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Artículos de revistas sobre el tema "Coupling Benzynes"

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Publicado: 6 de septiembre de 2023

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1

Ikawa, Takashi, Hideki Kaneko, Shigeaki Masuda, Erika Ishitsubo, Hiroaki Tokiwa y Shuji Akai. "Trifluoromethanesulfonyloxy-group-directed regioselective (3 + 2) cycloadditions of benzynes for the synthesis of functionalized benzo-fused heterocycles". Organic & Biomolecular Chemistry 13, n.º 2 (2015): 520–26. http://dx.doi.org/10.1039/c4ob01627k.

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2

Bao, Zhicheng, Chaoqiang Wu y Jianbo Wang. "Palladium-Catalyzed Three-Component Coupling of Benzynes, Benzylic/Allylic Bromides and 1,1-Bis[(pinacolato)boryl]methane". Catalysts 13, n.º 1 (5 de enero de 2023): 126. http://dx.doi.org/10.3390/catal13010126.

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We report herein a palladium-catalyzed three-component cross-coupling reaction of 2-(trimethylsilyl)phenyl trifluoromethanesulfonate, benzylic/allylic bromides and 1,1-bis[(pinacolato)boryl]methane. The reaction, which affords benzyl boronates as the products, represents the first example of using 1,1-bis[(pinacolato)boryl]methane in a cross-coupling reaction involving benzyne species.
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3

Lu, Tianhao, Yong Shen, Min Wang, Zibing Zhang, Shijun Li y Chunsong Xie. "Aerobic Cu-catalyzed oxidative 1 : 2 coupling of benzynes with terminal alkynes". Chemical Communications 56, n.º 59 (2020): 8214–17. http://dx.doi.org/10.1039/d0cc03150j.

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4

Lee, Yi-Hsien, Yen-Chung Chen y Jen-Chieh Hsieh. "Pyridine-Catalyzed Double C-N Coupling Reaction of an Isocyanate with Two Benzynes". European Journal of Organic Chemistry 2012, n.º 2 (21 de noviembre de 2011): 247–50. http://dx.doi.org/10.1002/ejoc.201101251.

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5

Lee, Yi-Hsien, Yen-Chung Chen y Jen-Chieh Hsieh. "ChemInform Abstract: Pyridine-Catalyzed Double C-N Coupling Reaction of an Isocyanate with Two Benzynes." ChemInform 43, n.º 22 (3 de mayo de 2012): no. http://dx.doi.org/10.1002/chin.201222064.

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6

Yang, Yun-Yun, Wang-Ge Shou y Yan-Guang Wang. "Tandem coupling reactions of benzynes and 1,3-diones: a novel synthesis of 2,2-diphenyl-1,3-diones". Tetrahedron Letters 48, n.º 46 (noviembre de 2007): 8163–65. http://dx.doi.org/10.1016/j.tetlet.2007.09.092.

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7

Jeganmohan, Masilamani, Sivakolundu Bhuvaneswari y Chien-Hong Cheng. "A Cooperative Copper- and Palladium-Catalyzed Three-Component Coupling of Benzynes, Allylic Epoxides, and Terminal Alkynes". Angewandte Chemie International Edition 48, n.º 2 (2 de enero de 2009): 391–94. http://dx.doi.org/10.1002/anie.200804873.

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8

Jeganmohan, Masilamani, Sivakolundu Bhuvaneswari y Chien-Hong Cheng. "A Cooperative Copper- and Palladium-Catalyzed Three-Component Coupling of Benzynes, Allylic Epoxides, and Terminal Alkynes". Angewandte Chemie 121, n.º 2 (2 de enero de 2009): 397–400. http://dx.doi.org/10.1002/ange.200804873.

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9

Jayanth, Thiruvellore Thatai, Masilamani Jeganmohan y Chien-Hong Cheng. "Highly Efficient Route too-Allylbiaryls via Palladium-Catalyzed Three-Component Coupling of Benzynes, Allylic Halides, and Aryl Organometallic Reagents". Organic Letters 7, n.º 14 (julio de 2005): 2921–24. http://dx.doi.org/10.1021/ol050859r.

