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Journal articles on the topic 'Kohelet 5,9-6,6'

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Published: 4 June 2021
Last updated: 6 February 2022

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1

Heigerth, Günther. "Editorial 5–6/07." Österreichische Wasser- und Abfallwirtschaft 59, no. 5-6 (June 2007): A13. http://dx.doi.org/10.1007/s00506-007-0119-9.

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2

Graf, Thorsten, and Burkhard Koenig. "6-[5-(9H-Fluoren-9-ylmethoxycarbonylamino)-isophthalate]-amido-6-deoxy-b-cyclodextrine." Molbank 2003, no. 4 (June 28, 2003): M348. http://dx.doi.org/10.3390/m348.

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3

Fredericks, Daniel C. "Chiasm and Parallel Structure in Qoheleth 5:9-6:9." Journal of Biblical Literature 108, no. 1 (1989): 17. http://dx.doi.org/10.2307/3267468.

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4

Millichap, J. Gordon. "5-Hydroxytryptophan in Friedreich’s Ataxia." Pediatric Neurology Briefs 9, no. 6 (June 1, 1995): 44. http://dx.doi.org/10.15844/pedneurbriefs-9-6-6.

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5

Brömse, Michael. "Pfingstmontag – 5. 6. 2017 1. Mose 11,1–9." Homiletische Monatshefte 92, no. 7 (March 16, 2017): 395–99. http://dx.doi.org/10.13109/homh.2016.92.7.395.

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6

Novikova, L. N., B. A. Mazurchik, N. A. Ustynyuk, S. V. Kukharenko, and V. V. Strelets. "Inter-ring ?6??5 haptotropic rearrangements of 18? and 19? (?5-pentamethylcyclopentadienyl)(?6-9-methylfluorenyl)iron complexes." Russian Chemical Bulletin 43, no. 2 (February 1994): 299–303. http://dx.doi.org/10.1007/bf00695835.

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7

Witte, Markus. ""ABER GOTT WIRD MEINE SEELE ERLÖSEN" – TOD UND LEBEN NACH PSALM XLIX." Vetus Testamentum 50, no. 4 (2000): 540–60. http://dx.doi.org/10.1163/156853300506558.

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AbstractPs XLIX bildet, abzüglich der Überschrift und der Glossen in V 9 und V 15* (), eine literarisch einheitliche Meditation über das allgemeine Todesgeschick. Die des Sterbens aller Menschen kontrastiert der Psalmist mit der Hoffnung auf postmortale Auslösung seiner Seele () aus der Scheol. In V 15-6 deutet sich die von der Unsterblichkeit der Seele als eines von der äußeren Gestalt () Menschen zu unterscheidenden, dabei dessen Identität wahrenden Aspekts an. für die Theologie des Psalms ist die Verbindung von Glaube und Einsichtig zu sein () bedeutet, zwischen Leben und Tod bzw. Gottesmacht Menschenmacht differenzieren zu können und angesichts der Rätselhaftigkeit der auf den den Tod überwindenden Gott zu vertrauen. Literatur- und religionsgeschichtlich gehört der Psalm aufgrund seiner Parallelen zu Kohelet und zu Äthhen xcviii wohl in die zweite Hälfte des 3. Jh. v. Chr.
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8

McGlone, Lee. "Genesis 2:18–24; Ephesians 5:21–6:9." Review & Expositor 86, no. 2 (May 1989): 243–47. http://dx.doi.org/10.1177/003463738908600210.

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9

Stäblein, Christian. "Joh 1,1-5(6-8)9-15 26.12.2014 2. Weihnachtstag." Göttinger Predigtmeditationen 69, no. 1 (October 2014): 56–62. http://dx.doi.org/10.13109/gpre.2014.69.1.56.

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10

Schroeter-Wittke, Harald. "Lk 13,(1-5)6-9 18.11.2015 Buß- und Bettag." Göttinger Predigtmeditationen 69, no. 4 (June 2014): 507–12. http://dx.doi.org/10.13109/gpre.2014.69.4.507.

