Добірка наукової літератури з теми "C-Hetero Bond"
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Статті в журналах з теми "C-Hetero Bond"
Zhao, Yating, and Wujiong Xia. "Photochemical C–H bond coupling for (hetero)aryl C(sp2)–C(sp3) bond construction." Organic & Biomolecular Chemistry 17, no. 20 (2019): 4951–63. http://dx.doi.org/10.1039/c9ob00244h.
Повний текст джерелаWei, Kai-Jie, Zheng-jun Quan, Zhang Zhang, Yu-xia Da, and Xi-cun Wang. "Direct C–H heteroarylation of azoles with 1,2-di(pyrimidin-2-yl)disulfides through C–S cleavage of disulfides." RSC Advances 6, no. 81 (2016): 78059–63. http://dx.doi.org/10.1039/c6ra18997k.
Повний текст джерелаRoth-Barton, Jesse, Yit Wooi Goh, Asimo Karnezis та Jonathan M. White. "Structural Studies on α-Pyrone Cycloadducts. Manifestation of the Early Stages of CO2 Extrusion by retro Hetero-Diels - Alder Reaction". Australian Journal of Chemistry 62, № 5 (2009): 407. http://dx.doi.org/10.1071/ch09018.
Повний текст джерелаCorrea, Arkaitz, та Marcos Segundo. "Cross-Dehydrogenative Coupling Reactions for the Functionalization of α-Amino Acid Derivatives and Peptides". Synthesis 50, № 15 (25 червня 2018): 2853–66. http://dx.doi.org/10.1055/s-0037-1610073.
Повний текст джерелаYang, Tao, Congshan Zhou, Zan Yang, Jiao Li, Jie Hua та Jianmin Yi. "KI/K2S2O8-Mediated α-C–H Sulfenylation of Carbonyl Compounds with (Hetero)Aryl Thiols". Synlett 28, № 17 (13 липня 2017): 2325–29. http://dx.doi.org/10.1055/s-0036-1588483.
Повний текст джерелаZhang, Zuxiao, Leah M. Stateman та David A. Nagib. "δ C–H (hetero)arylationviaCu-catalyzed radical relay". Chemical Science 10, № 4 (2019): 1207–11. http://dx.doi.org/10.1039/c8sc04366c.
Повний текст джерелаKnochel, Paul, Maximilian Hofmayer, Jeffrey Hammann, and Gérard Cahiez. "Iron-Catalyzed C(sp2)–C(sp3) Cross-Coupling Reactions of Di(hetero)arylmanganese Reagents and Primary and Secondary Alkyl Halides." Synlett 29, no. 01 (August 30, 2017): 65–70. http://dx.doi.org/10.1055/s-0036-1590891.
Повний текст джерелаIrgashev, Roman A., Arseny A. Karmatsky, Gennady L. Rusinov, and Valery N. Charushin. "A new and convenient synthetic way to 2-substituted thieno[2,3-b]indoles." Beilstein Journal of Organic Chemistry 11 (June 11, 2015): 1000–1007. http://dx.doi.org/10.3762/bjoc.11.112.
Повний текст джерелаGe, Danhua, and Xue-Qiang Chu. "Multiple-fold C–F bond functionalization for the synthesis of (hetero)cyclic compounds: fluorine as a detachable chemical handle." Organic Chemistry Frontiers 9, no. 7 (2022): 2013–55. http://dx.doi.org/10.1039/d1qo01749g.
Повний текст джерелаChupakhin, O. N., A. V. Shchepochkin, and V. N. Charushin. "Atom- and step-economical nucleophilic arylation of azaaromatics via electrochemical oxidative cross C–C coupling reactions." Green Chemistry 19, no. 13 (2017): 2931–35. http://dx.doi.org/10.1039/c7gc00789b.
Повний текст джерелаДисертації з теми "C-Hetero Bond"
Subba, Raju. "Studies on the reactions of C - hetero bond formation." Thesis, University of North Bengal, 2015. http://ir.nbu.ac.in/handle/123456789/1854.
Повний текст джерелаSaha, Bittu. "Development of Novel methodologies for the construction of c-hetero bond." Thesis, University of North Bengal, 2018. http://ir.nbu.ac.in/handle/123456789/2823.
Повний текст джерелаLi, Haoran. "Pd-catalyzed C-H bond functionalizations of (hetero)arenes and alkenes : A one step access to poly(hetero)aromatics and styrene derivatives." Thesis, Rennes, Ecole nationale supérieure de chimie, 2020. http://www.theses.fr/2020ENCR0068.
Повний текст джерелаIn order to explain the background of my research work, in the first chapter, I summarized general mechanistic information on palladium-catalyzed C-H bond arylation and detailed some literature on direct arylation related to my research work. My objectives were to study the reactivity of new synthetic units allowing the straightforward access to bi-(hetero)aryls compounds or styrene derivatives using aryl halides or benzenesulfonyl chloride derivatives as the aryl-sources. Then, in the chapters 2-6, I summarized my research work. I studied the regiocontrolled palladium-catalyzed direct C2-arylations of Methoxsalen using benzenesulfonyl chlorides and C2,C3-diarylations using aryl bromides as the aryl sources. These results are summarized in the chapter 2. Then, I found that Pd-catalyzed direct arylation reaction allows the easy access to Ticlopidine derivatives arylated at the C5-position of the thienyl ring in one step. These results are reported in the chapter 3. In the chapter 4, we studied the reactivity of Diflufenican which contains a 1,3-difluorobenzene ring and a pyridine unit using Ru and Pd catalysis. Under appropriate conditions, two different C-H bonds of Diflufenican could be arylated. In the chapter 5, I employed different aryl sources to functionalize the C10- and C11-positions of dibenzo[b,f]azepines, and obtained asymmetric products. Through these reactions, a wide diversity of functional group were introduced on the dibenzo[b,f]azepine derivatives. Finally, in the Chapter 6, I report the first method allowing to prepare C10-arylated Cyproheptadine derivatives
Zhao, Liqin. "Palladium-catalyzed direct arylation via sp² and sp³ C-H activation of hetero(aromatics) and hydrocarbons for C-C bond formation." Thesis, Rennes 1, 2014. http://www.theses.fr/2014REN1S038/document.