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10

Das, Eshani y Amit Basak. "Regioselective Synthesis of Benzo-Fused Tetrahydroisoquinoline-Based Biaryls through a Tandem One-Pot Halogenation of p-Benzynes from Enediynes and Suzuki-Miyaura Coupling". Journal of Organic Chemistry 85, n.º 4 (27 de diciembre de 2019): 2697–703. http://dx.doi.org/10.1021/acs.joc.9b02874.

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11

Buchwald, Stephen L., Brett T. Watson, Robert T. Lum y William A. Nugent. "A general method for the preparation of zirconocene complexes of substituted benzynes: in situ generation, coupling reactions, and use in the synthesis of polyfunctionalized aromatic compounds". Journal of the American Chemical Society 109, n.º 23 (noviembre de 1987): 7137–41. http://dx.doi.org/10.1021/ja00257a038.

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12

García-López, José-Antonio y Michael F. Greaney. "Synthesis of biaryls using aryne intermediates". Chemical Society Reviews 45, n.º 24 (2016): 6766–98. http://dx.doi.org/10.1039/c6cs00220j.

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13

Welsh, Erin N., Katherine N. Robertson y Alexander W. H. Speed. "Short syntheses of 1-substituted dibenzothiophene derivatives". Organic & Biomolecular Chemistry 19, n.º 9 (2021): 2000–2007. http://dx.doi.org/10.1039/d0ob01839b.

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14

Xia, Wujiong, Xinxin Zhao, Ming Chen, Binbin Huang, Chao Yang y Yuan Gao. "Photoinduced Cross-Coupling of Amines with 1,2-Diiodobenzene and Its Application in the Synthesis of Carbazoles". Synthesis 50, n.º 15 (8 de mayo de 2018): 2981–89. http://dx.doi.org/10.1055/s-0037-1609444.

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A facile and efficient process for the preparation of various tertiary aminobenzenes and carbazole derivatives via photoinduced cross-coupling of amines with 1,2-diiodobenzene is reported. Mechanistic investigations indicate that the transformation proceeds via nucleo­philic addition of an amine to the benzyne intermediate accompanied with a proton transfer process, followed by an oxidative cyclization of the generated diphenylamine to furnish the corresponding carbazole products.
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15

Henderson, Jaclyn L., Andrew S. Edwards y Michael F. Greaney. "Three-Component Coupling of Benzyne: Domino Intermolecular Carbopalladation". Journal of the American Chemical Society 128, n.º 23 (junio de 2006): 7426–27. http://dx.doi.org/10.1021/ja0615526.

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16

Bennett, Martin A. "Aryne Complexes of Zerovalent Metals of the Nickel Triad". Australian Journal of Chemistry 63, n.º 7 (2010): 1066. http://dx.doi.org/10.1071/ch10198.