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11

Stäblein, Christian. "Joh 1,1-5(6-8)9-15 26.12.2014 2.Weihnachtstag." Pastoraltheologie 103, no. 11 (October 2014): 56–62. http://dx.doi.org/10.13109/path.2014.103.11.56.

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12

Schroeter-Wittke, Harald. "Lk 13,(1-5)6-9 18.11.2015 Buß- und Bettag." Pastoraltheologie 104, no. 8 (June 2015): 507–12. http://dx.doi.org/10.13109/path.2015.104.8.507.

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13

Baral, P. R., N. Ahmed, J. Kumar, S. Nair, and R. Nath. "Synthesis and physical properties of spin-1 honeycomb lattice Pb 6 Ni 9 (TeO 6 ) 5." Journal of Alloys and Compounds 711 (July 2017): 568–72. http://dx.doi.org/10.1016/j.jallcom.2017.04.010.

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14

Krinková, Jana, Martin Doležal, Jiřı́ Hartl, Vladimı́r Buchta, and Milan Pour. "Synthesis and biological activity of 5-alkyl-6-(alkylsulfanyl)- or 5-alkyl-6-(arylsulfanyl)pyrazine-2-carboxamides and corresponding thioamides." Il Farmaco 57, no. 1 (January 2002): 71–78. http://dx.doi.org/10.1016/s0014-827x(01)01156-9.

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15

Wrackmeyer, Bernd, and Alexandra Glöckle. "Synthesis of Pentaalkyl-6-bromo-2,3,4,5-tetracarba-nido-hexaboranes(6)." Zeitschrift für Naturforschung B 51, no. 6 (June 1, 1996): 859–64. http://dx.doi.org/10.1515/znb-1996-0616.

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Abstract Peralkylated 2,3,4,5-tetracarba-mdo-hexaboranes(6) 1 react with boron tribromide, BBr3, via selective exchange of the alkyl substituent in 6-position to give the corresponding new 6- bromo derivatives 2 in quantitative yield. The 6-iodo derivatives 2(1) can be prepared in the same way using BI3. Treatment of the carbaboranes 2 with Li Et3BH leads to the 1,2,3,4,5- pentaalkyl-2,3,4,5-tetracarba-inido-hexaboranes(6) 3. 1,3,4,6-Tetraethyl-2,3,4,5-tetracarbaw do-hexaborane(6) 4 reacts with BBr3 via degradation of the carbaborane cage to give EtBBr2, and (Z)-1,4-bis [bis(dibromoboryl)]-3-hexene 5. A new bis(diethylboryl)-substituted dialkenyl(bromo)borane 8 was prepared, but attem pts failed to convert it into a 1-bromo- or 6-bromo-mdo-C4B2-carbaborane. Treatment of 1,1-dialkyl-3-diethylboryl-4-ethylstannoles 9 with a large excess of BBr3 also affords 5, whereas 6-bromo-l,3,4-triethyl-2,3,4.5-tetracarbamdo- hexaborane(6) 11 was isolated in low yield (<5%) from the reaction between 9 and BBr3 (slight excess)
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16

Grygon, Christine A., William C. Fultz, Arnold L. Rheingold, and John L. Burmeister. "In search of geminites: The synthesis and structural characterization of [Pd{(C 6 H 5 ) 2 P(CH 2 ) n P(C 6 H 5 ) 2 }(SeCN) 2 ] ( n = 1,2,3)and [Pd{(C 6 H 5 ) 2 PCH 2 o C 6 H 4 CH 2 P(C 6 H 5 ) 2 }(SeCN) 2 ]." Inorganica Chimica Acta 144, no. 1 (April 1988): 31–35. http://dx.doi.org/10.1016/s0020-1693(00)80963-9.