Повний текст джерелаDuring this thesis, we were interested in the sp² and sp³ C-H bond activation catalyzed by palladium catalysts for the preparation of (hetero)aryl-aryls and biaryls. This method is considered as cost effective and environmentally attractive compared to the classical couplings such as Suzuki, Heck, or Negishi. First we described the palladium-catalyzed direct C2-arylation of benzothiophene in the absence of phosphine ligand with high selectivity. We also demonstrated that it is possible to active both C2 and C5 C-H bonds for access to 2,5-diarylated compounds in one step, and also to non-symmetrically substituted 2,5-diarylpyrroles via sequential C2 arylation followed by C5 arylation. We also studied the reactivity of polychlorobenzenes via palladium-catalyzed C-H activation. We finally examined the palladium-catalysed selective sp² and sp³ C-H bond activation of guaiazulene. The selectivity depends on the solvent and base: sp² C2-arylation (KOAc in ethylbenzene), sp² C3-arylation (KOAc in DMAc) and sp³ C4-Me arylation (CsOAc/K₂CO₃ in DMAc). Through this method, a challenging sp³ C-H bond was activated
Potukuchi, Harish Kumar [Verfasser], Lutz [Akademischer Betreuer] Ackermann, and Dietmar [Akademischer Betreuer] Stalke. "Catalytic syntheses and copper- or ruthenium-catalyzed direct C H bond arylations of (hetero)arenes / Harish Kumar Potukuchi. Gutachter: Lutz Ackermann ; Dietmar Stalke. Betreuer: Lutz Ackermann." Göttingen : Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2011. http://d-nb.info/1043939148/34.
Повний текст джерелаPotukuchi, Harish Kumar. "Catalytic syntheses and copper- or ruthenium-catalyzed direct C H bond arylations of (hetero)arenes." Doctoral thesis, 2011. http://hdl.handle.net/11858/00-1735-0000-0006-B0A3-7.
Повний текст джерелаFenner, Sabine. "Sustainable Strategies for Site-Selective C−VC Bond Formations through Direct C−H Bond Functionalizations." Doctoral thesis, 2012. http://hdl.handle.net/11858/00-1735-0000-0006-B090-4.
Повний текст джерелаRokade, Balaji Vasantrao. "Copper-Catalyzed Novel Oxidative Transformations : Construction of Carbon-Hetero Bonds." Thesis, 2014. http://etd.iisc.ac.in/handle/2005/3479.
Повний текст джерелаRokade, Balaji Vasantrao. "Copper-Catalyzed Novel Oxidative Transformations : Construction of Carbon-Hetero Bonds." Thesis, 2014. http://etd.iisc.ernet.in/2005/3479.
Повний текст джерелаRao, Santhosh. "Molecular Construction Using Carbene and Diboron Systems: Catalytic Transformation of C-C and C-Hetero Atom Bonds." Thesis, 2018. https://etd.iisc.ac.in/handle/2005/5327.
Повний текст джерелаЧастини книг з теми "C-Hetero Bond"
Gupta, Aniket, Sreedhar Gundekari, and Sukalyan Bhadra. "C(sp3)–H Bond Hetero-functionalization of Aliphatic Carboxylic Acid Equivalents Enabled by Transition Metals." In Catalysis for Clean Energy and Environmental Sustainability, 383–427. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-65017-9_13.
Повний текст джерелаWong, Shun-Man, and Fuk-Yee Kwong. "Nondirected C H Bond Functionalizations of (Hetero)arenes." In Strategies for Palladium-Catalyzed Non-Directed and Directed C-H Bond Functionalization, 49–166. Elsevier, 2017. http://dx.doi.org/10.1016/b978-0-12-805254-9.00003-7.
Повний текст джерелаSoni, Vineeta, and Benudhar Punji. "Palladacycles for Directed and Nondirected C H Bond Functionalization of (Hetero)arenes." In Strategies for Palladium-Catalyzed Non-Directed and Directed C-H Bond Functionalization, 357–415. Elsevier, 2017. http://dx.doi.org/10.1016/b978-0-12-805254-9.00010-4.
Повний текст джерелаKumar, Chandan. "The Synthesis, Spectral and Antimicrobial Study of Heterobinuclear Complexes of Copper (II) Schiff Base with Alkali Metals Salts." In Progress in Chemical and Biological Science, 28–33. Lincoln University College, Malaysia, 2023. http://dx.doi.org/10.31674/book.2023pcbs004.
Повний текст джерелаShang, Y., Y. Ren, and W. Su. "1.6 Copper-Catalyzed Acidic C—H Functionalization." In Base-Metal Catalysis 1. Stuttgart: Georg Thieme Verlag KG, 2023. http://dx.doi.org/10.1055/sos-sd-238-00106.
Повний текст джерелаBałczewski, Piotr, and Krzysztof Owsianik. "Quinquevalent phosphorus acids." In Organophosphorus Chemistry, 109–231. Royal Society of Chemistry, 2024. http://dx.doi.org/10.1039/bk9781837672738-00109.
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