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Journal articles on the topic 'Cadogan'

Author: Grafiati

Published: 4 June 2021

Last updated: 27 January 2023

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1

Carson, Hastings, and Jack Cadogan. "Florence Cadogan." BMJ 333, no. 7578 (2006): 1126.2–1126. http://dx.doi.org/10.1136/bmj.39034.670394.fa.

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2

Qu, Zhonghua, Pu Wang, Xing Chen, Guo-Jun Deng, and Huawen Huang. "Visible-light-driven Cadogan reaction." Chinese Chemical Letters 32, no. 8 (2021): 2582–86. http://dx.doi.org/10.1016/j.cclet.2021.02.047.

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3

Singh, Neetu, Ga Hee Noh, Hyoung-Ryun Park, and Junseong Lee. "Crystal structure, Hirshfeld surface and photophysical analysis of 2-nitro-3-phenyl-9H-carbazole." Acta Crystallographica Section E Crystallographic Communications 77, no. 9 (2021): 887–90. http://dx.doi.org/10.1107/s2056989021007726.

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The title compound, C18H12N2O2, was synthesized from a dinitrobiphenylbenzene derivative using a novel modification of the Cadogan reaction. The reaction has several possible ring-closed products and the title compound was separated as the major product. The X-ray crystallographic study revealed that the carbazole compound crystallizes in the monoclinic P\overline{1} space group and possesses a single closed Cadogan ring. There are two independent molecules in the asymmetric unit. In the crystal, the molecules are linked by N—H...O hydrogen bonding.

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4

Li, Jie Jack. "ChemInform Abstract: Cadogan-Sundberg Indole Synthesis." ChemInform 43, no. 20 (2012): no. http://dx.doi.org/10.1002/chin.201220242.

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5

Kaur, Manpreet, and Raj Kumar. "C‐N and N‐N bond formation via Reductive Cyclization: Progress in Cadogan /Cadogan‐Sundberg Reactionǂ." ChemistrySelect 3, no. 19 (2018): 5330–40. http://dx.doi.org/10.1002/slct.201800779.

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6

Shuvalov, Vladislav, Anna Rupp, Anna Kuratova, Alexander Fisyuk, Andrey Nefedov та Galina Sagitullina. "Synthesis of δ-Carbolines and the Alkaloid Quindoline through a Molybdenum-Catalyzed Cadogan Cyclization and their Photoluminescent Properties". Synlett 30, № 08 (2019): 919–23. http://dx.doi.org/10.1055/s-0037-1612416.

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Cadogan reductive cyclization of substituted 2-aryl-3-nitropyridines to give δ-carbolines was performed under MoO2Cl2(DMF)2 catalysis with triphenylphosphine as a ligand. A new approach for the synthesis of the alkaloid quindoline based on a Mo(VI)-catalyzed Cadogan reductive cyclization of 2-phenyl-3-nitro-5,6,7,8-tetrahydroquinoline followed by aromatization of the resulting 2,3,4,10-tetrahydro-1H-indolo[3,2-b]quinoline is proposed. Various о-nitroarylpyridines, obtained by reacting acylpyruvates and cyclic hydroxymethylene ketones with nitroacetophenone enamines, were used as starting compo

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7

Huang, Hongyan, Quan Li, Meng Qiu, et al. "D–A conjugated polymers based on thieno[3,2-b]indole (TI) and 2,1,3-benzodiathiazole (BT) derivatives: synthesis, characterization and side-chain influence on photovoltaic properties." RSC Advances 6, no. 51 (2016): 45873–83. http://dx.doi.org/10.1039/c6ra05413g.

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8

Srour, Hassan, Thu-Hong Doan, Elisabeth Da Silva, Richard J. Whitby, and Bernhard Witulski. "Synthesis and molecular properties of methoxy-substituted diindolo[3,2-b:2′,3′-h]carbazoles for organic electronics obtained by a consecutive twofold Suzuki and twofold Cadogan reaction." Journal of Materials Chemistry C 4, no. 26 (2016): 6270–79. http://dx.doi.org/10.1039/c6tc02009g.

