Relevant bibliographies by topics / Haloarens

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Haloarens'

Author: Grafiati
Published: 5 June 2025
Last updated: 2 August 2025

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Journal articles on the topic "Haloarens"

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Nocera, Giuseppe, and John A. Murphy. "Ground State Cross-Coupling of Haloarenes with Arenes Initiated by Organic Electron Donors, Formed in situ: An Overview." Synthesis 52, no. 03 (2019): 327–36. http://dx.doi.org/10.1055/s-0039-1690614.

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Many reactions have been discovered that lead to coupling of haloarenes to arenes using potassium tert-butoxide as the base, and one of a variety of organic compounds as an additive. The organic additive reacts with the base to form a strong organic electron donor in situ that initiates a base-induced homolytic aromatic substitution (BHAS) coupling reaction, by converting the haloarene into an aryl radical. This brief report presents an overview of the wide range of organic additives that can be used, and the organic electron donors that they form.
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Saberov, Vagiz Sh, Daniel A. Evans, Nikolai I. Korotkikh, et al. "Exceptionally efficient catalytic hydrodechlorination of persistent organic pollutants: application of new sterically shielded palladium carbene complexes." Dalton Trans. 43, no. 48 (2014): 18117–22. http://dx.doi.org/10.1039/c4dt02908a.

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Nozawa-Kumada, Kanako, Yuki Iwakawa, So Onuma, Masanori Shigeno, and Yoshinori Kondo. "NaH-mediated direct C–H arylation in the presence of 1,10-phenanthroline." Chemical Communications 56, no. 56 (2020): 7773–76. http://dx.doi.org/10.1039/d0cc00730g.

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Del Grosso, Alessandro, Josue Ayuso Carrillo, and Michael J. Ingleson. "Regioselective electrophilic borylation of haloarenes." Chemical Communications 51, no. 14 (2015): 2878–81. http://dx.doi.org/10.1039/c4cc10153g.

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Bzeih, Tourin, Timothée Naret, Ali Hachem, et al. "A general synthesis of arylindoles and (1-arylvinyl)carbazoles via a one-pot reaction from N-tosylhydrazones and 2-nitro-haloarenes and their potential application to colon cancer." Chemical Communications 52, no. 88 (2016): 13027–30. http://dx.doi.org/10.1039/c6cc07666a.

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Konishi, Hideyuki, Hiroki Nagase, and Kei Manabe. "Concise synthesis of cyclic carbonyl compounds from haloarenes using phenyl formate as the carbonyl source." Chemical Communications 51, no. 10 (2015): 1854–57. http://dx.doi.org/10.1039/c4cc09413a.

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Hassan, Mohamed E. "Palladium catalyzed coupling reaction for the synthesis of C-5 aryl and heteroaryl substituted 2’-deoxycytidine." Collection of Czechoslovak Chemical Communications 56, no. 6 (1991): 1295–99. http://dx.doi.org/10.1135/cccc19911295.

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Cytosine nucleosides substituted at C-5 with differently substituted aryls and heteroaryls have been prepared via a palladium catalyzed reaction utilizing 5-chloromercuri or acetoxymercuri nucleosides and haloarenes or heteroarenes.
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Mahmood, Qaiser, Erlin Yue, Wenjuan Zhang, Gregory A. Solan, Tongling Liang, and Wen-Hua Sun. "Bisimino-functionalized dibenzo[a,c]acridines as highly conjugated pincer frameworks for palladium(ii): synthesis, characterization and catalytic performance in Heck coupling." Organic Chemistry Frontiers 3, no. 12 (2016): 1668–79. http://dx.doi.org/10.1039/c6qo00469e.

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The NNC-Pd pincer complexes, systematically derived from phenanthrene-9,10-dione, are able to efficiently mediate the coupling of haloarenes with vinyl-containing substrates (up to TON = 174 000) with a broad substrate scope.
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Favier, Isabelle, Marie-Lou Toro, Pierre Lecante, Daniel Pla, and Montserrat Gómez. "Palladium-mediated radical homocoupling reactions: a surface catalytic insight." Catalysis Science & Technology 8, no. 18 (2018): 4766–73. http://dx.doi.org/10.1039/c8cy00901e.

