Bibliografías temáticas / Oxidative arylation / Artículos de revistas

Artículos de revistas sobre el tema "Oxidative arylation"

Siga este enlace para ver otros tipos de publicaciones sobre el tema: Oxidative arylation.
Autor: Grafiati
Publicado: 7 de julio de 2024
Última modificación: 7 de julio de 2024

Crea una cita precisa en los estilos APA, MLA, Chicago, Harvard y otros

Elija tipo de fuente:

Consulte los 50 mejores artículos de revistas para su investigación sobre el tema "Oxidative arylation".

Junto a cada fuente en la lista de referencias hay un botón "Agregar a la bibliografía". Pulsa este botón, y generaremos automáticamente la referencia bibliográfica para la obra elegida en el estilo de cita que necesites: APA, MLA, Harvard, Vancouver, Chicago, etc.

También puede descargar el texto completo de la publicación académica en formato pdf y leer en línea su resumen siempre que esté disponible en los metadatos.

Explore artículos de revistas sobre una amplia variedad de disciplinas y organice su bibliografía correctamente.

1

Zhou, Yao, Ya Wang, Zhiyi Song, Tamaki Nakano y Qiuling Song. "Cu-catalyzed C–N bond cleavage of 3-aminoindazoles for the C–H arylation of enamines". Organic Chemistry Frontiers 7, n.º 1 (2020): 25–29. http://dx.doi.org/10.1039/c9qo01177c.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
2

Wei, Xiao-Hong, Gang-Wei Wang y Shang-Dong Yang. "Enantioselective synthesis of arylglycine derivatives by direct C–H oxidative cross-coupling". Chemical Communications 51, n.º 5 (2015): 832–35. http://dx.doi.org/10.1039/c4cc07361d.

Texto completo
Resumen
A new method for the synthesis of chiral α-amino acid derivatives by enantioselective C–H arylation of N-aryl glycine esters with aryl boric acids by direct C–H oxidative cross-coupling has been performed. This work successfully integrates the direct C–H oxidation with asymmetric arylation and exhibits excellent enantioselectivity.
Los estilos APA, Harvard, Vancouver, ISO, etc.
3

Park, Soo J., Jason R. Price y Matthew H. Todd. "Oxidative Arylation of Isochroman". Journal of Organic Chemistry 77, n.º 2 (29 de diciembre de 2011): 949–55. http://dx.doi.org/10.1021/jo2021373.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
4

Yu, Congjun y Frederic W. Patureau. "Regioselective Oxidative Arylation of Fluorophenols". Angewandte Chemie International Edition 58, n.º 51 (31 de octubre de 2019): 18530–34. http://dx.doi.org/10.1002/anie.201910352.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
5

Singh, Keisham. "Recent Advances in C–H Bond Functionalization with Ruthenium-Based Catalysts". Catalysts 9, n.º 2 (12 de febrero de 2019): 173. http://dx.doi.org/10.3390/catal9020173.

Texto completo
Resumen
The past decades have witnessed rapid development in organic synthesis via catalysis, particularly the reactions through C–H bond functionalization. Transition metals such as Pd, Rh and Ru constitute a crucial catalyst in these C–H bond functionalization reactions. This process is highly attractive not only because it saves reaction time and reduces waste,but also, more importantly, it allows the reaction to be performed in a highly region specific manner. Indeed, several organic compounds could be readily accessed via C–H bond functionalization with transition metals. In the recent past, tremendous progress has been made on C–H bond functionalization via ruthenium catalysis, including less expensive but more stable ruthenium(II) catalysts. The ruthenium-catalysed C–H bond functionalization, viz. arylation, alkenylation, annulation, oxygenation, and halogenation involving C–C, C–O, C–N, and C–X bond forming reactions, has been described and presented in numerous reviews. This review discusses the recent development of C–H bond functionalization with various ruthenium-based catalysts. The first section of the review presents arylation reactions covering arylation directed by N–Heteroaryl groups, oxidative arylation, dehydrative arylation and arylation involving decarboxylative and sp3-C–H bond functionalization. Subsequently, the ruthenium-catalysed alkenylation, alkylation, allylation including oxidative alkenylation and meta-selective C–H bond alkylation has been presented. Finally, the oxidative annulation of various arenes with alkynes involving C–H/O–H or C–H/N–H bond cleavage reactions has been discussed.
Los estilos APA, Harvard, Vancouver, ISO, etc.
6

Hata, Kazuhiro, Hideto Ito, Yasutomo Segawa y Kenichiro Itami. "Pyridylidene ligand facilitates gold-catalyzed oxidative C–H arylation of heterocycles". Beilstein Journal of Organic Chemistry 11 (28 de diciembre de 2015): 2737–46. http://dx.doi.org/10.3762/bjoc.11.295.