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A set of methoxy-substituted diindolo[3,2-b:2′,3′-h]carbazoles has been synthesized by twofold Suzuki–Miyaura, Cadogan andN-alkylation reactions starting fromN-hexyl-2,7-dibromo-3,6-dinitro carbazole.

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9

Shaw, Tony. "Cadogan's last fling: Sir Alexander Cadogan, Chairman of the board of governors of the BBC." Contemporary British History 13, no. 2 (1999): 126–45. http://dx.doi.org/10.1080/13619469908581533.

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10

Castiñeira Reis, Marta, Marta Marín-Luna, Carlos Silva López, and Olalla Nieto Faza. "Mechanism of the Molybdenum-Mediated Cadogan Reaction." ACS Omega 3, no. 6 (2018): 7019–26. http://dx.doi.org/10.1021/acsomega.8b01278.

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11

Lapuente Garrido, Ivan. "Orientação para o mercado externo: o refinamento de uma escala de mensuração." Revista de Administração de Empresas 47, no. 4 (2007): 116–30. http://dx.doi.org/10.1590/s0034-75902007000400010.

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O presente estudo consiste em um survey exploratório de corte transversal único, realizado com 617 empresas exportadoras brasileiras, desenvolvido com o objetivo de validar, no Brasil, uma escala de orientação para o mercado externo. Utilizou-se a modelagem de equações estruturais como base para a análise estatística dos dados coletados. Duas escalas de mensuração de orientação para o mercado serviram de referência para o estudo - a escala de orientação para o mercado externo de Cadogan, Diamantopoulos e Mortanges (1999) e a escala de orientação para o mercado de Matsuno, Mentzer e Rentz (2000

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12

Hunting, Penelope. "William Cadogan (1711–97): colossus of child care." Journal of Medical Biography 19, no. 4 (2011): 182–83. http://dx.doi.org/10.1258/jmb.2011.011056.

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13

Goo, Deuk-Young, and Sang Kook Woo. "One-pot synthesis of carbazoles via tandem C–C cross-coupling and reductive amination." Organic & Biomolecular Chemistry 14, no. 1 (2016): 122–30. http://dx.doi.org/10.1039/c5ob01952d.

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We have developed a highly efficient synthetic route to carbazoles that employs sequential C–C/C–N bond formation via Suzuki cross-coupling and Cadogan cyclization. The developed method is compatible with electron neutral, rich or deficient substrates. The synthetic utility of this method was demonstrated by the concise syntheses of four natural products.

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14

Diegues, Douglas. "TRANS AYVU RAPYTA: selección, traducciones y gravuras de Douglas Diegues." Língua-lugar : Literatura, História, Estudos Culturais, no. 4 (April 6, 2022): 162–97. http://dx.doi.org/10.34913/journals/lingualugar.2021.e718.

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   Depois de mais de 30 años leyendo, releyendo, estudando el Ayvu Rapyta, los textos míticos de los Mbyá-Guaraní del Guairá, Paraguay, coligidos y traduzidos al castellano-paraguayo por León Cadogan, imaginei uma trans-inbención visual de la poesía contenida en estos cantos cosmogônicos, que pudesse ser apreciada por los adultos y también por las crianzas.  

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15

Keller, Q. Alejandro, Analía Pirondo, and Pablo Stampella. "El cultivo del ricino y el amba’y en comunidades guaraníes del Nordeste Argentino, aproximación etnobotánica de su historia y cosmología." Bonplandia 27, no. 1 (2018): 23. http://dx.doi.org/10.30972/bon.2712983.

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Se estudian evidencias históricas sobre el cultivo del “amba’y”, Cecropia pachystachya (Urticaceae) en ámbitos domésticos de comunidades guaraníes y su reemplazo por el “ricino”, Ricinus communis (Euphorbiaceae), cuyo cultivo constituye aún una práctica corriente. Información obtenida sobre los usos del ricino y sobre el origen mítico del amba’y aportan información útil para lograr una aproximación etimológica al fitónimo “amba’y” alternativa a las propuestas previamente por León Cadogan

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16

McDermott, John V. "Betjeman's the Arrest of Oscar Wilde at the Cadogan Hotel." Explicator 57, no. 3 (1999): 165–66. http://dx.doi.org/10.1080/00144949909596857.

