Relevant bibliographies by topics / Aryne Chemistry

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Aryne Chemistry'

Author: Grafiati
Published: 6 September 2023

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Journal articles on the topic "Aryne Chemistry"

1

Brown, Roger F. C. "Flash Vacuum Pyrolytic Generation of Arynes - in Retrospect." Australian Journal of Chemistry 63, no. 7 (2010): 1002. http://dx.doi.org/10.1071/ch10086.

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The development of the chemistry of benzyne and of arynes under flash vacuum pyrolytic conditions was strongly influenced by a parallel study of the chemistry of propadienones, and by the discovery of the acetylene/methylenecarbene rearrangement. A limited range of typical aryne reactions studied at The Australian National University and at Monash University from 1965 to 1996 is described, and pathways of aryne formation are considered.
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Lee, Daesung, and Sourav Ghorai. "Aryne-Based Multicomponent Coupling Reactions." Synlett 31, no. 08 (March 20, 2020): 750–71. http://dx.doi.org/10.1055/s-0039-1690824.

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Multicomponent reactions (MCRs) constitute a powerful synthetic tool to generate a large number of small molecules with high atom economy, which thus can efficiently expand the chemical space with molecular diversity and complexity. Aryne-based MCRs offer versatile possibilities to construct functionalized arenes and benzo-fused heterocycles. Because of their electrophilic nature, arynes couple with a broad range of nucleophiles. Thus, a variety of aryne-based MCRs have been developed, the representative of which are summarized in this account.1 Introduction2 Aryne-Based Multicomponent Reactions2.1 Trapping with Isocyanides2.2 Trapping with Imines2.3 Trapping with Amines2.4 Insertion into π-Bonds2.5 Trapping with Ethers and Thioethers2.6 Trapping with Carbanions2.7 Transition-Metal-Catalyzed Approaches3 Strategies Based on Hexadehydro Diels–Alder Reaction3.1 Dihalogenation3.2 Halohydroxylation and Haloacylation3.3 Amides and Imides3.4 Quinazolines3.5 Benzocyclobutene-1,2-diimines and 3H-Indole-3-imines3.6 Other MCRs of Arynes and Isocyanides4 Conclusion
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Idiris, Fahima I. M., and Christopher R. Jones. "Recent advances in fluoride-free aryne generation from arene precursors." Organic & Biomolecular Chemistry 15, no. 43 (2017): 9044–56. http://dx.doi.org/10.1039/c7ob01947e.

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Aryne chemistry has flourished in the past few decades. This review highlights new aryne precursors that operate under fluoride-free conditions as alternative methodologies to the popular fluoride-mediated ortho-silylaryl triflates.
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Martin, Nelson, and Ruchi Bharti. "Arynes in Natural Product Synthesis." International Journal for Research in Applied Science and Engineering Technology 11, no. 4 (April 30, 2023): 2633–44. http://dx.doi.org/10.22214/ijraset.2023.50703.

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Abstract: Arynes are a unique class of intermediates used in synthetic organic chemistry, and research interest has been intensely focused on their peculiar reactivities. Arynes have been researched for almost a century. However, difficulties in monitoring these reactive species, as well as difficulties in creating synthetically viable techniques for their synthesis and trapping, have restricted their application. A key tactic for achieving the racemic and enantiopure total synthesis of a broad variety of natural compounds or their structural derivatives. The chemistry of arynes has advanced significantly over the past thirty years, particularly in the field of transition metal carbon- carbon and carbon-heteroatom bond-forming mechanisms. The field’s fast growth is largely attributable to the development of mild aryne production processes. To create a natural product with complex organic molecules, the role of aryne intermediates was non-replaceable. These organic substances are often used in medicine, therapies, or as raw material for the synthesis of other substances. Moreover, they may perform important biological tasks. There are numerous methods for synthesizing natural compounds including total synthesis, semi-synthesis, and biosynthesis. Total synthesis is the process of creating natural products entirely chemically from basic precursors as well as it can be produced in large quantities and can reveal information about its biological activity. One of the developments in Arynes’ chemistry is the chemical rearrangements brought about by this electrophilic intermediate. It is not feasible to use conventional methods in a single step. This review article discusses how arynes are used to create natural products. Arynes has a wide range of functionality in the field of scientific research. The evolution of this method has made a tremendous change in the total synthesis of natural products. Benzynes enabled creative synthesis in mild conditions. The transformation has expanded to investigate various reaction classes such as nucleophilic addition, (4+2), and (2+2) cycloaddition strategies and metal-catalyzed reactions are shown and explained in this article. This review will provide an idea about how the arynes act as an intermediate in those reaction mechanisms and enlighten the scope of these aryne intermediate.
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Neog, Kashmiri, and Pranjal Gogoi. "Recent advances in the synthesis of organophosphorus compounds via Kobayashi's aryne precursor: a review." Organic & Biomolecular Chemistry 18, no. 47 (2020): 9549–61. http://dx.doi.org/10.1039/d0ob01988g.

