Gotowa bibliografia na temat „Carbon-hetero bond”
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Artykuły w czasopismach na temat "Carbon-hetero bond"
Larrosa, Igor, i Josep Cornella. "Decarboxylative Carbon-Carbon Bond-Forming Transformations of (Hetero)aromatic Carboxylic Acids". Synthesis 44, nr 05 (3.02.2012): 653–76. http://dx.doi.org/10.1055/s-0031-1289686.
Pełny tekst źródłaGu, Huoliang, Xiong Sun, Yong Wang, Haihong Wu i Peng Wu. "Highly efficient mesoporous polymer supported phosphine-gold(i) complex catalysts for amination of allylic alcohols and intramolecular cyclization reactions". RSC Advances 8, nr 4 (2018): 1737–43. http://dx.doi.org/10.1039/c7ra12498h.
Pełny tekst źródłaKataria, Meenal, Subhamay Pramanik, Navleen Kaur, Manoj Kumar i Vandana Bhalla. "Ferromagnetic α-Fe2O3 NPs: a potential catalyst in Sonogashira–Hagihara cross coupling and hetero-Diels–Alder reactions". Green Chemistry 18, nr 6 (2016): 1495–505. http://dx.doi.org/10.1039/c5gc02337h.
Pełny tekst źródłaCornella, Josep, i Igor Larrosa. "ChemInform Abstract: Decarboxylative Carbon-Carbon Bond-Forming Transformations of (Hetero)aromatic Carboxylic Acids". ChemInform 43, nr 19 (12.04.2012): no. http://dx.doi.org/10.1002/chin.201219252.
Pełny tekst źródłaD’Amato, Assunta, i Giorgio Della Sala. "Vinylogous and Arylogous Stereoselective Base-Promoted Phase-Transfer Catalysis". Catalysts 11, nr 12 (18.12.2021): 1545. http://dx.doi.org/10.3390/catal11121545.
Pełny tekst źródłaVogel, Pierre, i José Angel Sordo Gonzalo. "Expeditious Asymmetric Synthesis of Polypropionates Relying on Sulfur Dioxide-Induced C–C Bond Forming Reactions". Catalysts 11, nr 11 (21.10.2021): 1267. http://dx.doi.org/10.3390/catal11111267.
Pełny tekst źródłaCui, Luxia, Toshikazu Ono, Md Jakir Hossain i Yoshio Hisaeda. "Electrochemically driven, cobalt–carbon bond-mediated direct intramolecular cyclic and acyclic perfluoroalkylation of (hetero)arenes using X(CF2)4X". RSC Advances 10, nr 42 (2020): 24862–66. http://dx.doi.org/10.1039/d0ra05295g.
Pełny tekst źródłaSkalik, Joanna, Marek Koprowski, Ewa Różycka-Sokołowska i Piotr Bałczewski. "The hetero-Friedel-Crafts-Bradsher Cyclizations with Formation of Ring Carbon-Heteroatom (P, S) Bonds, Leading to Organic Functional Materials". Materials 13, nr 21 (23.10.2020): 4751. http://dx.doi.org/10.3390/ma13214751.
Pełny tekst źródłaJeong, Jaeryeol, i Min Hyung Lee. "Charge Transfer-Induced Geometric Distortion in Ni(HCO3)2@CNT: Impact on Enhanced Catalytic Performance for Oxygen Evolution and Reduction Reactions". ECS Meeting Abstracts MA2023-02, nr 58 (22.12.2023): 2790. http://dx.doi.org/10.1149/ma2023-02582790mtgabs.
Pełny tekst źródłaRai, Vijai K., Fooleswar Verma, Suhasini Mahata, Smita R. Bhardiya, Manorama Singh i Ankita Rai. "Metal Doped-C3N4/Fe2O4: Efficient and Versatile Heterogenous Catalysts for Organic Transformations". Current Organic Chemistry 23, nr 12 (20.09.2019): 1284–306. http://dx.doi.org/10.2174/1385272823666190709113758.