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17

Kim, Seyeon, and Joon Hee Hong. "Synthesis and Biological Evaluation of 9-Deazaadenine 5′-Deoxy-6′,6′-Difluoro-CarbocyclicC-Nucleoside Phosphonic Acid Derivatives." Nucleosides, Nucleotides and Nucleic Acids 34, no. 10 (October 3, 2015): 708–28. http://dx.doi.org/10.1080/15257770.2015.1071847.

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18

Gitt, Michael A., Elizabeth T. Jordan, and Hakon Leffler. "Galectin-2, Galectins-5 and -9, and Galectins-4 and -6." Trends in Glycoscience and Glycotechnology 9, no. 45 (1997): 87–93. http://dx.doi.org/10.4052/tigg.9.87.

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19

Noetzel, Jutta. "Ex 12,1–4(5)6–8(9)10–14 9.4.2020 Gründonnerstag." Göttinger Predigtmeditationen 74, no. 2 (January 10, 2020): 228–34. http://dx.doi.org/10.13109/gpre.2019.74.2.228.

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20

Noetzel, Jutta. "Ex 12,1–4(5)6–8(9)10–14 9.4.2020 Gründonnerstag." Pastoraltheologie 109, no. 2 (January 10, 2020): 228–34. http://dx.doi.org/10.13109/path.2020.109.2.228.

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21

Baier, Ariane. "1. Sonntag nach Trinitatis - 22. 6. 2014 5 Mose 6,4 -9." Homiletische Monatshefte 89, no. 8 (April 2013): 357–60. http://dx.doi.org/10.13109/homh.2013.89.8.357.

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22

Maba, DL. "Diversity of Lactifluus (Basidiomycota, Russulales) in West Africa: 5 new species described and some considerations regarding their distribution and ecology." Mycosphere 6, no. 6 (2015): 737–59. http://dx.doi.org/10.5943/mycosphere/6/6/9.

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23

Hanna, Naeem B., Milena Masojídková, Pavel Fiedler, and Alois Pískala. "Synthesis of Some 6-Substituted 5-Azacytidines." Collection of Czechoslovak Chemical Communications 63, no. 2 (1998): 222–30. http://dx.doi.org/10.1135/cccc19980222.

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Protected 6-substituted benzyl, phenyl and chloromethyl derivatives of 5-azacytidine 8-10 have been prepared by addition of phenylacetyl- (2), benzoyl- (3) or (chloroacetyl)guanidine (4) to 2,3,5-tri-O-benzoyl-β-D-ribosyl isocyanate (1) and subsequent silylation-mediated cyclization of the obtained acyl(carbamoyl)guanidines 5-7. 4-Amino-6-phenyl-1,3,5-triazin-2(1H)-one (12) was obtained by condensation of carbamoylguanidine (13) with methyl benzoate in presence of methanolic sodium methoxide or by condensation of 13 with triethyl orthobenzoate in N,N-dimethylformamide. Stannic chloride catalyzed condensation of silylated 6-phenyl derivative 11 with 1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribose (14) in 1,2-dichloroethane afforded a 1.2 : 1 mixture of N1 and N3 nucleosides 9 and 15, respectively. Methanolysis of the protected compounds 8-10 and 15 gave the respective free nucleosides 16-19. The latter compounds inhibited the growth of bacteria E. coli B to a much lower extent than the unsubstituted 5-azacytidine.
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24

Sultana, Tanvir, and Md Wahab Khan. "A facile synthesis of 5-Iodo-6-substituted Pyrimidines from Uracil-6-Carboxylic acid (Orotic acid)." Dhaka University Journal of Pharmaceutical Sciences 12, no. 2 (January 12, 2014): 97–102. http://dx.doi.org/10.3329/dujps.v12i2.17613.

