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Relevant bibliographies by topics / Arenediazonium salts

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Dissertations / Theses
Book chapters

Academic literature on the topic 'Arenediazonium salts'

Author: Grafiati

Published: 4 June 2021

Last updated: 6 February 2022

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Journal articles on the topic "Arenediazonium salts"

1

Sengupta, Saumitra, and Srinivasan Chandrasekaran. "Modifications of amino acids using arenediazonium salts." Organic & Biomolecular Chemistry 17, no. 36 (2019): 8308–29. http://dx.doi.org/10.1039/c9ob01471c.

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Aryl transfer reactions from arenediazonium salts have started to make their impact in chemical biology with initial forays in the arena of arylative modifications and bio-conjugations of amino acids, peptides and proteins.

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2

Pahovnik, David, Uroš Uršič, Uroš Grošelj, Anton Meden, Jurij Svete, and Branko Stanovnik. "Synthesis of Dimethyl 1-(Hetero)aryl-4-oxo-1,4-dihydropyridazine- 3,5-dicarboxylates from Dimethyl 3-Oxopentane-1,5-dioates." Zeitschrift für Naturforschung B 63, no. 4 (2008): 407–14. http://dx.doi.org/10.1515/znb-2008-0407.

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AbstractDimethyl 3-oxopentane-1,5-dioate (dimethyl acetone-1,3-dicarboxylate) (1) was transformed first with (hetero)arenediazonium salts 3a - j into dimethyl 2-[(hetero)arylhydrazono]pentane-1,5-dioates 4a - j followed by reaction with N,N-dimethylformamide dimethylacetal (DMFDMA) to afford, without isolation of intermediates 5a - j, dimethyl 1-(hetero)aryl-4-oxo-1,4-dihydropyridazine-3,5- dicarboxylates 6a - j. An alternative method represents transformation of 1 with DMFDMA into dimethyl 2-[(dimethylamino)methylidene]-3-oxopentane-1,5-dioate (7) followed by treatment with (hetero)arenediazo

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3

Felpin, François-Xavier, and Saumitra Sengupta. "Biaryl synthesis with arenediazonium salts: cross-coupling, CH-arylation and annulation reactions." Chemical Society Reviews 48, no. 4 (2019): 1150–93. http://dx.doi.org/10.1039/c8cs00453f.

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4

Wang, Xiaojun, Yajun Li, Yuwei Guo, Zhentong Zhu, Yongming Wu, and Weiguo Cao. "Direct isoperfluoropropylation of arenediazonium salts with hexafluoropropylene." Organic Chemistry Frontiers 3, no. 3 (2016): 304–8. http://dx.doi.org/10.1039/c5qo00388a.

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Perfluoropropylene can be used directly for isoperfluoropropylation of arenediazonium salts in the presence of silver fluoride and cuprous iodide. A practical tandem diazotization and isoperfluoropropylation protocol was developed for aniline derivatives to generate isoperfluoropropylarenes with good functional-group compatibility.

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Lampard, Christopher, John A. Murphy, Faiza Rasheed, Norman Lewis, Michael B. Hursthouse, and D. E. Hibbs. "Novel synthetic applications of arenediazonium salts." Tetrahedron Letters 35, no. 46 (1994): 8675–78. http://dx.doi.org/10.1016/s0040-4039(00)78469-3.

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6

Koizumi, Toshio, Nadeem Bashir, and John A. Murphy. "Reactions of Arenediazonium Salts with Diazadithiafulvalenes." Tetrahedron Letters 38, no. 43 (1997): 7635–38. http://dx.doi.org/10.1016/s0040-4039(97)01813-3.

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Fabrizi, Giancarlo, Antonella Goggiamani, Alessio Sferrazza, and Sandro Cacchi. "Sonogashira Cross-Coupling of Arenediazonium Salts." Angewandte Chemie 122, no. 24 (2010): 4161–64. http://dx.doi.org/10.1002/ange.201000472.

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Fabrizi, Giancarlo, Antonella Goggiamani, Alessio Sferrazza, and Sandro Cacchi. "Sonogashira Cross-Coupling of Arenediazonium Salts." Angewandte Chemie International Edition 49, no. 24 (2010): 4067–70. http://dx.doi.org/10.1002/anie.201000472.

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Matheis, Christian, Kévin Jouvin, and Lukas J. Goossen. "Sandmeyer Difluoromethylation of (Hetero-)Arenediazonium Salts." Organic Letters 16, no. 22 (2014): 5984–87. http://dx.doi.org/10.1021/ol5030037.

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10

Gracza, Tibor, Zdeněk Arnold, and Jaroslav Kováč. "Electrophilic ipso substitutions of furan vinamidinium salts." Collection of Czechoslovak Chemical Communications 53, no. 5 (1988): 1053–59. http://dx.doi.org/10.1135/cccc19881053.