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17

Majgier-Baranowska, Helena, John D. Williams, Bing Li, and Norton P. Peet. "Studies on the mechanism of the Cadogan–Sundberg indole synthesis." Tetrahedron Letters 53, no. 35 (2012): 4785–88. http://dx.doi.org/10.1016/j.tetlet.2012.06.146.

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18

Cunha Ramos Quaresma, Carline, and Izabela Guimarães Guerra Leal. "KAKÁ WERÁ JECUPÉ E A TRADUÇÃO DOS CANTOS SAGRADOS MBYÁ GUARANI." Letras Escreve 8, no. 1 (2018): 533. http://dx.doi.org/10.18468/letras.2018v8n1.p533-554.

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<p>No presente trabalho, focalizamos a tradução dos cantos sagrados Mbyá Guarani realizada por Kaká Werá Jecupé, que possui um valor peculiar advindo do fato de Kaká ser membro da cultura traduzida. Neste sentido, nossos objetivos são: discutir a especificidade da tradução de Kaká Werá Jecupé e traçar eixos comparativos entre a sua tradução e as de Léon Cadogan (1959), Pierrre Clastres (2011), e Josely Vianna Baptista (2011), refletindo também sobre o ato de tradução como possibilidade de abertura a outras culturas.</p>

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19

Wrobel, Norma, Bernhard Witulski, Dieter Schollmeyer, and Heiner Detert. "5,11-Dimethyl-6,12-dimethoxyindolo[3,2-b]carbazole." Acta Crystallographica Section E Structure Reports Online 69, no. 2 (2013): o255. http://dx.doi.org/10.1107/s1600536813001463.

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The title compound, C22H20N2O2, was prepared in a twofold Cadogan cyclization followed by doubleN-methylation. The crystal structure is characterized by a zigzag arrangement of centrosymmetric molecules. The indolocarbazole framework is essentially planar [maximum deviation = 0.028 (2) Å] and the methoxy groups are orthogonal to this plane [C—C—O—C torsion angle = −88.2 (2)°]. The lengths of the C—N bonds are nearly identical and all C—C bonds of the pyrrole subunit are significantly longer than the C—C bonds in the benzene rings.

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20

Gong, Peng, Leijiao Li, Jingbo Sun, Pengchong Xue та Ran Lu. "Synthesis of π-extended N-fused heteroacenes via regioselective Cadogan reaction". Tetrahedron Letters 57, № 13 (2016): 1468–72. http://dx.doi.org/10.1016/j.tetlet.2016.02.067.

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21

Limbach, Daniel, Mario Geffe, and Heiner Detert. "Synthesis of Carbolines via Microwave-Assisted Cadogan Reactions of Aryl-Nitropyridines." ChemistrySelect 3, no. 1 (2018): 249–52. http://dx.doi.org/10.1002/slct.201702964.

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22

Benzi, Alice, Lara Bianchi, Massimo Maccagno, Angela Pagano, Giovanni Petrillo, and Cinzia Tavani. "Sequential Annulations to Interesting Novel Pyrrolo[3,2-c]carbazoles." Molecules 24, no. 20 (2019): 3802. http://dx.doi.org/10.3390/molecules24203802.

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Herein we report a significant, valuable extension of a recently implemented pyrrole benzannulation methodology that, employing versatile nitrodienes from our lab as useful C4 building blocks, led to indole derivatives characterized by unusual patterns of substitution. The 6-nitro-7-arylindoles resulting from suitably derivatized, non-symmetric dienes are of foreseeable synthetic interest in search for new polyheterocyclic systems. As an example, pyrrolocarbazoles with a rarely reported ring fusion were synthesized with the classical Cadogan protocol. Furthermore, the proven easy reducibility

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23

Anderson, Martin. "London, Cadogan Hall and King's Place: Second London Festival of Bulgarian Culture." Tempo 67, no. 265 (2013): 81–83. http://dx.doi.org/10.1017/s0040298213000557.