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In this work, we report a palladium nanoparticle-promoted reductive homocoupling of haloarenes, exhibiting a broad functional group tolerance. A mechanistic study was carried out, suggesting single-electron transfer processes on the metal surface.
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Emery, Katie J., Tell Tuttle, and John A. Murphy. "Evidence of single electron transfer from the enolate anion of an N,N′-dialkyldiketopiperazine additive in BHAS coupling reactions." Org. Biomol. Chem. 15, no. 41 (2017): 8810–19. http://dx.doi.org/10.1039/c7ob02209c.

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A designed N,N′-dialkyldiketopiperazine (DKP) provides evidence for the role of DKP additives as initiators that act by electron transfer in base-induced homolytic aromatic substitution reactions, involving coupling of haloarenes to arenes.
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Dissertations / Theses on the topic "Haloarens"

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Gomez-Quero, Santiago. "The development of a catalytic process for the hydrotreatment of haloarenes." Thesis, Heriot-Watt University, 2009. http://hdl.handle.net/10399/2302.

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The abatement of halogenated compounds released from various processes into the environment is now recognized as a pressing environmental issue. Catalytic hydrodehalogenation (HDH) has emerged as a potential technology that can facilitate waste transformation and reuse. In this thesis, a comprehensive study of the critical reaction/catalyst variables is considered for the HDH of a range of haloarenes (chloroand bromo-phenols and chlorobenzenes) using (commercial) Pd/Al2O3 and (laboratory synthesised) Au supported on -Fe2O3 and Fe3O4. Aqueous phase (T = 303 K) HDH is demonstrated to be structu
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Che-WeiLee and 李哲維. "Palladium-Catalyzed Indenoannulation of Haloarenes with Diarylethynes: One-pot Synthesis, Structural Analysis and Properties of Fluorene Derivatives." Thesis, 2015. http://ndltd.ncl.edu.tw/handle/gmgcac.

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Book chapters on the topic "Haloarens"

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Yoon, T. P., and E. N. Jacobsen. "Cyanation/Hydrolysis of Haloarenes." 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-020-00524.

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Kauffman, M. C., and P. J. Walsh. "Aryl Additions Using Haloarenes." In Stereoselective Reactions of Carbonyl and Imino Groups. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-202-00226.

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Yoon, T. P., and E. N. Jacobsen. "Reductive Metalation of Haloarenes." 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-020-01208.

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Ulrich, H. "With Carbon Monoxide and Haloarenes." In Five-Membered Hetarenes with One Chalcogen and One Additional Heteroatom. Georg Thieme Verlag KG, 2002. http://dx.doi.org/10.1055/sos-sd-011-01037.

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Yoon, T. P., and E. N. Jacobsen. "Metal-Catalyzed Carboxylation of Haloarenes." 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-020-00523.

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Yoon, T. P., and E. N. Jacobsen. "Lithium–Halogen Exchange with Haloarenes." 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-020-01209.

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Evano, G. "Coupling of Haloarenes with Propynoic Acid." 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-020-00504.

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Griesbeck, A. G., and A. Soldevilla. "Synthesis from Haloarenes and Metal Alkynides." In Polyynes, Arynes, Enynes, and Alkynes. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-043-00309.

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Griesbeck, A. G., and A. Soldevilla. "Synthesis from Haloarenes and Terminal Alkynes." In Polyynes, Arynes, Enynes, and Alkynes. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-043-00317.

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Yoon, T. P., and E. N. Jacobsen. "Transition-Metal-Catalyzed Carbonylation of Haloarenes." 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-020-01215.

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Conference papers on the topic "Haloarens"

1

VO-THANH, Giang, and Alain PETIT. "Solvent-Free Microwaves Assisted Amination of Haloarenes by Aromatic Nucleophilic Substitution." In The 15th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2011. http://dx.doi.org/10.3390/ecsoc-15-00763.

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Journal articles
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