Texto completo
Resumen
Triaryl-2-pyridylidene effectively facilitates the gold-catalyzed oxidative C–H arylation of heteroarenes with arylsilanes as a unique electron-donating ligand on gold. The employment of the 2-pyridylidene ligand, which is one of the strongest electron-donating N-heterocyclic carbenes, resulted in the rate acceleration of the C–H arylation reaction of heterocycles over conventional ligands such as triphenylphosphine and a classical N-heterocyclic carbene. In situ observation and isolation of the 2-pyridylidene-gold(III) species, as well as a DFT study, indicated unusual stability of gold(III) species stabilized by strong electron donation from the 2-pyridylidene ligand. Thus, the gold(I)-to-gold(III) oxidation process is thought to be facilitated by the highly electron-donating 2-pyridylidene ligand.
Los estilos APA, Harvard, Vancouver, ISO, etc.
7

Chen, Wei W., Nahiane Pipaon Fernández, Marta Díaz Baranda, Anton Cunillera, Laura G. Rodríguez, Alexandr Shafir y Ana B. Cuenca. "Exploring benzylic gem-C(sp3)–boron–silicon and boron–tin centers as a synthetic platform". Chemical Science 12, n.º 31 (2021): 10514–21. http://dx.doi.org/10.1039/d1sc01741a.

Texto completo
Resumen
This work explores divergent reactivity of the benzylic gem-boron–silicon and boron–tin double nucleophiles, including the arylation of the C–B bond with Ar–Cl, along with a complementary oxidative λ3-iodane-guided arylation of the C–Si/Sn moiety.
Los estilos APA, Harvard, Vancouver, ISO, etc.
8

Ho, Nga Kim T., Beate Neumann, Hans-Georg Stammler, Vitor H. Menezes da Silva, Daniel G. Watanabe, Ataualpa A. C. Braga y Rajendra S. Ghadwal. "Nickel-catalysed direct C2-arylation of N-heterocyclic carbenes". Dalton Transactions 46, n.º 36 (2017): 12027–31. http://dx.doi.org/10.1039/c7dt03099a.

Texto completo
Resumen
Direct C2-arylation of NHCs to C2-arylated imidazolium salts (III) is achieved using Ni-catalysis. The dinuclear Ni(i) species I undergoes oxidative addition with ArX to give the Ni(ii) intermediate II. Reductive elimination delivers the arylation product III and regenerates the catalyst I.
Los estilos APA, Harvard, Vancouver, ISO, etc.
9

Chen, Kai, Xin Li, Shuo-Qing Zhang y Bing-Feng Shi. "Palladium-catalyzed C(sp3)–H arylation of lactic acid: efficient synthesis of chiral β-aryl-α-hydroxy acids". Organic Chemistry Frontiers 3, n.º 2 (2016): 204–8. http://dx.doi.org/10.1039/c5qo00319a.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
10

Querard, Pierre, Inna Perepichka, Eli Zysman-Colman y Chao-Jun Li. "Copper-catalyzed asymmetric sp3 C–H arylation of tetrahydroisoquinoline mediated by a visible light photoredox catalyst". Beilstein Journal of Organic Chemistry 12 (6 de diciembre de 2016): 2636–43. http://dx.doi.org/10.3762/bjoc.12.260.

Texto completo
Resumen
This report describes a highly enantioselective oxidative sp3 C–H arylation of N-aryltetrahydroisoquinolines (THIQs) through a dual catalysis platform. The combination of the photoredox catalyst, [Ir(ppy)2(dtbbpy)]PF6, and chiral copper catalysts provide a mild and highly effective sp3 C–H asymmetric arylation of THIQs.
Los estilos APA, Harvard, Vancouver, ISO, etc.
11

Yuan, Jin-Wei, Wei-Jie Li, Liang-Ru Yang, Pu Mao y Yong-Mei Xiao. "Regioselective C-3 arylation of coumarins with arylhydrazines via radical oxidation by potassium permanganate". Zeitschrift für Naturforschung B 71, n.º 11 (1 de noviembre de 2016): 1115–23. http://dx.doi.org/10.1515/znb-2016-0109.