Pełny tekst źródłaRozprawy doktorskie na temat "Carbon-hetero bond"
Pariyar, Gyan Chandra. "Explorative studies on carbon hetero bond transformation reaction and carbon-hetero bond formation reaction". Thesis, University of North Bengal, 2018. http://ir.nbu.ac.in/handle/123456789/2813.
Pełny tekst źródłaMukherjee, Suvodip. "Methodological approach on carbon-hetero bond formation reaction". Thesis, University of North Bengal, 2022. http://ir.nbu.ac.in/handle/123456789/4792.
Pełny tekst źródłaJha, Satadru. "Organic reactions methodology : studies on carbon-nitrogen hetero bond forming reactions". Thesis, University of North Bengal, 2004. http://hdl.handle.net/123456789/745.
Pełny tekst źródłaSenecal, Todd D. (Todd Dale). "Carbon-trifluoromethyl bond forming reactions and palladium-catalyzed cyanation of (hetero)aryl halides". Thesis, Massachusetts Institute of Technology, 2013. http://hdl.handle.net/1721.1/82321.
Pełny tekst źródłaCataloged from PDF version of thesis.
Includes bibliographical references.
Chapter 1 Nucleophilic trifluoromethyl sources were systematically examined in stoichiometric palladium experiments to determine the most efficient class of reagents for transmetallation. In conjunction with reductive elimination studies, this led to the development of the first system for the trifluoromethylation of aryl chlorides. Chapter 2 A method for the oxidative trifluoromethylation of (hetero)aryl boronic acids is reported. Bench top setup and visual reaction monitoring makes this process particularly well suited to medicinal and academic chemists. Fast reaction times allow for the trifluoromethylation of heterocyclic boronic acids that are prone to facile protodeboronation. Chapter 3 A trifluoromethylation of potassium vinyl trifluoroborates via iron catalysis has been developed. Excellent E:Z ratios are observed for styryl trifluoroborates. Initial investigations suggest a mechanistic pathway that diverges from our previous (hetero)aryl trifluoromethylation systems. Chapter 4 A highly efficient system for the palladium-catalyzed cyanation of (hetero)aryl halides is disclosed. By employing palladacycle precatalysts, cyanide binding during catalyst formation is minimized, allowing for low catalyst loadings even with unactivated aryl chlorides. The method utilizes a non-toxic cyanide source and exhibits excellent functional group tolerance, particularly of free N-H groups and typically challenging five membered heterocycles.
by Todd D. Senecal.
Ph.D.in Organic Chemistry
Dong, Boliang. "Formation of Carbon-Carbon and Carbon-Hetero Bonds through Gold Catalysis". Scholar Commons, 2017. https://scholarcommons.usf.edu/etd/7396.
Pełny tekst źródłaRokade, Balaji Vasantrao. "Copper-Catalyzed Novel Oxidative Transformations : Construction of Carbon-Hetero Bonds". Thesis, 2014. http://etd.iisc.ac.in/handle/2005/3479.
Pełny tekst źródłaRokade, Balaji Vasantrao. "Copper-Catalyzed Novel Oxidative Transformations : Construction of Carbon-Hetero Bonds". Thesis, 2014. http://etd.iisc.ernet.in/2005/3479.
Pełny tekst źródłaGuan, Shih-Hau, i 管仕豪. "Studies of Carbon-Carbon Bond Formation Reactions Based on Ni(II) and Pd(II) Catalysts Bearing Nitrogen-Containing Hetero-functional Bidentate Ligands". Thesis, 2007. http://ndltd.ncl.edu.tw/handle/64240078354258185606.