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Ito, Motoki, Yuka Yamabayashi, Mio Oikawa, Emi Kano, Kazuhiro Higuchi, and Shigeo Sugiyama. "Silica gel-induced aryne generation from o-triazenylarylboronic acids as stable solid precursors." Organic Chemistry Frontiers 8, no. 12 (2021): 2963–69. http://dx.doi.org/10.1039/d1qo00385b.

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We developed o-triazenylarylboronic acids as stable solid aryne precursors, which generate arynes under mild conditions using silica gel as the sole reagent and undergo reactions with a range of arynophiles both in solution and in the solid-state.
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Tanaka, Hideya, Hitoshi Kuriki, Teruhiko Kubo, Itaru Osaka, and Hiroto Yoshida. "Copper-catalyzed arylstannylation of arynes in a sequence." Chemical Communications 55, no. 46 (2019): 6503–6. http://dx.doi.org/10.1039/c9cc02738f.

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Diverse ortho-stannylbiaryls and teraryls have been synthesized by copper-catalyzed arylstannylation of arynes, in which the single or dual insertion of arynes into arylstannanes is precisely controllable by simply changing the equivalence of the aryne precursors employed.
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Nakajima, Hana, Yuki Hazama, Yuki Sakata, Keisuke Uchida, Takamitsu Hosoya, and Suguru Yoshida. "Diverse diaryl sulfide synthesis through consecutive aryne reactions." Chemical Communications 57, no. 21 (2021): 2621–24. http://dx.doi.org/10.1039/d0cc08373a.

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Wenk, Hans Henning, Michael Winkler, and Wolfram Sander. "One Century of Aryne Chemistry." Angewandte Chemie International Edition 42, no. 5 (February 3, 2003): 502–28. http://dx.doi.org/10.1002/anie.200390151.

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Mhaske, Santosh, and Ranjeet Dhokale. "Transition-Metal-Catalyzed Reactions Involving Arynes." Synthesis 50, no. 01 (November 22, 2017): 1–16. http://dx.doi.org/10.1055/s-0036-1589517.

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The plethora of transformations attainable by the transition-metal-catalyzed reactions of arynes has found immense contemporary interest in the scientific community. This review highlights the scope and importance of transition-metal-catalyzed aryne reactions in the field of synthetic organic chemistry reported to date. It covers transformations achieved by the combination of arynes and various transition metals, which provide a facile access to a biaryl motif, fused polycyclic aromatic compounds, different novel carbocycles, various heterocycles, and complex natural products.1 Introduction2 Insertion of Arynes3 Annulation of Arynes4 Cycloaddition of Arynes5 Multicomponent Reactions of Arynes6 Miscellaneous Reactions of Arynes7 Total Synthesis of Natural Products Using Arynes8 Conclusion
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Dissertations / Theses on the topic "Aryne Chemistry"

1

Cant, Alastair Alexander. "Investigations into aryne chemistry." Thesis, University of Edinburgh, 2012. http://hdl.handle.net/1842/6249.

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The first project in this thesis describes our research reacting arynes with tertiary allyl amines to generate functionalised anilines via a benzyne induced aza-Claisen reaction. This process works in good to excellent yields and the methodology can be further applied to make benzannulated medium sized ring amine systems. The second project covered in this thesis details our studies in the generation of benzyne from benzoic acid. This process utilises palladium catalysis involving an ortho C-H activation of benzoic acid which generates a 5 membered palladacycle. This palladacycle then spontaneously decomposes with heat to generate palladium bound benzyne and carbon dioxide. The yield of benzyne was monitored by observing the amount of triphenylene formed in the process. Further synthetic applications in this process were limited, but it was shown that the benzyne could be reacted with alkynes to generate phenanthrene and naphthalene products. The third project in this thesis details our work on the insertion of benzyne into the C–S bond of thioesters. Using palladium catalysis and an o-trimethylsilylphenyl triflate benzyne precursor, a variety of thioethers were produced. The yields for this reaction were moderate to good but it was found that only aromatic substituents were tolerated on the thioester.
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Liu, Zhijian. "Novel aryne chemistry in organic synthesis." [Ames, Iowa : Iowa State University], 2006.