Texto completo
Resumen
AbstractAn efficient protocol for oxidative C-3 arylation of coumarins with arylhydrazine has been developed using potassium permanganate as an oxidant. The arylated coumarins with different electronic properties were obtained in moderate to good yields. The developed protocol for direct C-3 arylation of coumarins could be extended to quinolinones.
Los estilos APA, Harvard, Vancouver, ISO, etc.
12

Park, Soo J., Jason R. Price y Matthew H. Todd. "ChemInform Abstract: Oxidative Arylation of Isochroman." ChemInform 43, n.º 21 (26 de abril de 2012): no. http://dx.doi.org/10.1002/chin.201221135.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
13

Faradhiyani, Alanna, Qiao Zhang, Keisuke Maruyama, Junpei Kuwabara, Takeshi Yasuda y Takaki Kanbara. "Synthesis of bithiazole-based semiconducting polymers via Cu-catalysed aerobic oxidative coupling". Materials Chemistry Frontiers 2, n.º 7 (2018): 1306–9. http://dx.doi.org/10.1039/c7qm00584a.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
14

Bu, Meijie, Teng Fei Niu y Chun Cai. "Visible-light-mediated oxidative arylation of vinylarenes under aerobic conditions". Catalysis Science & Technology 5, n.º 2 (2015): 830–34. http://dx.doi.org/10.1039/c4cy01523a.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
15

Shen, Xianfu, Yongyun Zhou, Yongkai Xi, Jingfeng Zhao y Hongbin Zhang. "Copper catalyzed sequential arylation−oxidative dimerization of o-haloanilides: synthesis of dimeric HPI alkaloids". Chemical Communications 51, n.º 80 (2015): 14873–76. http://dx.doi.org/10.1039/c5cc05378a.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
16

Jiang, Huanfeng, Wanfei Yang, Huoji Chen, Jianxiao Li y Wanqing Wu. "Palladium-catalyzed aerobic oxidative allylic C–H arylation of alkenes with polyfluorobenzenes". Chem. Commun. 50, n.º 54 (2014): 7202–4. http://dx.doi.org/10.1039/c4cc02023e.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
17

Ghosh, Asim Kumar, Sadhanendu Samanta, Payel Ghosh, Sukanya Neogi y Alakananda Hajra. "Regioselective hydroarylation and arylation of maleimides with indazoles via a Rh(iii)-catalyzed C–H activation". Organic & Biomolecular Chemistry 18, n.º 16 (2020): 3093–97. http://dx.doi.org/10.1039/d0ob00353k.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
18

Chen, Lijun, Lin Ju, Katelyn A. Bustin y Jessica M. Hoover. "Copper-catalyzed oxidative decarboxylative C–H arylation of benzoxazoles with 2-nitrobenzoic acids". Chemical Communications 51, n.º 81 (2015): 15059–62. http://dx.doi.org/10.1039/c5cc06645j.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
19

GUO, HAN y YING XUE. "THEORETICAL STUDY ON CUI-CATALYZED LIGAND-FREE N-ARYLATION OF IMIDAZOLE WITH BROMOBENZENE". Journal of Theoretical and Computational Chemistry 11, n.º 05 (octubre de 2012): 1135–47. http://dx.doi.org/10.1142/s0219633612500757.

Texto completo
Resumen
The density functional theory (DFT) is used to investigate the mechanism of ligand-free CuI -catalyzed N -arylation of imidazole with aryl halide. The oxidative addition/reductive elimination mechanism is adopted via two different pathways to form the same Cu(III) intermediate. Comparing two pathways, the path 1 in which the imidazolyl coordination occurs prior to the oxidative addition is more favorable, because the free energy barrier of the rate-limiting step of path 1 is lower than the barrier of the other. In addition, it leads to a relative stable intermediate which can promote the reaction to process via path 1. And the overall free energy barrier of oxidative addition to imidazole-ligated Cu(I) complex is not high enough when comparing with the diamine-promote process, which can further prove that the N -arylation of imidazole is feasible in the absence of additional ligands. Nucleophile coordination and reductive elimination steps are facile, while the oxidative addition is the rate-limiting step.
Los estilos APA, Harvard, Vancouver, ISO, etc.
20