Pełny tekst źródła國立臺灣大學
化學研究所
95
In this thesis, carbon-carbon bond formations are studied through three kinds of reactions: styrene polymerization, cross-couplings and nucleophilic additions. A new series of Ni(II) complexes [(N,N'')NiBr2] bearing bidentate amino-oxazoline ligands have been synthesized and applied for polymerization of styrene. With cocatalyst, MAO, these Ni(II) complexes 4 are highly efficient catalysts for styrene polymerization with activities up to ~107 g / mol [Ni] × h under optimized conditions, which possess the best performance among the catalytic Ni systems now. Effects of the structures of catalysts and the reaction parameters on the activities and characteristic properties for the polymers have been discussed here. From the 13C NMR data, the degree of stereoregularity of the synthesized polystyrene could be moderately controlled by the chiral center in the oxazoline ring although atactic polymers were generally obtained by these Ni(II) catalysts. The neutral Pd(II) complexes [(N,N'')PdCH3Cl] 5 and the cationic complexes [(N,N'')PdCH3L]+ 7 were prepared for studying the mechanism for polymerization. For the neutral Pd complexes, their coordination chemistry, dynamic behavior, geometric isomerization, and reactivity toward alkynes have been studied herein. Furthermore, reactions of cationic Pd complexes with styrene, which led to the η3-π-benzyl Pd(II) complexes, made the possible mechanism of the polymerization of styrene for the Ni(II) system. Neutral Pd(II) complexes were synthesized and involved nitrogen-containing ligands, such as mono-oxazolines, amino-oxazolines and pyridyl-pyrazoles. Among them, the chloromethylpalladium(II) complex with bidentate pyridyl-pyrazole ligands exhibited excellent activities toward Heck coupling reactions with high TONs up to 95,000,000, comparable to the palladacycle systems. In addition, the pyridyl-azolate ligands are good candidates for catalytic Suzuki-Miyaura cross-coupling reactions. In the presence of Pd(OAc)2, KF as base, and such ligands in EtOH, the couplings of aryl bromides with phenylboronic acids could proceed with high conversions at room temperature in the air. Under the same conditions, it could slowly couple aryl chloride with phenylboronic acids, which is rare for Pd catalysts with bidentate nitrogen donor ligands. Finally, we synthesized a series of cationic allylpalladium(II) complexes bearing asymmetric amino-oxazoline ligands. The isomer interconversion is demonstrated by NOESY spectra to show a syn-syn, anti-anti exchange. Nucleophilic attacks to the Pd complexes would result in the linear and branched products. The regioselectivity is strongly dependent on the steric/electronic properties of the nucleophiles and the polarity of the used solvents.
Guan, Shih-Hau. "Studies of Carbon-Carbon Bond Formation Reactions Based on Ni(II) and Pd(II) Catalysts Bearing Nitrogen-Containing Hetero-functional Bidentate Ligands". 2007. http://www.cetd.com.tw/ec/thesisdetail.aspx?etdun=U0001-1108200716185900.
Pełny tekst źródłaDhineshkumar, J. "Iodine and Copper Catalyzed Oxidative Cross Coupling Reactions : Design and Development of Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions". Thesis, 2016. http://etd.iisc.ac.in/handle/2005/3020.
Pełny tekst źródłaCzęści książek na temat "Carbon-hetero bond"
Zaman, Khurshid, Atta-Ur-Rahman i Saleh Shekhani. "Asymmetric Carbon-Hetero Bond Formations". W Yearbook of Asymmetric Synthesis 1991, 177–201. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-0235-3_4.
Pełny tekst źródłaGrosche, Philipp, Jörg Rademann i Günther Jung. "Addition to Carbon-Hetero Multiple Bonds". W Handbook of Combinatorial Chemistry, 322–45. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2004. http://dx.doi.org/10.1002/3527603034.ch12.
Pełny tekst źródła"7. Photoredox catalyzed α-functionalization of amines – visible light mediated carbon-carbon and carbon-hetero bond forming reactions". W Chemical Photocatalysis, 147–62. De Gruyter, 2020. http://dx.doi.org/10.1515/9783110576764-007.
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