovered (Synthesis 2013, 45, 1939) a simple amine that efficiently catalyzed the Robinson annulation of 26 with 27 to give 28.
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Taber, Douglass. "Enantioselective Synthesis of Lactones and Cyclic Ethers." In Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0045.
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Developments in organocatalysis have turned toward the enantioselective construction of lactones. Shi-Wei Luo and Liu-Zhu Gong of the University of Science and Technology of China have found (J. Org. Chem. 2007, 71, 9905) that catalyzed addition of acetone to an α-hydroxy acid 1 proceeded with high ee. Esterification of the addition product followed by reduction and acid work-up delivered the lactone 4 with high dr and ee. In a complementary approach, Jean-Marc Vincent and Yannick Landais of the University Bourdeaux-1 showed (Chem. Commun. 2007, 4782) that catalyzed condensation of an aldehyde with an α-hydroxy acid 5 delivered the tetronic acid 8 in high ee. It may be that 8 could also be reduced with useful selectivity. Cong-Gui Zhao of the University of Texas, San Antonio has devised conditions (Organic Lett. 2007, 9, 2745) for the condensation of the keto phosphonates such as 10 with aldehydes to give, after oxidation, the δ-lactone 12. Carbohydrates such as glucose 13 are inexpensive, molecularly-complex starting materials. Subhash Chandra Taneja of the Indian Institute of Integrative Medicine, Jammu Tawi, has found conditions (J. Org. Chem. 2007, 72, 8965) for the single-step I2 -catalyzed transformation of 13 to 14, in which each of the alcohols have been differentiated. In a complementary approach described (Tetrahedron Lett. 2007, 48, 6389) by Tushar Kanti Chakraborty of the Indian Institute of Chemical Technology, Hyderabad, Ti-mediated reduction of 15 was shown to be highly diastereoselective, setting the two new stereogenic centers (marked by*) in 16. Building on work by Mead, Daniel Romo of Texas A&M has shown (J. Org. Chem. 2007, 72, 9053) that reductive cyclization of 18 also proceeded with high diastereocontrol, to give 19. As illustrated by the conversion of 20 to 21 reported (Tetrahedron Lett. 2007, 48, 7351) by Zsuzsa Juhász and László Somsák of the University of Debrecen, six-membered ring cyclic ethers can also be formed from carbohydrate precursors. Richard E. Taylor of the University of Notre Dame has taken advantage (Angew. Chem. Int. Ed. 2007, 46, 6874) of the “chemical chameleon” nature of a sulfone, using it both the stablilize the anion for intramolecular alkylation, to form 23, and as a leaving group, leading to 24.
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Taber, Douglass. "New Methods for the Stereoselective Construction of N-Containing Rings." In Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0053.
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Several methods have been reported for the stereocontrolled preparation of pyrrolidine and piperidine derivatives. Alison J. Frontier of the University of Rochester has observed (Organic Lett. 2007, 9, 4939) that hydrogenation of acyl pyrroles such as 1 gave good control not just around the ring, but also on the sidechain. Chi-Ming Che of the University of Hong Kong has devised ( J. Am. Chem. Soc. 2007, 129, 5828) a catalyst that converted amides such as 3 into the cyclized product 4, also with high diastereocontrol. Jean Ollivier of the Université de Paris-Sud, following the Sato procedure, has applied (Tetrahedron Lett. 2007, 48, 8765) the Kulinkovich reaction to allylated amino acid esters such as 5 , to give, after Fe-mediated fragmentation, the enantiomerically-pure piperidone 7 . Richard C. Hartley of the University of Glasgow has reported (J. Org. Chem. 2007, 72, 10287) what are, remarkably, the first examples of the aza-Petasis-Ferrier reaction, converting an ester such as 9, by carbonyl methylenation followed by Mannich cyclization, into the piperidone 10. Procedures for catalytic enantioselective C-N ring construction have also been developed. Armando Córdova of Stockholm University has shown (Tetrahedron Lett . 2007, 48, 8695) that condensation of 11 with 12 led to 14, which on reduction and hydrolysis delivered the 3-aryl proline 15. In an even simpler case, Santos Fustero of the Universidad de Valencia found (Organic Lett. 2007, 9, 5283) that the aldehyde 16 could cyclize to 17 with high ee. In a different approach (J. Am. Chem. Soc. 2007, 129, 14811), William E. Greenberg and Chi-Huey Wong of Scripps/La Jolla harnessed the power of an enzyme to mediate the addition of 19 to 18, leading to the pyrrolidine 21 . Daniel P. Furkert of the University of Bath has applied (Organic Lett. 2007, 9, 3769) the powerful Itsuno-Corey reduction to the piperidone 22, leading, after SN2’ displacement, to the alkene 23. To construct larger rings, Barry M. Trost of Stanford University has employed (Angew. Chem. Int. Ed. 2007, 46, 6123) his powerful Pd catalyst to effect opening of the racemic aziridine 24, leading, after metathesis, to the amine 27.
Conference papers on the topic "Daniel 10-12"
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Gimunová, Marta, Tomáš Vodička, Kristián Jánsky, et al. "The effect of classical ballet, Slovakian folklore dance and sport dance on static postural control in female and male dancers." In 12th International Conference on Kinanthropology. Masaryk University Press, 2020. http://dx.doi.org/10.5817/cz.muni.p210-9631-2020-4.
Full textAbstract:
Purpose: Classical ballet, Slovakian folklore dance, and sport dance training differ in their way how to master the art of dance; however, postural control is essential for the correct exe-cution of complex movements used in all types of dance. The aim of this study was to analyse the differences in static postural control between classical ballet dancers, Slovakian folklore dancers and sport dancers and to analyse the effect of body mass, body height and toe grip strength on postural control. Methods: 68 dancers, between 17 to 28 years of age, participated in this study: 21 dancers from Slova