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The chemistry of dihapto-aryne complexes of the zerovalent Group 10 metals of general formula [M(η2-aryne)L2] (M = Ni, Pd, Pt; L = various tertiary phosphines) is reviewed, with emphasis on the highly reactive nickel(0) compounds (aryne = benzyne, C6H4; 4,5-difluorobenzyne, 4,5-C6H2F2; 2,3-naphthalyne, 2,3-C10H6; L2 = 2 PEt3, 2 PiPr3, 2 PCy3, dcpe). These can be generated by alkali metal reduction of the appropriate (2-halogenoaryl)nickel(ii) halide precursors, such as [NiX(2-XC6H4)L2], which in turn are accessible by oxidative addition of the 1,2-dihaloarene to nickel(0) precursors such as [Ni(1,5-COD)2]. The X-ray structure of [Ni(η2-C6H4)(dcpe)] shows that this compound is a typical 16-electron Ni(0) (3d10) species in which benzyne acts as a 2π-electron donor. Several unusual organonickel compounds derived from [Ni(η2-4,5-C6H2F2)(PEt3)2] have been isolated recently, including [Ni2(μ-η2:η2-4,5-C6H2F2)(PEt3)4], in which a 4π-electron donor 4,5-difluorobenzyne is located at right-angles to a pair of nickel atoms. Free benzyne can be intercepted by both [Ni(η2-C2H4)(dcpe)] and [Pt(η2-C2H4)(PPh3)2], but the resulting benzyne complexes rapidly insert benzyne to give the appropriate η1:η1-2,2′-biphenylyl complexes. [Pt(η2-C6H4)(PPh3)2] also undergoes rapid ortho-metallation to give [PtPh(2-C6H4PPh2)(PPh3)]. However, a trapping reaction has been used to make the first 1,4-benzdiyne complex, [{Ni(dcpe)2}2(μ-η2:η2-1,4-C6H2)] by treatment of the 4-fluorobenzyne complex [Ni(η2-4-FC6H3)(dcpe)] with LiTMP. The use of alkali metals in the preparation of the η2-benzyne complexes is avoided in a more recently developed procedure, which starts from (2-bromophenyl)boronic acid, and is based on Suzuki–Miyaura coupling. This procedure has made accessible for the first time an aryne complex of palladium(0), [Pd(η2-C6H4)(PCy3)2], and the labile nickel(0) complex [Ni(η2-C6H4)(PPh3)2]. The aryne-nickel(0) complexes Ni(η2-aryne)L2 (L2 = 2 PEt3, dcpe) undergo sequential insertions into the aryne-metal bond with unsaturated molecules, such as CO, C2F4, substituted alkynes, substituted diynes, alkynylphosphines, and alkynyl thioethers, often with considerable regioselectivity. After the reductive elimination of two nickel-carbon σ-bonds, a variety of interesting polycyclic compounds can be obtained.
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17

McGlinchey, Michael J. y Kirill Nikitin. "Palladium-Catalysed Coupling Reactions En Route to Molecular Machines: Sterically Hindered Indenyl and Ferrocenyl Anthracenes and Triptycenes, and Biindenyls". Molecules 25, n.º 8 (22 de abril de 2020): 1950. http://dx.doi.org/10.3390/molecules25081950.

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Pd-catalysed Stille and Suzuki cross-couplings were used to prepare 9-(3-indenyl)-, 6, and 9-(2-indenyl)-anthracene, 7; addition of benzyne led to the 9-Indenyl-triptycenes, 8 and 9. In 6, [4 + 2] addition also occurred to the indenyl substituent. Reaction of 6 through 9 with Cr(CO)6 or Re2(CO)10 gave their M(CO)3 derivatives, where the Cr or Re was complexed to a six- or five-membered ring, respectively. In the 9-(2-indenyl)triptycene complexes, slowed rotation of the paddlewheel on the NMR time-scale was apparent in the η5-Re(CO)3 case and, when the η6-Cr(CO)3 was deprotonated, the resulting haptotropic shift of the metal tripod onto the five-membered ring also blocked paddlewheel rotation, thus functioning as an organometallic molecular brake. Suzuki coupling of ferrocenylboronic acid to mono- or dibromoanthracene yielded the ferrocenyl anthracenes en route to the corresponding triptycenes in which stepwise hindered rotations of the ferrocenyl groups behaved like molecular dials. CuCl2-mediated coupling of methyl- and phenyl-indenes yielded their rac and meso 2,2′-biindenyls; surprisingly, however, the apparently sterically crowded rac 2,2′-Bis(9-triptycyl)biindenyl functioned as a freely rotating set of molecular gears. The predicted high rotation barrier in 9-phenylanthracene was experimentally validated via the Pd-catalysed syntheses of di(3-fluorophenyl)anthracene and 9-(1-naphthyl)-10-phenylanthracene.
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18

Jones, Elizabeth P., Peter Jones, Andrew J. P. White y Anthony G. M. Barrett. "Asymmetric synthesis of quaternary aryl amino acid derivatives via a three-component aryne coupling reaction". Beilstein Journal of Organic Chemistry 7 (25 de noviembre de 2011): 1570–76. http://dx.doi.org/10.3762/bjoc.7.185.