Jiang, Tuo, Andreas K. Å. Persson y Jan-E. Bäckvall. "Palladium-Catalyzed Oxidative Carbocyclization/Arylation of Enallenes". Organic Letters 13, n.º 21 (4 de noviembre de 2011): 5838–41. http://dx.doi.org/10.1021/ol202451f.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
21

Lee, Kathleen S. y Joseph M. Ready. "Titanium-Mediated Oxidative Arylation of Homoallylic Alcohols". Angewandte Chemie International Edition 50, n.º 9 (25 de enero de 2011): 2111–14. http://dx.doi.org/10.1002/anie.201007244.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
22

Lee, Kathleen S. y Joseph M. Ready. "Titanium-Mediated Oxidative Arylation of Homoallylic Alcohols". Angewandte Chemie 123, n.º 9 (25 de enero de 2011): 2159–62. http://dx.doi.org/10.1002/ange.201007244.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
23

Huang, Guanghao, Lin Lu, Huanfeng Jiang y Biaolin Yin. "Aerobic oxidative α-arylation of furans with boronic acids via Pd(ii)-catalyzed C–C bond cleavage of primary furfuryl alcohols: sustainable access to arylfurans". Chemical Communications 53, n.º 90 (2017): 12217–20. http://dx.doi.org/10.1039/c7cc07111f.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
24

Fan, Jian, Li Li, Jitan Zhang y Meihua Xie. "Expeditious synthesis of phenanthridines through a Pd/MnO2-mediated C–H arylation/oxidative annulation cascade from aldehydes, aryl iodides and amino acids". Chemical Communications 56, n.º 18 (2020): 2775–78. http://dx.doi.org/10.1039/d0cc00300j.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
25

Luo, Haiqing, Qi Xie, Kai Sun, Jianbo Deng, Lin Xu, Kejun Wang y Xuzhong Luo. "Rh(iii)-catalyzed C-7 arylation of indolines with arylsilanes via C–H activation". RSC Advances 9, n.º 32 (2019): 18191–95. http://dx.doi.org/10.1039/c9ra04142g.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
26

Araneo, Silvia, Francesca Fontana, Francesco Minisci, Francesco Recupero y Anna Serri. "Hydroperoxides as pseudohalides: oxidation, oxidative alkylation, acylation and arylation of acrylonitrile". Journal of the Chemical Society, Chemical Communications, n.º 14 (1995): 1399. http://dx.doi.org/10.1039/c39950001399.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
27

Chen, Xin, Yunyun Bian, Baichuan Mo, Peng Sun, Chunxia Chen y Jinsong Peng. "Copper(ii)-catalyzed synthesis of multisubstituted indoles through sequential Chan–Lam and cross-dehydrogenative coupling reactions". RSC Advances 10, n.º 42 (2020): 24830–39. http://dx.doi.org/10.1039/d0ra04592f.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
28

Yuan, Jin-Wei, Liang-Ru Yang, Pu Mao y Ling-Bo Qu. "AgNO3-catalyzed direct C–H arylation of quinolines by oxidative decarboxylation of aromatic carboxylic acids". Organic Chemistry Frontiers 4, n.º 4 (2017): 545–54. http://dx.doi.org/10.1039/c6qo00533k.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
29

Morimoto, Koji, Yusuke Ohnishi, Daichi Koseki, Akira Nakamura, Toshifumi Dohi y Yasuyuki Kita. "Stabilized pyrrolyl iodonium salts and metal-free oxidative cross-coupling". Organic & Biomolecular Chemistry 14, n.º 38 (2016): 8947–51. http://dx.doi.org/10.1039/c6ob01764a.

Texto completo
Resumen
We have developed a direct oxidative C–H bond arylation of pyrroles with various aromatic compounds via stabilized pyrrolyl iodonium(iii) salts generated from modified hypervalent iodine(iii) and TMSCl as an activator.
Los estilos APA, Harvard, Vancouver, ISO, etc.
30

Terai, Seiya, Yuki Sato, Takuya Kochi y Fumitoshi Kakiuchi. "Efficient synthesis of 3,6,13,16-tetrasubstituted-tetrabenzo[a,d,j,m]coronenes by selective C–H/C–O arylations of anthraquinone derivatives". Beilstein Journal of Organic Chemistry 16 (31 de marzo de 2020): 544–50. http://dx.doi.org/10.3762/bjoc.16.51.