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5-(N,N-Dialkylamino)-2-furfurylidene-N,N-dialkylimminium salts I (the vinamidinium salts of furan) react with arenediazonium salts to give products of ipso substitution in position 2 of the furan ring, i.e. 5-(N,N-dialkylamino)-2-azoarenefuran salts II. The structure of these products was evidenced by 1H NMR and UV spectral data.

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Dissertations / Theses on the topic "Arenediazonium salts"

1

Le, Strat Franck. "Electroreductive cyclisations of arenediazonium salts." Thesis, University of Strathclyde, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.273906.

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Canning, Peter Sebastian John. "Dediazoniation of arenediazonium salts as a route to fluoroarenes." Thesis, University of Newcastle Upon Tyne, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.311135.

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McCrudden, Katherine. "A kinetics and product analytical study of the solvolysis of arenediazonium ions." Thesis, University of Newcastle Upon Tyne, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.260871.

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Rasheed, Faiza. "Electron transfer reactions of tetrathiafulvalene." Thesis, University of Nottingham, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.294254.

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Felipe-Blanco, Diego. "Salicylic Acid-Catalyzed Radical Arylations from In-situ Formed Arenediazonium Salts." Doctoral thesis, Universidad de Alicante, 2020. http://hdl.handle.net/10045/112757.

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In this thesis, it has been studied the deamination of aromatic amines, through in situ formed diazonium salts as reaction intermediates, catalyzed by salicylic acid, a nontoxic, eco-friendly and economic catalyst. In the early part of the thesis (Chapter I) it has studied the deamination process using THF as solvent as hydrogen donor and anilines as radical source, to carry the hydrodeamination reaction, as well as the process in its deuterodeamination manner using deuterated solvent. Following with this study in Chapter II and Chapter III, it has been studied the addition of the aromatic rad

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Garcia, Ariel Lazaro Llanes. "Reação de arilação de Heck com sais de arenodiazonio : aplicações nas sinteses totais de prolinas e pirrolidinas poliidroxiladas, rolipram e analogos do baclofeno, e na sintese formal de prepolicitrina A e policitrina A." [s.n.], 2008. http://repositorio.unicamp.br/jspui/handle/REPOSIP/248358.

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Orientador: Carlos Roque Duarte Correia<br>Acompanha Anexo denominado V.2. Paginação continua<br>Tese (doutorado) - Universidade Estadual de Campinas, Instituto de Quimica<br>Made available in DSpace on 2018-08-12T12:04:47Z (GMT). No. of bitstreams: 1 Garcia_ArielLazaroLlanes_D.pdf: 15520800 bytes, checksum: 2744757a92f3045d187a1c68320729d5 (MD5) Previous issue date: 2008<br>Resumo: A reação de arilação de Heck-Matsuda é um procedimento sintético valioso e extremamente versátil para a formação de ligações carbono-carbono, baseada no acoplamento de uma olefina com um sal de arenodiazônio na p

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Azambuja, Francisco de 1986. "Estudo e aplicação sintetica da arilação de Heck-Matsuda de desidrohidroxi esteres e desidroamino esteres." [s.n.], 2010. http://repositorio.unicamp.br/jspui/handle/REPOSIP/249840.

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Orientador: Carlos Roque Duarte Correia<br>Dissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Quimica<br>Made available in DSpace on 2018-08-15T20:34:49Z (GMT). No. of bitstreams: 1 Azambuja_Franciscode_M.pdf: 6423668 bytes, checksum: 29069e3111714888aee628002e55cf0c (MD5) Previous issue date: 2010<br>Resumo: A arilação de acrilatos 2-acetóxi ou acetamido substituídos foi estudada utilizando a reação de Heck com sais de arenodiazônio. Após avaliação do catalisador, solvente, temperatura e acidez do meio reacional na arilação do 2-acetoxiacrilato de metila com o sal tetr

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Prediger, Patrícia 1984. "Reações de arilação de Heck com sais de arenodiazônio : estudos metodológicos e aplicações nas sínteses de compostos bioativos." [s.n.], 2012. http://repositorio.unicamp.br/jspui/handle/REPOSIP/249886.

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Orientador: Carlos Roque Duarte Correira<br>Tese (doutorado) - Universidade Estadual de Campinas, Instituto de Química<br>Made available in DSpace on 2018-08-20T23:15:33Z (GMT). No. of bitstreams: 1 Prediger_Patricia_D.pdf: 29103926 bytes, checksum: bd694717759d7b58fda99bfb77a7fa06 (MD5) Previous issue date: 2012<br>Resumo: O presente trabalho foi centrado na arilacao de Heck-Matuda de diferentes olefinas com sais de arenodiazonio e a aplicacao dos produtos arilados na sintese de compostos bioativos. O trabalho esta dividido em dois capitulos: 1) Reacoes de acoplamento de Heck-Matsuda entre

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Miranda, Karen Fabiane Canto. "Estudo da reação de Heck de anidridos maleicos com sais de arenodiazônio e suas aplicações sintéticas." [s.n.], 2010. http://repositorio.unicamp.br/jspui/handle/REPOSIP/249881.