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A method was developed for the synthesis of α-alkyl, α-aryl-bislactim ethers in good to excellent yields and high diastereoselectivities, consisting of a facile one-pot procedure in which the aryl group is introduced by means of a nucleophilic addition to benzyne and the alkyl group by alkylation of a resultant benzylic anion. Hydrolysis of the sterically less hindered adducts gave the corresponding quaternary amino acids with no racemization, whereas hydrolytic ring opening gave the corresponding valine dipeptides from bulkier bislactims.
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19

García-López, José-Antonio, Meliha Çetin y Michael F. Greaney. "Double Heteroatom Functionalization of Arenes Using Benzyne Three-Component Coupling". Angewandte Chemie International Edition 54, n.º 7 (7 de enero de 2015): 2156–59. http://dx.doi.org/10.1002/anie.201410751.

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20

García-López, José-Antonio, Meliha Çetin y Michael F. Greaney. "Double Heteroatom Functionalization of Arenes Using Benzyne Three-Component Coupling". Angewandte Chemie 127, n.º 7 (7 de enero de 2015): 2184–87. http://dx.doi.org/10.1002/ange.201410751.

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21

Wei, Yong-Liang, Yue Li, Yun-Qi Chen, Ying Dong, Jia-Jia Yao, Xin-Yue Han y Yu-Bin Dong. "Pd(II)-NHDC-Functionalized UiO-67 Type MOF for Catalyzing Heck Cross-Coupling and Intermolecular Benzyne–Benzyne–Alkene Insertion Reactions". Inorganic Chemistry 57, n.º 8 (4 de abril de 2018): 4379–86. http://dx.doi.org/10.1021/acs.inorgchem.7b03271.

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22

Larrosa, Igor, Marianne I. Da Silva, Patricio M. Gómez, Peter Hannen, Eunjung Ko, Steven R. Lenger, Simon R. Linke, Andrew J. P. White, Donna Wilton y Anthony G. M. Barrett. "Highly Convergent Three Component Benzyne Coupling: The Total Synthesis ofent-Clavilactone B". Journal of the American Chemical Society 128, n.º 43 (noviembre de 2006): 14042–43. http://dx.doi.org/10.1021/ja0662671.

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23

Soorukram, Darunee, Tao Qu y Anthony G. M. Barrett. "Four-Component Benzyne Coupling Reactions: A Concise Total Synthesis of Dehydroaltenuene B". Organic Letters 10, n.º 17 (4 de septiembre de 2008): 3833–35. http://dx.doi.org/10.1021/ol8015435.

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24

Garcia-Lopez, Jose-Antonio, Meliha Cetin y Michael F. Greaney. "ChemInform Abstract: Double Heteroatom Functionalization of Arenes Using Benzyne Three-Component Coupling." ChemInform 46, n.º 25 (junio de 2015): no. http://dx.doi.org/10.1002/chin.201525067.

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25

Kan, Steven Z., Young C. Xu, Quan Chen y Ben S. Freiser. "Coupling reactions of Fe(benzyne)+ and Fe(naphthyne)+ in the gas phase". Journal of Mass Spectrometry 32, n.º 12 (diciembre de 1997): 1310–16. http://dx.doi.org/10.1002/(sici)1096-9888(199712)32:12<1310::aid-jms591>3.0.co;2-6.

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26

Frid, Michael, Dolores Pérez, Andrew J. Peat y Stephen L. Buchwald. "A Combined Zirconocene Benzyne−Palladium Cross-Coupling Route to Substituted Biphenyls and Terphenyls". Journal of the American Chemical Society 121, n.º 40 (octubre de 1999): 9469–70. http://dx.doi.org/10.1021/ja992345r.

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27

Retbøll, Mikael, Alison J. Edwards, A. David Rae, Anthony C. Willis, Martin A. Bennett y Eric Wenger. "Preparation of Benzyne Complexes of Group 10 Metals by Intramolecular Suzuki Coupling ofortho-Metalated Phenylboronic Esters: Molecular Structure of the First Benzyne-Palladium(0) Complex". Journal of the American Chemical Society 124, n.º 28 (julio de 2002): 8348–60. http://dx.doi.org/10.1021/ja0264091.