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Pocock, Ian. "Novel cascade aryne-capture/rearrangement reactions." Thesis, University of Huddersfield, 2014. http://eprints.hud.ac.uk/id/eprint/23743/.

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Arynes are reactive intermediates that have been an academic curiosity for over a century. A recent renaissance of interest in the chemistry of these intermediates can be traced back to the development of ortho-(silyl)aryl triflates as aryne precursors. The application of aryne chemistry outside academia has been precluded by the expense and laborious preparation of these precursors. Diphenyliodonium-2-carboxylate has been shown to be a stable and inexpensive benzyne precursor, however application has been limited due to the high temperature (>160 ºC) and long reaction times required to generate benzyne by this protocol. Described within is an investigation whereby diphenyliodonium-2-carboxylate is successfully decomposed using microwave irradiation to generate benzyne. This proof of concept investigation shows diphenyliodonium-2-carboxylate can be applied as an off-the-shelf benzyne precursor; by using microwave radiation, significantly reduced reaction times and lower b.p. solvents can facilitate a more universal application of this protocol than previously described. The investigation into the reactions of allylamino malonates with arynes is also described. Simple allylamino malonates are shown to perform a novel cascade aryne capture/ring-closure/[2,3]-rearrangement to generate indolin-3-one products. The influence of substitution of the indolin-3-one products on the photophysical properties is probed. Tetrahydropyridine derived aminomalonates result in a ring contraction by [2,3]-rearrangement to N-phenyl pyrrolidine products. Further investigations show N-allyl proline methyl esters also generate indolin-3-one products by this novel cascade mechanism. The photophysical properties of these products are also probed. N-diallylalanine methyl ester is shown to generate indolin-3-one with benzyne however N-allyl sarcosine ethyl ester generates the N-phenyl -allylated amino esters product by aryne capture/[2,3]-rearrangement.
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Lin, Wenwei. "Preparation of Polyfunctionalized Grignard Reagents and their Application in Aryne Chemistry." Diss., [S.l.] : [s.n.], 2006. http://edoc.ub.uni-muenchen.de/archive/00006045.

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Schwan, Johannes [Verfasser]. "Step Efficient Synthesis of 3,4-Dioxygenated Quinolones Enabled by Aryne Chemistry / Johannes Schwan." Berlin : Freie Universität Berlin, 2020. http://d-nb.info/1219904783/34.

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Bates, Richard Simon. "Arene ruthenium chemistry." Thesis, University of Nottingham, 1990. http://eprints.nottingham.ac.uk/11890/.

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This thesis describes the synthesis and reactivity studies of new arene-ruthenium(II) and arene-ruthenium(O) complexes. Ultrasound has been investigated as an alternative energy source, with the overall aim of synthesising arene ruthenium clusters. Chapter 1 gives an introduction and summary of the known arene ruthenium chemistry reported to date. Chapter 2 reports the synthesis of (CGH6)Ru(C2H4)2 and (MeC6H4CHMe2)Ru(C2H4)2. Low temperature protonation studies generated (C6H6)Ru(H)(CZH4)2' and (MeC6H4CHMe2)Ru(H)(C2H4)7ý. These are observed by 1H nmr spectroscopy to undergo two dynamic processes, rotation of the ethylene ligands and an exchange between the hydride and the hydrogens of the ethylenes. On protonation with trifluoroacetic acid (C6H6)Ru(02CCF3)2 has been shown to be the final product. Nucleophilic substitution investigations of the bis(ethylene) complexes has determined that the arene is more labile than the coordinated ethylene. Chapter 3 reports the generation of a reactive intermediate, [(MeC6H4CHMez)Ru(THF)2]", and the reactions it undergoes. The synthesis and stereochemistry of the new complexes [(MeC6H4CHMe2)RuBr(C3H5)] and Ru(H)[(C6H40) (OPh)2][P(OPh)3]3 are reported. Chapter 4 describes the successful synthesis of the project goal, with the formation of the trimer [(MeC. H., CHMe2)3Ru3Se,_1` and the tetra nuclear species [(MeC6H4CHMe2)4Ru4H4]2'. Electrochemistry shows both complexes undergo two, one-electron reversible reductions to generate their neutral analogues. Ru3(CO)12 was formed when arene ruthenium carbonyl clusters were sought. Chapter 5 reports the formation and reactivity of arene ruthenium complexes containing nitrogen based ligands. The half sandwich complexes, (arene)RuCl2(NH2R) (arene = C6H6, R= Et, CMe, C6H4Me; McC6H4CHMe2, R=CMe3) and (C. H6)RuCl(NHZCGH4Me)Z' have been synthesised in good yield. However, these complexes are not synthetically useful as substrates for cluster synthesis, although (C6H6)RuC12(NH2CMe3) can be converted to the mixed ethoxide-halide dimer, [(C6H6)Ru(OEt)]2Cl`. Me3SiN3 on reaction with [(MeC6H4CHMe2)RuC12]2 affords [(MeC6H4CHMe2)RuCl(N3)]Z. An X-ray crystal structure determination of this complex showed the nitrogens bridging the two ruthenium atoms are pyramidal rather than the expected planar in geometry. [(MeC6H4CHMe2)RuCl(N3)]2 undergoes chloride loss to form the triply bridged dimer, [(MeCGH4CHMe2)RuCl(N3)z]', and bridge cleavage to form [(MeC, H4CHMe2)RuCl(N3)PPh3]. The latter complex is believed to undergo disproportionation in solution. Conclusions and future directions of the project are discussed in chapter. 6. The appendix provides a discussion of ultrasound proposed structure.
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Smith, Paul David. "Arene-ruthenium chemistry." Thesis, University of Nottingham, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.357040.