Texto completo
Resumen
An efficient synthesis of tetrabenzo[a,d,j,m]coronene derivatives having alkyl and alkoxy substituents at the 3, 6, 13, and 16-positions was achieved based on the ruthenium-catalyzed coupling reactions of anthraquinone derivatives with arylboronates via C–H and C–O bond cleavage. The reaction sequence involving the arylation, carbonyl methylenation, and oxidative cyclization effectively provided various tetrabenzo[a,d,j,m]coronenes in short steps from readily available starting materials. Tetrabenzo[a,d,j,m]coronenes possessing two different types of substituents were obtained selectively by sequential chemoselective C–O arylation and C–H arylation. The 1H NMR spectra of the tetrabenzo[a,d,j,m]coronene product indicated its self-assembling behavior in CDCl3.
Los estilos APA, Harvard, Vancouver, ISO, etc.
31

Nareddy, Pradeep, Frank Jordan y Michal Szostak. "Ruthenium(ii)-catalyzed ortho-C–H arylation of diverse N-heterocycles with aryl silanes by exploiting solvent-controlled N-coordination". Organic & Biomolecular Chemistry 15, n.º 22 (2017): 4783–88. http://dx.doi.org/10.1039/c7ob00818j.

Texto completo
Resumen
We report the first method for the direct, regioselective Ru(ii)-catalyzed oxidative arylation of C–H bonds in diverse N-heterocycles with aryl silanes by exploiting solvent-controlled N-coordination.
Los estilos APA, Harvard, Vancouver, ISO, etc.
32

Laha, Joydev K., Shubhra Sharma, Rohan A. Bhimpuria, Neetu Dayal, Gurudutt Dubey y Prasad V. Bharatam. "Integration of oxidative arylation with sulfonyl migration: one-pot tandem synthesis of densely functionalized (NH)-pyrroles". New Journal of Chemistry 41, n.º 17 (2017): 8791–803. http://dx.doi.org/10.1039/c7nj01709j.

Texto completo
Resumen
A one-pot synthesis of 2-aryl-3-alkyl/aryl-sulfonyl-(NH)-pyrroles from N-sulfonylpyrroles, developed for the first time, via palladium-catalyzed oxidative C-2 arylation followed by sulfonyl migration is described.
Los estilos APA, Harvard, Vancouver, ISO, etc.
33

Rodriguez, Jessica, Abdallah Zeineddine, E. Daiann Sosa Carrizo, Karinne Miqueu, Nathalie Saffon-Merceron, Abderrahmane Amgoune y Didier Bourissou. "Catalytic Au(i)/Au(iii) arylation with the hemilabile MeDalphos ligand: unusual selectivity for electron-rich iodoarenes and efficient application to indoles". Chemical Science 10, n.º 30 (2019): 7183–92. http://dx.doi.org/10.1039/c9sc01954e.

Texto completo
Resumen
The ability of the MeDalphos ligand to trigger oxidative addition of iodoarenes preferentially electron-rich, to gold has been thoroughly studied and exploited to develop an efficient Au(i)/Au(iii)-catalysed C3-arylation of indoles.
Los estilos APA, Harvard, Vancouver, ISO, etc.
34

Zhang, Shuyao, Xiaohan Ye, Lukasz Wojtas, Wenyan Hao y Xiaodong Shi. "Electrochemical gold redox catalysis for selective oxidative arylation". Green Synthesis and Catalysis 2, n.º 1 (febrero de 2021): 82–86. http://dx.doi.org/10.1016/j.gresc.2021.01.008.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
35

Volla, Chandra M. R. y Jan-E. Bäckvall. "Palladium-Catalyzed Oxidative Domino Carbocyclization–Arylation of Bisallenes". ACS Catalysis 6, n.º 10 (29 de agosto de 2016): 6398–402. http://dx.doi.org/10.1021/acscatal.6b02070.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
36

Basnet, Prakash, Melissa B. Sebold, Charles E. Hendrick y Marisa C. Kozlowski. "Copper Catalyzed Oxidative Arylation of Tertiary Carbon Centers". Organic Letters 22, n.º 24 (2 de diciembre de 2020): 9524–28. http://dx.doi.org/10.1021/acs.orglett.0c03581.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
37

Wolf, C. y R. Lerebours. "Arylation and Oxidative Esterification of Aldehydes with Siloxanes". Synfacts 2006, n.º 12 (diciembre de 2006): 1277. http://dx.doi.org/10.1055/s-2006-955616.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
38