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28

Pineschi, Mauro, Francesco Berti, Paolo Crotti y Giulio Cassano. "Copper-Catalyzed Arylation of Alkenyl Aziridines via Three-Component Coupling Reaction involving Alkynes and Benzyne". Synlett 23, n.º 17 (21 de septiembre de 2012): 2463–68. http://dx.doi.org/10.1055/s-0031-1290467.

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29

Buchwald, Stephen L., Ann Sayers, Brett T. Watson y John C. Dewan. "The zirconocene induced coupling of benzyne with nitriles: Synthesis, structure and reactions of novel azametallacyclopentenes". Tetrahedron Letters 28, n.º 28 (enero de 1987): 3245–48. http://dx.doi.org/10.1016/s0040-4039(00)95483-2.

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30

Frid, Michael, Dolores Perez, Andrew J. Peat y Stephen L. Buchwald. "ChemInform Abstract: A Combined Zirconocene Benzyne-Palladium Cross-Coupling Route to Substituted Biphenyls and Terphenyls." ChemInform 31, n.º 4 (11 de junio de 2010): no. http://dx.doi.org/10.1002/chin.200004104.

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31

Bender, Christopher O., René T. Boeré, Peter W. Dibble y Ryan T. McKay. "Structures of the 2:1 adducts of benzyne with 2-methylanisole and benzene". Canadian Journal of Chemistry 85, n.º 7-8 (1 de julio de 2007): 461–65. http://dx.doi.org/10.1139/v07-058.

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The 2:1 adduct of benzyne with 2-methylanisole is shown to have the bisbenzotricyclic structure 6,6a,11,11a-tetrahydro-5-methoxy-6-methyl-5,6,11-metheno-5H-benzo[a]fluorene by a single-crystal X-ray diffraction study (C20H18O: Pca21, a = 15.0497(17), b = 9.87783(11), c = 9.6846(11); Z = 4; 1672 data points, R1 = 0.0325). This structure is compared to an unpublished crystal structure of the parent hydrocarbon 6,6a,11,11a-tetrahydro-5,6,11-metheno-5H-benzo[a]fluorene, C18H14. Both structures have also been computed by DFT methods at the B3LYP/6-311(d,p) level of theory. Bond distances and angles between the solid-state measurements and gas-phase calculations are found to agree well; average deviations are well below 1%. The 1H NMR spectra show surprisingly small 3JHH couplings in the central tricyclic cage, but can be assigned using 2D spectroscopy.Key words: Hydrocarbon cages, strained rings, cyclopropane, X-ray crystallography, NMR.
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32

Kotha, Raghavendhar R., Ravikiran Yerabolu, Duanchen Ding, Lucas Szalwinski, Xin Ma, Ashley Wittrig, John Kong, John J. Nash y Hilkka I. Kenttämaa. "Spin–Spin Coupling Between Two meta ‐Benzyne Moieties In a Quinolinium Tetraradical Cation Increases Their Reactivities". Chemistry – A European Journal 25, n.º 17 (25 de febrero de 2019): 4472–77. http://dx.doi.org/10.1002/chem.201806096.

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33

Aseman, Marzieh Dadkhah, Christina A. Roselli y Michel R. Gagné. "Promoting C–C Bond Coupling of Benzyne and Methyl Ligands in Electron-Deficient (triphos)Pt–CH3+ Complexes". Organometallics 34, n.º 12 (2 de junio de 2015): 2707–9. http://dx.doi.org/10.1021/acs.organomet.5b00121.

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34

Berti, Francesco, Paolo Crotti, Giulio Cassano y Mauro Pineschi. "ChemInform Abstract: Copper-Catalyzed Arylation of Alkenyl Aziridines via Three-Component Coupling Reaction Involving Alkynes and Benzyne." ChemInform 44, n.º 9 (26 de febrero de 2013): no. http://dx.doi.org/10.1002/chin.201309062.