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One of the most enjoyable characteristics of London musical life is that it is peopled by a generous number of foreigners who, every so often, take it upon themselves to enlighten the rest of us as to the music we are missing from back home. These can, of course, be hit-and-miss occasions, but it's in the nature of exploring unknown music of any age that you will happily put up with a handful of duds if you come away with a real discovery ringing in your ears. The Second London Festival of Bulgarian Culture (I seem to have missed the First) ran in various venues over the course of November 201

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24

Dunn, P. M. "Dr William Cadogan (1711-1797) of Bristol and the management of infants." Archives of Disease in Childhood 67, no. 1 Spec No (1992): 72–73. http://dx.doi.org/10.1136/adc.67.1_spec_no.72.

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25

Rigdon, Edward E. "Lee, Cadogan, and Chamberlain: an excellent point . . . But what about that iceberg?" AMS Review 3, no. 1 (2013): 24–29. http://dx.doi.org/10.1007/s13162-013-0034-0.

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26

Diamantopoulos, Adamantios. "MIMIC models and formative measurement: some thoughts on Lee, Cadogan & Chamberlain." AMS Review 3, no. 1 (2013): 30–37. http://dx.doi.org/10.1007/s13162-013-0035-z.

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27

Duffy, Matilda, Mara Di Filippo, and Marcus Baumann. "Synthesis of 2H-indazoles via the Cadogan reaction in batch and flow mode." Tetrahedron Letters 86 (December 2021): 153522. http://dx.doi.org/10.1016/j.tetlet.2021.153522.

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28

Bouchard, Jimmy, Salem Wakim, and Mario Leclerc. "Synthesis of Diindolocarbazoles by Cadogan Reaction: Route to Ladder Oligo(p-aniline)s." Journal of Organic Chemistry 69, no. 17 (2004): 5705–11. http://dx.doi.org/10.1021/jo049419o.

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29

Genung, Nathan E., Liuqing Wei, and Gary E. Aspnes. "Regioselective Synthesis of 2H-Indazoles Using a Mild, One-Pot Condensation–Cadogan Reductive Cyclization." Organic Letters 16, no. 11 (2014): 3114–17. http://dx.doi.org/10.1021/ol5012423.

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30

Neville, Peter. "Sir Alexander Cadogan and Lord Halifax's ‘Damascus road’ conversion over the Godesberg terms 1938." Diplomacy & Statecraft 11, no. 3 (2000): 81–90. http://dx.doi.org/10.1080/09592290008406171.

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31

Zhu, Jie S., Clarabella J. Li, Ka Yi Tsui, et al. "Accessing Multiple Classes of 2H-Indazoles: Mechanistic Implications for the Cadogan and Davis–Beirut Reactions." Journal of the American Chemical Society 141, no. 15 (2019): 6247–53. http://dx.doi.org/10.1021/jacs.8b13481.

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32

Nykaza, Trevor V., Antonio Ramirez, Tyler S. Harrison, Michael R. Luzung, and Alexander T. Radosevich. "Biphilic Organophosphorus-Catalyzed Intramolecular Csp2–H Amination: Evidence for a Nitrenoid in Catalytic Cadogan Cyclizations." Journal of the American Chemical Society 140, no. 8 (2018): 3103–13. http://dx.doi.org/10.1021/jacs.7b13803.

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33

Howell, Roy D. "Conceptual clarity in measurement—Constructs, composites, and causes: a commentary on Lee, Cadogan and Chamberlain." AMS Review 3, no. 1 (2013): 18–23. http://dx.doi.org/10.1007/s13162-013-0036-y.

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34

Yamamoto, Yoshishiko, Erina Ohkubo, and Masatoshi Shibuya. "Synthesis of 3-Aryl-2-(trifluoromethyl)indoles via Copper-Catalyzed Hydroarylation and Subsequent Cadogan Cyclization." Advanced Synthesis & Catalysis 359, no. 10 (2017): 1747–51. http://dx.doi.org/10.1002/adsc.201700122.

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35

Macera, Andrea Pereira, and André Torres Urdan. "Orientação para o mercado externo: teste de um modelo no Brasil e sua aplicação a uma amostra de empresas exportadoras brasileiras." Revista de Administração Contemporânea 8, no. 2 (2004): 95–115. http://dx.doi.org/10.1590/s1415-65552004000200006.