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Orientador: Carlos Roque Duarte Correia<br>Tese (doutorado) - Universidade Estadual de Campinas, Instituto de Química<br>Made available in DSpace on 2018-08-17T04:40:41Z (GMT). No. of bitstreams: 1 Miranda_KarenFabianeCanto_D.pdf: 2096574 bytes, checksum: b7fd48d07ff428a29ed0b7b0b0c1ad8c (MD5) Previous issue date: 2010<br>Resumo: O primeiro capítulo deste trabalho concentra-se no estudo metodológico da reação de Heck com anidrido maleico empregando diversos sais de arenodiazônio. A reação foi investigada em diversas condições e, num primeiro momento, foi possível, utilizando acetato de palá

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Pastre, Júlio Cezar 1979. "Reações de Heck de acrilatos substituidos com sais de arenodiazonio em solventes organicos e liquidos ionicos. Aplicação na sintese da paroxetina, da nocaina, da indatralina e da sertralina." [s.n.], 2009. http://repositorio.unicamp.br/jspui/handle/REPOSIP/249878.

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Orientador: Carlos Roque Duarte Correia<br>Tese (doutorado) - Universidade Estadual de Campinas, Instituto de Quimica<br>Made available in DSpace on 2018-08-14T14:22:36Z (GMT). No. of bitstreams: 1 Pastre_JulioCezar_D.pdf: 10159507 bytes, checksum: 4f4f32c2c414df354e1d53179d9ebe18 (MD5) Previous issue date: 2009<br>Resumo: Neste trabalho, efetuou-se um estudo da reação de Heck de acrilatos substituídos com sais de arenodiazônio. Um protocolo estereosseletivo para a preparação de acrilatos b,b-diarilssubstituidos foi desenvolvido, baseando-se na arilação Heck do cinamato de metila com sais de

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Book chapters on the topic "Arenediazonium salts"

1

Yoon, T. P., and E. N. Jacobsen. "Carboxylation of Arenediazonium Salts." In Three Carbon-Heteroatom Bonds: Acid Halides; Carboxylic Acids and Acid Salts. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-020-00525.

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2

Alonso, D. A., and C. Nájera. "Arenediazonium Salts as Electrophiles." In Monocyclic Arenes, Quasiarenes, and Annulenes. Georg Thieme Verlag KG, 2010. http://dx.doi.org/10.1055/sos-sd-045-00177.

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3

Kitching, W., and M. Glenn. "Mercury Substitution of Arenediazonium Salts." In Compounds of Groups 12 and 11 (Zn, Cd, Hg, Cu, Ag, Au). Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-003-00221.

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4

Kikelj, D. "From Arenediazonium Salts and Nitriles." In Six-Membered Hetarenes with Two Identical Heteroatoms. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-016-00807.

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"Product Class 23: Arenediazonium Salts." In Science of Synthesis: Houben–Weyl Methods of Molecular Transformations, edited by Ramsden and Bellus. Georg Thieme Verlag, 2007. http://dx.doi.org/10.1055/sos-sd-031-01557.

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Keller, P. A. "Insertion of Carbon Monoxide into Arenediazonium Salts." In Three Carbon-Heteroatom Bonds: Acid Halides; Carboxylic Acids and Acid Salts. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-020-00633.

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7

Jung, N., and S. Bräse. "Reaction of Arenediazonium Salts with Primary Amines." In Nitro, Nitroso, Azo, Azoxy, and Diazonium Compounds, Azides, Triazenes, and Tetrazenes. Georg Thieme Verlag KG, 2010. http://dx.doi.org/10.1055/sos-sd-041-00578.

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8

Sapeta, K., and M. A. Kerr. "From [2-(Halomethyl)aryl]zincs and Arenediazonium Salts." In Science of Synthesis Knowledge Updates KU 2011/1. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-112-00015.

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Jung, N., and S. Bräse. "Reaction of Arenediazonium Salts with Diamines and Formaldehyde." In Nitro, Nitroso, Azo, Azoxy, and Diazonium Compounds, Azides, Triazenes, and Tetrazenes. Georg Thieme Verlag KG, 2010. http://dx.doi.org/10.1055/sos-sd-041-00594.

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Jung, N., and S. Bräse. "Reaction of Arenediazonium Salts with Primary Amines and Formaldehyde." In Nitro, Nitroso, Azo, Azoxy, and Diazonium Compounds, Azides, Triazenes, and Tetrazenes. Georg Thieme Verlag KG, 2010. http://dx.doi.org/10.1055/sos-sd-041-00593.

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