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35

Nagaki, Aiichiro, Daisuke Ichinari y Jun-ichi Yoshida. "Three-Component Coupling Based on Flash Chemistry. Carbolithiation of Benzyne with Functionalized Aryllithiums Followed by Reactions with Electrophiles". Journal of the American Chemical Society 136, n.º 35 (25 de agosto de 2014): 12245–48. http://dx.doi.org/10.1021/ja5071762.

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36

Dupuis, Laurence, Nadine Pirio, Philippe Meunier, Alain Igau, Bruno Donnadieu y Jean-Pierre Majoral. "Zirconocen–Benzyme-Mediated Intramolecular Coupling of Bis(alkynyl)phosphane: A Way to Mono- and Tricyclic 1,2-Dihydrophosphetes". Angewandte Chemie International Edition in English 36, n.º 9 (16 de mayo de 1997): 987–89. http://dx.doi.org/10.1002/anie.199709871.

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37

Helgaker, Trygve y Michał Jaszuński. "Density-Functional and Coupled-Cluster Singles-and-Doubles Calculations of the Nuclear Shielding and Indirect Nuclear Spin−Spin Coupling Constants of o-Benzyne". Journal of Chemical Theory and Computation 3, n.º 1 (22 de noviembre de 2006): 86–94. http://dx.doi.org/10.1021/ct600234n.

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38

Nettles, Shawn M. y Jeffrey L. Petersen. "Synthesis and structural characterization of [(C5H4)SiMe2(N-t-Bu)]Ti[(o-C6H4)C(Ph)C(Ph)], generated via an alkyne-Ti benzyne coupling reaction". Journal of Organometallic Chemistry 692, n.º 21 (octubre de 2007): 4654–60. http://dx.doi.org/10.1016/j.jorganchem.2007.06.019.

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39

Zhang, Yajuan, Jie Dong, Yu Lei, Lingli Zong, Ke Zhang y Yimin Hu. "High Regioselectivity Ferrocenyl Cyclohexene/Cyclopentene Ferrocene Isomerization through Benzynes Transfer Coupling". Organic Chemistry Frontiers, 2023. http://dx.doi.org/10.1039/d2qo01836e.

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High regioselectivity Ferrocenyl cyclohexene/cyclopentene isomerization through hexadehydro-Diels-Alder (HDDA) benzyne transfer coupling was developed. The tetraynes result in the formation of an aryne through HDDA reaction which is then in situ...
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40

Jeganmohan, Masilamani, Sivakolundu Bhuvaneswari y Chien-Hong Cheng. "ChemInform Abstract: A Cooperative Copper- and Palladium-Catalyzed Three-Component Coupling of Benzynes, Allylic Epoxides, and Terminal Alkynes." ChemInform 40, n.º 20 (19 de mayo de 2009). http://dx.doi.org/10.1002/chin.200920062.

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41

Yang, Yun-Yun, Wang-Ge Shou y Yan-Guang Wang. "ChemInform Abstract: Tandem Coupling Reactions of Benzynes and 1,3-Diones: A Novel Synthesis of 2,2-Diphenyl-1,3-diones." ChemInform 39, n.º 9 (26 de febrero de 2008). http://dx.doi.org/10.1002/chin.200809108.

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42

Jayanth, Thiruvellore Thatai, Masilamani Jeganmohan y Chien-Hong Cheng. "Highly Efficient Route to o-Allylbiaryls via Palladium-Catalyzed Three-Component Coupling of Benzynes, Allylic Halides, and Aryl Organometallic Reagents." ChemInform 36, n.º 45 (8 de noviembre de 2005). http://dx.doi.org/10.1002/chin.200545110.

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43

BUCHWALD, S. L., B. T. WATSON, R. T. LUM y W. A. NUGENT. "ChemInform Abstract: A General Method for the Preparation of Zirconocene Complexes of Substituted Benzynes: in situ Generation, Coupling Reactions, and Use in the Synthesis of Polyfunctionalized Aromatic Compounds." ChemInform 19, n.º 10 (8 de marzo de 1988). http://dx.doi.org/10.1002/chin.198810300.