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Este artigo buscou investigar a Orientação para o Mercado Externo de uma amostra de empresas exportadoras brasileiras. Aplicou-se a escala multi-itens proposta por Cadogan et al. (1999) no Brasil, verificando-se seu ajustamento. Os resultados mostraram que esta pode ser considerada satisfatória quanto à: a) fidedignidade (a escala deve produzir resultados consistentes em medições repetidas); b) dimensionalidade (a Orientação para o Mercado Externo tem quatro dimensões); c) validade convergente (alta correlação entre medidas diferentes de um constructo). Contudo, a validade discriminante foi pa

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36

Dolbier,, William R., Yi-An Zhai, Will Wheelus, Merle A. Battiste, Ion Ghiviriga, and Michael D. Bartberger. "Remarkable Efficiency of the Aryne Chemistry of (Dehydro)octafluoro[2.2]paracyclophane When Using the Cadogan Method." Journal of Organic Chemistry 72, no. 2 (2007): 550–58. http://dx.doi.org/10.1021/jo0620009.

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37

Nykaza, Trevor V., Tyler S. Harrison, Avipsa Ghosh, Rachel A. Putnik, and Alexander T. Radosevich. "A Biphilic Phosphetane Catalyzes N–N Bond-Forming Cadogan Heterocyclization via PIII/PV═O Redox Cycling." Journal of the American Chemical Society 139, no. 20 (2017): 6839–42. http://dx.doi.org/10.1021/jacs.7b03260.

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38

Kim, Hyeong Seok, Deuk-young Goo, and Sang Kook Woo. "Efficient synthesis of aryl-substituted carbazoles via tandem double or triple suzuki coupling and cadogan cyclization." Tetrahedron 73, no. 11 (2017): 1413–23. http://dx.doi.org/10.1016/j.tet.2017.01.038.

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39

Genung, Nathan E., Liuqing Wei, and Gary E. Aspnes. "ChemInform Abstract: Regioselective Synthesis of 2H-Indazoles Using a Mild, One-Pot Condensation-Cadogan Reductive Cyclization." ChemInform 45, no. 49 (2014): no. http://dx.doi.org/10.1002/chin.201449125.

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40

Vogt, Astrid, Florian Henne, Christoph Wetzel, Elena Mena-Osteritz, and Peter Bäuerle. "Synthesis and characterization of S,N-heterotetracenes." Beilstein Journal of Organic Chemistry 16 (October 26, 2020): 2636–44. http://dx.doi.org/10.3762/bjoc.16.214.

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The synthesis and optoelectronic properties of novel S,N-heterotetracenes consisting of fused heterocyclic thiophene and pyrrole rings are presented. Tetracyclic and benzannulated derivatives with a varying number and sequence of sulfur and nitrogen heteroatoms were synthesized in multistep synthetic routes. A Buchwald–Hartwig amination of brominated precursors, thermolysis of azide precursors, and a Cadogan reaction of nitro-substituted precursors were successfully applied to eventually build-up pyrrole rings to stable and soluble fused systems. The various obtained heteroatom sequences ‘SSNS

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41

Li, Gongchun, Wei Wang, Chun Zhan, and Shengqiang Xiao. "Synthesis and properties of a novel decacyclic S,N-heteroacene." Acta Crystallographica Section C Structural Chemistry 78, no. 4 (2022): 250–56. http://dx.doi.org/10.1107/s2053229622003291.

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S,N-Heteroacene materials with fused multicyclic heteroaromatics have become increasingly attractive for organic optoelectronic device applications. In this work, the Cadogan ring-closure reaction between the benzene moiety of thieno[3,2-b]indole and 5,6-dinitrobenzo[c][1,2,5]thiadiazole was employed to prepare the novel decacyclic S,N-heteroacene 15,16-dibutyl-14,17-didodecyldithieno[2′′,3′′:2′,3′]indolo[6′,7′:4,5]pyrrolo[3,2-e:2′,3′-g][2,1,3]benzothiadiazole (TIP), C58H76N6S3. The conjugated backbone of TIP is extended in comparison with its octacyclic analogue as the central unit within Y6-

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42

Cruickshanks, Eveline. "Walpole's Tax On Catholics." Recusant History 28, no. 1 (2006): 95–102. http://dx.doi.org/10.1017/s0034193200011079.