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Rooney, Aaron. "Asymmetric functionalisation in arene chromium tricarbonyl chemistry." Thesis, Imperial College London, 2007. http://hdl.handle.net/10044/1/11891.

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The research described in this thesis is concerned with the exploitation of a nonracemic chiral base to create enantiomerically enriched chiral centres on the benzylic positions of arene chromium tricarbonyl complexes. The first chapter is in two parts. The first part contains a historical overview of chiral bases and their use in asymmetric synthesis, as well as demonstrating the versatility of chiral base reactions. The latter part deals with the chemistry of arene chromium tricarbonyl complexes and how these molecules have been used in asymmetric synthesis and as ligands in asymmetric catalysis. The second chapter looks at the synthesis of a novel benzyl phosphine chromium tricarbonyl complex and attempts to asymmetrically deprotonate the molecule in order to create a new chiral monophosphine. The third chapter describes the generation of a range of novel monophosphine ligands, based on an arene chromium tricarbonyl core, by exploitation of an asymmetric deprotonationlelectrophilic quench sequence. the novel monophosphines have been assayed in the asymmetric hydrosilylation reaction, and the results are presented and discussed. The fourth chapter is a study of arene chromium tricarbonyl complexes of dibenzyl ethCl and a dibclIzy laminc, dnd their as) mmetr ie dept otonatiol'l. The genet [tHon of new C2-symmetric ethers with high enantioselectivity is demonstrated. The fifth chapter describes the attempted construction of a novel chiral C3-symmetric triol using the chiral base mediated asymmetric benzylic functionalisation approach. The sixth chapter contains the experimental details of the work presented in Chapters two, three, four and five. Chapter seven provides the bibliographic information.
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Lough, Julie Ann. "Aqueous solution chemistry of ruthenium arene anticancer complexes." Thesis, University of Warwick, 2010. http://wrap.warwick.ac.uk/35524/.