Bagnell, Laurence, Ulf Kreher y Christopher R. Strauss. "Pd-catalysed arylation of propan-1-ol and derivatives: oxidative role of the arylating agent". Chemical Communications, n.º 1 (2001): 29–30. http://dx.doi.org/10.1039/b005323f.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
39

Matsumoto, Takaya y Hajime Yoshida. "Oxidative Arylation of Ethylene with Benzene to Produce Styrene". Chemistry Letters 29, n.º 9 (septiembre de 2000): 1064–65. http://dx.doi.org/10.1246/cl.2000.1064.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
40

Vershinin, Vlada, Alina Dyadyuk y Doron Pappo. "Iron-catalyzed selective oxidative arylation of phenols and biphenols". Tetrahedron 73, n.º 26 (junio de 2017): 3660–68. http://dx.doi.org/10.1016/j.tet.2017.03.094.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
41

Kapłon, Katarzyna, Oleg M. Demchuk, Marta Wieczorek y K. Michał Pietrusiewicz. "Brönsted acid catalyzed direct oxidative arylation of 1,4-naphthoquinone". Current Chemistry Letters 3, n.º 1 (2013): 23–36. http://dx.doi.org/10.5267/j.ccl.2013.10.001.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
42

Cai, Chun, Jie Feng, Guoping Lu y Meifang Lv. "Palladium(II)-Catalyzed Oxidative ortho-Arylation of 2-Phenylpyridines". Synlett 24, n.º 16 (21 de agosto de 2013): 2153–59. http://dx.doi.org/10.1055/s-0033-1339516.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
43

Hofer, Manuel, Alexandre Genoux, Roopender Kumar y Cristina Nevado. "Gold-Catalyzed Direct Oxidative Arylation with Boron Coupling Partners". Angewandte Chemie International Edition 56, n.º 4 (21 de diciembre de 2016): 1021–25. http://dx.doi.org/10.1002/anie.201610457.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
44

Hofer, Manuel, Alexandre Genoux, Roopender Kumar y Cristina Nevado. "Gold-Catalyzed Direct Oxidative Arylation with Boron Coupling Partners". Angewandte Chemie 129, n.º 4 (21 de diciembre de 2016): 1041–45. http://dx.doi.org/10.1002/ange.201610457.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
45

Lee, Kathleen S. y Joseph M. Ready. "ChemInform Abstract: Titanium-Mediated Oxidative Arylation of Homoallylic Alcohols." ChemInform 42, n.º 24 (19 de mayo de 2011): no. http://dx.doi.org/10.1002/chin.201124090.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
46

Zhang, Rui, Qin Xu, Kai Chen, Peng Gu y Min Shi. "Gold-Catalyzed Cascade Oxidative Cyclization and Arylation of Allenoates". European Journal of Organic Chemistry 2013, n.º 32 (24 de septiembre de 2013): 7366–71. http://dx.doi.org/10.1002/ejoc.201300896.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
47

Jiang, Tuo, Andreas K. Aa Persson y Jan-E. Baeckvall. "ChemInform Abstract: Palladium-Catalyzed Oxidative Carbocyclization/Arylation of Enallenes." ChemInform 43, n.º 12 (23 de febrero de 2012): no. http://dx.doi.org/10.1002/chin.201212049.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
48

ARANEO, S., F. FONTANA, F. MINISCI, F. RECUPERO y A. SERRI. "ChemInform Abstract: Hydroperoxides as Pseudohalides: Oxidation, Oxidative Alkylation, Acylation and Arylation of Acrylonitrile." ChemInform 26, n.º 48 (17 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199548077.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
49

Maurya, Sundaram, Sandip B. Jadhav y Rambabu Chegondi. "Metal-free oxidative formal C(sp2)–H arylation of cyclopentene-1,3-diones with β-naphthols". Organic & Biomolecular Chemistry 20, n.º 10 (2022): 2059–63. http://dx.doi.org/10.1039/d2ob00156j.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
50

Hong, Fenglin, Nannan Lu, Beili Lu y Jiajia Cheng. "Synthesis of Fused Heterocycles via One-pot Oxidative O-Arylation, Pd-Catalyzed C(sp3)-H Arylation". Advanced Synthesis & Catalysis 359, n.º 19 (21 de agosto de 2017): 3299–303. http://dx.doi.org/10.1002/adsc.201700761.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
Ofrecemos descuentos en todos los planes premium para autores cuyas obras están incluidas en selecciones literarias temáticas. ¡Contáctenos para obtener un código promocional único!

Pasar a la bibliografía