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2,4-Dichloro-pyrimidine-6-carbonylchloride (2) was synthesized by refluxing orotic acid (1) with phosphorus oxychloride and phosphorus pentachloride. Compound (2) underwent a smooth Friedel-Craft's reaction with a number of substituted benzene to yield 2,4-Dichloro-6-aroylpyrimidines 6 and 7 which were converted to the corresponding dimethoxy pyrimidines (8, 9) on treatment with sodium methoxide in methanol. The iodination reaction on 2,4-dimethoxy-6-aroylpyrimidines (8, 9) was attempted by several methods but only NIS-TFA-TFAA method gave the desired products, 2,4-dimethoxy-5-iodo-6-aroylpyrimidine (10, 11) in good yields. Dhaka Univ. J. Pharm. Sci. 12(2): 97-102, 2013 (December) DOI: http://dx.doi.org/10.3329/dujps.v12i2.17613
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25

Huang, Bei, Petr Starostik, Hannelore Schraut, J�rgen Krauss, Niels S�rensen, and Wolfgang Roggendorf. "Human ependymomas reveal frequent deletions on chromosomes 6 and 9." Acta Neuropathologica 106, no. 4 (October 1, 2003): 357–62. http://dx.doi.org/10.1007/s00401-003-0739-5.

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26

Roque Bravo, Rita, Helena Carmo, João Pedro Silva, Maria João Valente, Félix Carvalho, Maria de Lourdes Bastos, and Diana Dias da Silva. "Emerging club drugs: 5-(2-aminopropyl)benzofuran (5-APB) is more toxic than its isomer 6-(2-aminopropyl)benzofuran (6-APB) in hepatocyte cellular models." Archives of Toxicology 94, no. 2 (December 14, 2019): 609–29. http://dx.doi.org/10.1007/s00204-019-02638-9.

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27

Wint, Lewin T., and Peter A. McCarthy. "Synthesis of tritium labelled (3R*, 5S*)-3, 5-dihydroxy-9, 9-diphenyl-6, 8-nonadienoate." Journal of Labelled Compounds and Radiopharmaceuticals 25, no. 11 (November 1988): 1289–97. http://dx.doi.org/10.1002/jlcr.2580251116.

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28

Chen, Yunfeng, Ting Gao, Wei Li, Ning Li, and Junyan Ren. "A dual-mode 6–9 GHz transmitter for OFDM-UWB." Journal of Semiconductors 32, no. 5 (May 2011): 055004. http://dx.doi.org/10.1088/1674-4926/32/5/055004.

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29

François DEZIER, Jean. "Livres: 2es «Journées scientifiques Alain Feuillu» 5-6 novembre 2015." Revue Francophone des Laboratoires 2015, no. 475 (September 2015): 25. http://dx.doi.org/10.1016/s1773-035x(15)30240-9.

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30

De Reuver, R. "Over grenzen (Deuteronomium 5:32-6:3 en Matteüs 12:9-15)." Theologia Reformata 62, no. 2 (June 1, 2019): 110–14. http://dx.doi.org/10.21827/5ccffa6a07723.

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31

Akiyama, Kengo. "Reproof in cd 9:2–8 and 1QS 5:24–6:1." Dead Sea Discoveries 24, no. 2 (September 8, 2017): 301–6. http://dx.doi.org/10.1163/15685179-12341430.

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Abstract The Damascus Document (cd 9:2–8) and the Serekh (1QS 5:24–6:1) amplify Leviticus 19:17–18 and carefully spell out the legal procedure for open reproof. In doing so, however, they both omit the key phrase of Leviticus 19:18b (ואהבת לרעך כמוך). This short note suggests that the omission is deliberate and results from a specific sectarian reading of Leviticus 19:17–18. The sectarians are construing this scriptural mandate as a legal command in contrast to the more mainstream reading as exhortation in the Second Temple period.
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32

Blaum, M. "A (16, 9, 6, 5, 4) error-correcting DC free block code." IEEE Transactions on Information Theory 34, no. 1 (January 1988): 138–41. http://dx.doi.org/10.1109/18.2613.

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33

Puttkammer, Detlef. "2. Weihnachtstag - 26. 12. 2014 Johannes 1,1-5(6-8)9 -14." Homiletische Monatshefte 90, no. 2 (October 2014): 57–60. http://dx.doi.org/10.13109/homh.2014.90.2.57.