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General Cadogan, who had succeeded the Duke of Marlborough as commander-in-chief of the Army asked for an increase of 10,000 men in the armed forces, after the discovery of the Atterbury Plot in 1722. Robert Walpole knew that additional taxation for the standing army was unpopular in Parliament and in the country at large. He, therefore, decided to impose a tax of £100,000 on Catholics to pay for it. This was over and above the double land tax which Catholics and Protestant Nonjurors had paid since 1689. The land tax at the time stood at 4s in the pound. The Atterbury Plot was a Tory Anglican

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43

Dehaen, Wim, Prasad Appukkuttan, and Erik Van der Eycken. "Microwave-Enhanced Cadogan Cyclization: An Easy Access to the 2-Substituted Carbazoles and other Fused Heterocyclic Systems." Synlett 2005, no. 01 (2004): 127–33. http://dx.doi.org/10.1055/s-2004-836030.

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44

Seymour, M. P., I. W. Duncan, T. M. Jefferies, and L. J. Notarianni. "Clean-up and separation of chlorobiphenyl isomers after synthesis by cadogan coupling using preparative high-performance liquid chromatography." Journal of Chromatography A 368 (January 1986): 174–79. http://dx.doi.org/10.1016/s0021-9673(00)91060-4.

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45

Irgashev, Roman A., Arseny A. Karmatsky, Pavel A. Slepukhin, Gennady L. Rusinov, and Valery N. Charushin. "A convenient approach to the design and synthesis of indolo[3,2-c]coumarins via the microwave-assisted Cadogan reaction." Tetrahedron Letters 54, no. 42 (2013): 5734–38. http://dx.doi.org/10.1016/j.tetlet.2013.08.030.

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46

Gibbert, Michael, Francesca Golfetto, and Fabrizio Zerbini. "What do we mean by “marketing” resources and competencies? A comment on Hooley, Greenley, Cadogan, and Fahey (JBR 2005)." Journal of Business Research 59, no. 1 (2006): 148–51. http://dx.doi.org/10.1016/j.jbusres.2005.03.001.

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47

Yamamoto, Yoshihiko, Satoshi Yamada, and Hisao Nishiyama. "Synthesis of 3-Arylindole-2-carboxylates via Copper-Catalyzed Hydroarylation of o-Nitrophenyl-Substituted Alkynoates and Subsequent Cadogan Cyclization." Advanced Synthesis & Catalysis 353, no. 5 (2011): 701–6. http://dx.doi.org/10.1002/adsc.201000858.

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48

Temme, Dirk, and Adamantios Diamantopoulos. "Higher-order models with reflective indicators." Journal of Modelling in Management 11, no. 1 (2016): 180–88. http://dx.doi.org/10.1108/jm2-05-2014-0037.

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Purpose – Higher-order factor models have recently been dismissed as a ‘misleading’, ‘meaningless’, and ‘needless’ approach for modeling multidimensional constructs (Lee and Cadogan, 2013; L & C, 2013 hereafter). The purpose of this paper is to show that – in contrast to L & C’s (2013) verdict – higher-order factor models are still a legitimate operationalization option for multidimensional constructs. Design/methodology/approach – Basic conceptual and statistical premises of L & C’s (2013) arguments against higher-order factor models are scrutinized both conceptually and statistic

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49

Laing, Simon. "Emergency Medicine (6th edn)Anthony FT Brown Michael D Cadogan Hodder Arnold 2011 £21.99. 532 978 1 444 12013 4." British Journal of Hospital Medicine 73, no. 8 (2012): 477. http://dx.doi.org/10.12968/hmed.2012.73.8.477.

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50

Creencia, Evelyn Cuevas, Masahiro Kosaka, Toshikatsu Muramatsu, Masashi Kobayashi, Tomohiro Iizuka, and Takaaki Horaguchi. "Microwave-assisted Cadogan reaction for the synthesis of 2-aryl-2H-indazoles, 2-aryl-1H-benzimidazoles, 2-carbonylindoles, carbazole, and phenazine." Journal of Heterocyclic Chemistry 46, no. 6 (2009): 1309–17. http://dx.doi.org/10.1002/jhet.267.

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