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44

Welsh, Erin N., Katherine N. Robertson y Alexander W. H. Speed. "Gram-Scale Synthesis of the N-Phenyl Phenothiazine Photocatalyst by Benzyne Addition". Canadian Journal of Chemistry, 3 de agosto de 2022. http://dx.doi.org/10.1139/cjc-2022-0139.

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N-phenyl phenothiazine is one of the most reducing photoredox catalysts. Its synthesis commonly requires transition metal catalyzed cross-coupling reactions. Here we show the syntheses of four aryl phenothiazines via a benzyne route, including a multi-gram scale synthesis of N-phenyl phenothiazine. While yields are modest, the simplicity, low cost, and lack of requirement for cross-coupling catalysts in this synthesis will be attractive to users of this photocatalyst.
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45

Henderson, Jaclyn L., Andrew S. Edwards y Michael F. Greaney. "Three-Component Coupling of Benzyne: Domino Intermolecular Carbopalladation." ChemInform 37, n.º 43 (24 de octubre de 2006). http://dx.doi.org/10.1002/chin.200643107.

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46

Larrosa, Igor, Marianne I. Da Silva, Patricio M. Gomez, Peter Hannen, Eunjung Ko, Steven R. Lenger, Simon R. Linke, Andrew J. P. White, Donna Wilton y Anthony G. M. Barrett. "Highly Convergent Three-Component Benzyne Coupling: The Total Synthesis of ent-Clavilactone B." ChemInform 38, n.º 11 (13 de marzo de 2007). http://dx.doi.org/10.1002/chin.200711207.

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47

Soorukram, Darunee, Tao Qu y Anthony G. M. Barrett. "ChemInform Abstract: Four-Component Benzyne Coupling Reactions: A Concise Total Synthesis of Dehydroaltenuene B." ChemInform 40, n.º 2 (13 de enero de 2009). http://dx.doi.org/10.1002/chin.200902205.

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48

BUCHWALD, S. L., A. SAYERS, B. T. WATSON y J. C. DEWAN. "ChemInform Abstract: The Zirconocene Induced Coupling of Benzyne with Nitriles: Synthesis, Structure, and Reactions of Novel Azametallacyclopentenes." ChemInform 18, n.º 51 (22 de diciembre de 1987). http://dx.doi.org/10.1002/chin.198751160.

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49

Black, Joshua Alexander, Alexander Waigum, Robert G. Adam, K. R. Shamasundar y Andreas Köhn. "Towards an efficient implementation of internally contracted coupled-cluster methods". Journal of Chemical Physics, 10 de marzo de 2023. http://dx.doi.org/10.1063/5.0143214.

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A new implementation of the internally contracted multireference coupled-cluster with singles and doubles (icMRCCSD) method is presented. The new code employs an efficient tensor contraction kernel and can also avoid full four-external integral transformations, which significantly extends the scope of the applicability of icMRCCSD. The new implementation is currently restricted to the simple case of two active electrons in two orbitals and also supports the computation of spin-adapted doublet and triplet coupled-cluster wavefunctions. This contribution describes the basic approach for the automated derivation of the working equations and benchmarks the current code against efficient implementations of standard methods such as single-reference coupled-cluster singles and doubles (CCSD) and internally contracted multireference configuration interaction (icMRCI). The run times for linearized variants of icMRCCSD are only twice as long as comparable CCSD runs and similar to those of the icMRCI implementation, while the non-linear terms of more complete variants of icMRCCSD lead to an order of magnitude longer computation times. Nevertheless the new code allows for computations at larger scales than it was possible previously, with less demands on memory and disk-space resources. This is exemplified by numerical structure optimizations and harmonic force field determinations of NC2H5 isomers and the singlet and triplet state of m-benzyne. In addition, the exchange coupling of a dinuclear copper complex is determined. This work also defines a new commutator approximation for icMRCCSD which includes all terms that are also present in the single-reference CCSD method, thus yielding a consistent pair of single-reference and multireference coupled-cluster methods.
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