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34

Ekberg, J. O., J. F. Seely, U. Feldman, and C. M. Brown. "3p^6 3d^8–3p^5 3d^9 Transitions in ironlike Sb." Journal of the Optical Society of America B 6, no. 9 (September 1, 1989): 1648. http://dx.doi.org/10.1364/josab.6.001648.

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35

Pufeng, Chen, Li Zhiqiang, Wang Xiaosong, Zhang Haiying, and Ye Tianchun. "A 6–9 GHz 5-band CMOS synthesizer for MB-OFDM UWB." Journal of Semiconductors 31, no. 7 (July 2010): 075001. http://dx.doi.org/10.1088/1674-4926/31/7/075001.

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36

Vlasenko, E., M. Schülein, J. Cherry, and F. Xu. "Substrate specificity of family 5, 6, 7, 9, 12, and 45 endoglucanases." Bioresource Technology 101, no. 7 (April 2010): 2405–11. http://dx.doi.org/10.1016/j.biortech.2009.11.057.

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37

Waring, P., and WLF Armarego. "Pterins. X. A New Preparation of 6-Hydroxymethylpterin from 6-Methylpterin." Australian Journal of Chemistry 38, no. 4 (1985): 629. http://dx.doi.org/10.1071/ch9850629.

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6-Hydroxymethylpterin was prepared in c. 80% overall yield via 2- acetamido-6-methylpteridin-4(3H)-one, oxidation with lead tetraacetate to 2-acetamido-6-acetoxymethylpteridin-4(3H)-one and hydrolysis. The 2-acetamido-6-methylpterin was prepared isomerically pure by acetylation of a mixture of 6- and 7-methylpterin prepared by condensation of 2,5,6-triaminopyrimidin-4(3H)-one with methylglyoxal at 0-5°. Under these conditions the ratio of 6-methyl- to 7-methylpterin is considerably improved (9 : 1).
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38

Ren, Huixue, Yanzhao Yang, Jimao Lin, Yinshan Qi, and Yeqing Zhang. "Synthesis and characterization of 5-bromo-3-sec-butyl-6-methyluracil." Frontiers of Chemistry in China 3, no. 2 (April 4, 2008): 152–56. http://dx.doi.org/10.1007/s11458-008-0029-9.

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39

Ivanov, S. M., L. M. Mironovich, and E. D. Daeva. "Synthesis and structure of 6-tert-butyl-5-triphenylgermyl-1,2,4-triazines." Russian Chemical Bulletin 70, no. 7 (July 2021): 1394–99. http://dx.doi.org/10.1007/s11172-021-3229-9.

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40

Ming-Lun, Chen, and Yu Xiao-Guang. "Spectra and oscillator strengths of 3p 6 3d 9 –3p 5 3d 10 and 3p 6 3d 9 –3p 6 3d 8 4p transitions for cobalt-like Sn 23 + ion." Chinese Physics B 18, no. 1 (January 2009): 157–60. http://dx.doi.org/10.1088/1674-1056/18/1/024.

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41

Yao, Juan, Weijian Ye, Jinliang Liu, Juanjuan Liu, and Cunde Wang. "Synthesis and cytotoxicity of (3β)-3-acetyloxy-5(6)-androsten-7-one oxime and 3,5(6)-androstadien-7-one oxime." Medicinal Chemistry Research 23, no. 4 (September 21, 2013): 1839–43. http://dx.doi.org/10.1007/s00044-013-0788-9.

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42

Bould, Jonathan, Paul Brint, John D. Kennedy, Mark Thornton-Pett, Lawrence Barton, and Nigam P. Rath. "Metallaborane Reaction Chemistry. Part 3. Reaction of Carbon Monoxide with [6-H-6-(PPh3)-6P,5C-μ-(2-Ph2PC6H4)-nido-6-IrB9H12] and the Isolation and Characterisation of Two arachno-6-Monoiridadecaboranes [6-(CO)-6-H-6,9-(PPh3)2-6P,5C-μ-(2-Ph2PC6H4)-arachno-6-IrB9H11] and sym-[6-(CO)-6-H-6,6-(PMe2Ph)2-9-(PPh3)-arachno-6-IrB9H11]." Collection of Czechoslovak Chemical Communications 62, no. 8 (1997): 1239–53. http://dx.doi.org/10.1135/cccc19971239.

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[6-(CO)-6-H-6,9-(PPh3)2-6P,5C-μ-(2-Ph2PC6H4)-arachno-6-IrB9H11] (1) results from the reaction of [6-H-6-(PPh3)-6P,5C-μ-(2-Ph2PC6H4)-nido-6-IrB9H12] (2) with carbon monoxide in refluxing benzene. It is characterised by NMR spectroscopy and by single-crystal X-ray diffraction analysis. Crystals were triclinic, space group P1, with a = 10.688(2), b = 13.114(3), c = 22.356(5) Å, α = 78.33(2), β = 89.482(10), γ = 70.884(12)°, and Z = 2. The compound is of the little-examined arachno ten-vertex metallaborane structural type. A second compound of this type, [6-(CO)-6-H-6,6-(PMe2Ph)2-9-(PPh3)-arachno-6-IrB9H11] (3), isolated from a reaction system involving [Ir(CO)Cl(PPh3)2], PMe2Ph and the [nido-B9H12]- anion, has also been characterised crystallographically. Crystals were triclinic, space group P1, with a = 10.389(1), b = 10.511(1), c = 19.699(3) Å, α = 75.03(1), β = 85.53(1), γ = 74.88(1)°, and Z = 2.
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43

Santosa, Santosa. "Urgensi Peran Orang Tua Membangun Kepemimpinan Anak di Era Disrupsi Teknologi Berdasarkan Ulangan 6: 6-9." EDULEAD: Journal of Christian Education and Leadership 2, no. 1 (June 1, 2021): 71–88. http://dx.doi.org/10.47530/edulead.v2i1.61.

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Technological disruption has an impact on fundamental changes in the order of human life. The disruption of technology has a positive and negative impact on human life. Facing the change and the impact of the technological disruption, the role of parents is very important in shaping leadership in children. This research was conducted by studying literature and text analysis of the Book of Deuteronomy 6:6-9. The results of this study aim to describe the urgency of the role of parents in building children's leadership according to Deuteronomy 6:6-9 in an era of technological disruption. The conclusion is the urgency of the role of parents in building children's leadership in an era of technological disruption according to Deuteronomy 6:6-9, among others: 1) To become spiritual educators of children. 2) Become a role model for spiritual discipline. 3) Discipline the spiritual growth of children. 4) Improve the relationship with children. 5) Give children responsibility for their spiritual growth. 6) Become a role model in healthy social media.AbstrakDisrupsi teknologi berdampak terhadap perubahan tatanan kehidupan manusia secara fundamental. Disrupsi teknologi memberi dampak positif dan negatif bagi kehidupan manusia. Menghadapi perubahan dan dampak akibat disrupsi teknologi, peran orang tua sangat penting dalam membentuk kepemimpinan dalam diri anak. Penelitian ini dilakukan dengan studi literatur dan analisis teks Kitab Ulangan 6: 6-9. Hasil penelitian ini bertujuan mendiskripsikan urgensi peran orang tua membangun kepemimpinan anak menurut Kitab Ulangan 6: 6-9 di era disrupsi teknologi. Diperoleh kesimpulan urgensi peran orang tua membangun kepemimpinan anak di era disrupsi teknologi menurut Ulangan 6: 6-9 antara lain: 1) Menjadi pendidik rohani Anak. 2) Menjadi role model disiplin rohani. 3) Mendisiplin pertumbuhan rohani anak. 4) Meningkatkan relasional dengan anak. 5) Memberi tanggungjawab anak terhadap pertumbuhan rohaninya. 6) Menjadi role model bermedia sosial sehat.
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44

Sun, Jin, Jia-jian Shen, Yan-ping Zhang, and Jin-jiang Sun. "Compact cores of molecular clouds in NGC 1333/IRAS 6–9." Chinese Astronomy and Astrophysics 24, no. 4 (October 2000): 511–21. http://dx.doi.org/10.1016/s0275-1062(00)00082-5.

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45

Broome, M., I. Dojcinovic, and M. Richter. "O 9-6 Fistules carotido-caverneuses : complications de traumatismes maxillo-faciaux." Revue de Stomatologie et de Chirurgie Maxillo-faciale 106, no. 4 (September 2005): 37. http://dx.doi.org/10.1016/s0035-1768(05)85945-5.

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46

Rohde, Ralph, Günter Neef, Gerhard Sauer, and Rudolf Wiechert. "Stereoselective epoxidation of 5(10),9(11)-estradienes." Tetrahedron Letters 26, no. 17 (1985): 2069–72. http://dx.doi.org/10.1016/s0040-4039(00)94781-6.

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47

Solladié, Guy, Nicolai Gehrold, and Jean Maignan. "Synthesis of (+)-(R)-5-hydroxy-6-hydroxymethyl-7-methoxy-8-methylflavanone." Tetrahedron: Asymmetry 10, no. 14 (July 1999): 2739–47. http://dx.doi.org/10.1016/s0957-4166(99)00266-9.

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48

Das, Palas, C. P. Spears, A. H. Shahinian, Swapan K. Dasgupta, and Nitya G. Kundu. "Palladium-catalysed synthesis of some biologically active 5, 6-disubstituted uracils." Bioorganic & Medicinal Chemistry Letters 6, no. 20 (October 1996): 2477–80. http://dx.doi.org/10.1016/0960-894x(96)00451-9.

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49

Uzbekov, Vyacheslav V., Samat A. Talipov, Bakhtiyar T. Ibragimov, Robert D. Stipanovic, and Jinggao Liu. "Desoxyhemigossypol 6-methyl ether." Acta Crystallographica Section E Structure Reports Online 69, no. 2 (January 31, 2013): o302. http://dx.doi.org/10.1107/s1600536813002304.

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Abstract:
The title sesquiterpene [systematic name: 6-methoxy-10-methyl-7-(propan-2-yl)-2-oxatricyclo[6.3.1.04,12]dodeca-1(11),4,6,8(12),9-pentaen-5-ol], C16H18O3, was isolated from pathogen-infected stele tissue ofGossypium barbadense. There are two molecules in the asymmetric unit and the dihedral angle between their naphthofuran systems is 86.48 (2)°. In the crystal, O—H...O hydrogen bonds between the hydroxy groups and etheric O atoms link the molecules into centrosymmetric tetramers. These tetramers are assembled into (010) layersviastacking interactions between the naphthofuran systems [interplanar distance 3.473 (3) Å] and short C—H...O contacts.
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50

Bischoff, 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.

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Abstract:
The Mannich reaction of 7-aryl-5,6-dihydropyrido[2,3-d]pyrimidines 3, easily accessible by condensation of 6-amino-1,3-dimethyluracil (1) with Mannich bases 2a - c, gives rise to a mixture of 7-aryl-6-(N,N-dimethylaminomethyl)pyrido[2,3-d]pyrimidines 6 and 7 as well as 1,2-bis- (7-arylpyrido[2,3-d]pyrimidin-6-yl)ethane 13 the ratio of which depends on the reaction conditions and the amine used. 6-Alkylamino-1,3-dimethyluracils 15 - 18 were converted to the corresponding 5-(3-oxo-3-phenylpropyl)uracils 19 - 22 by condensation with the Mannich base 2a. Ring closure of 19 - 22 was performed by Vilsmeier formylation to afford the 8-alkyl- and 7,8-diaryl-5,8- dihydropyrido[2,3-d]pyrimidine-6-carbaldehydes 9 - 12 via the corresponding iminium salts 27 - 30
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