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Metal complexes currently are currently of much interest in the field of anticancer drug development. Platinum complexes such as cisplatin, are now widely used in the clinic and have led to a focus on the synthesis of new classes of other metal-based complexes, such as ruthenium anticancer drugs. In order to understand the mechanism of action of these complexes and to improve structureactivity relationships thereof, a comprehensive study of the solution chemistry is important. In this thesis the mechanism and kinetic detail of the exchange of amino protons on one such class of complex, [(η6-biphenyl)Ru(N,N’- ethylenediamine)Cl]+ was investigated in detail. Stereospecific assignment of NH protons was carried out by NOESY NMR on a pyridine adduct [(η6- biphenyl)Ru(N,N’-ethylendiamine)(N-pyridine)]2+. Using 1H and 2H NMR spectroscopy, rates of exchange were observed at different pH values, temperatures and ionic strengths a series of N-H/2H exchange reactions were studied and the data collected. The data are consistent with an exchange mechanism involving proton abstraction from the amine, followed by favourable reprotonation on the lowerface (relative to the overhanging arene) of the Ru(N,N’- ethylendiamine) five membered ring. In chlorido complexes this leads to the exchange of lower proton at a rate of three times that of those on the upperface at 298 K. To investigate the effects of electron density on the ruthenium on the exchange rates a series of π-donor pyridine ligands (pyridine, 4-methylpyridine, 4- tert-butylpyridine, and 4-methoxypyridine) in the place of the chloride were studied. The exchange rates were also investigated and showed a correlation between the basicity of the pyridine derivative and the favourability of exchange on the lower face, increasing this bias upto 11 fold. Density functional theory calculations suggests that there is an overlap between the p-orbital of the (ethylenediamine) nitrogen and the π*-antibonding orbital on the Ru-N(Pyridine) bond and σ*- antibonding orbital on the Ru-Cl bond, in their respective complexes. This overlap is proposed as a stabilising force on the deprotonated nitrogen allowing for a negative charge to be more stabile in one lobe of the p-orbital preferential to another. Following abstraction of the proton, the lone pair on the nitrogen is stabilised by an antibonding orbital, the top face less is susceptible to proton addition. Since DNA is a potential target for these complexes, the changes in shape induced by metal binding were investigated using Ion-Mobility Mass Spectrometry for the first time. Also in this work, the first ion-mobility mass spectrometry studies of the collisional cross sections (CCSs) of small complexes (<100 Å2) is also presented. This was developed using a new glycine based calibrant. Following binding of [(η6-biphenyl)Ru(N,N’- ethylenediamine)Cl]+ to the DNA hexamer d(CACGTG) changes in CCS values between ruthenated and non-ruthenated hexamers were studied. The change in CCS between these was not additive and suggestive of some folding or intercalation occurring upon ruthenium binding. Finally, attempts were madeto investigate shape change induced in DNA by binding to cisplatin using Förster Resonance Energy Transfer Methods are described. To date these results are inconclusive but work in this field is ongoing.
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Mehnert, Christian P. "Organometallic chemistry of molybdenum and iron and related studies." Thesis, University of Oxford, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.318895.

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Books on the topic "Aryne Chemistry"

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Mortier, Jacques, ed. Arene Chemistry. Hoboken, NJ: John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781118754887.

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D, Astruc, ed. Modern arene chemistry. Weinheim: Wiley-VCH, 2002.

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Appelbe, Ruth. Synthetic applications of cationic arene-alkene cyclisations. Dublin: University College Dublin, 1997.

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Peter, Kündig E., and Böttcher A, eds. Transition metal arene [pi]-complexes in organic synthesis and catalysis. Berlin: Springer-Verlag, 2004.

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Biju, Akkattu T. Modern Aryne Chemistry. Wiley & Sons, Incorporated, John, 2021.

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Biju, Akkattu T. Modern Aryne Chemistry. Wiley & Sons, Incorporated, John, 2021.

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Biju, Akkattu T. Modern Aryne Chemistry. Wiley & Sons, Incorporated, John, 2021.

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Biju, Akkattu T. Modern Aryne Chemistry. Wiley & Sons, Limited, John, 2021.

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Comprehensive Aryne Synthetic Chemistry. Elsevier, 2022. http://dx.doi.org/10.1016/c2020-0-01658-0.

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Yoshida, Hiroto. Comprehensive Aryne Synthetic Chemistry. Elsevier, 2022.

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Book chapters on the topic "Aryne Chemistry"

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Sanz, Roberto, and Anisley Suárez. "The Chemistry of Arynes." In Arene Chemistry, 299–336. Hoboken, NJ: John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781118754887.ch12.

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Winkler, Michael, Hans Henning Wenk, and Wolfram Sander. "Arynes." In Reactive Intermediate Chemistry, 741–94. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2005. http://dx.doi.org/10.1002/0471721492.ch16.

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Klumpp, Douglas A. "Electrophilic Aromatic Substitution." In Arene Chemistry, 1–31. Hoboken, NJ: John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781118754887.ch1.

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Rossi, Roberto A., Javier F. Guastavino, and María E. Budén. "Radical-Nucleophilic Aromatic Substitution." In Arene Chemistry, 243–68. Hoboken, NJ: John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781118754887.ch10.

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Mąkosza, Mieczysław. "Nucleophilic Substitution of Hydrogen in Electron-Deficient Arenes." In Arene Chemistry, 269–98. Hoboken, NJ: John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781118754887.ch11.

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Foubelo, Francisco, and Miguel Yus. "Reduction/Hydrogenation of Aromatic Rings." In Arene Chemistry, 337–64. Hoboken, NJ: John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781118754887.ch13.

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Kholdeeva, Oxana A. "Selective Oxidation of Aromatic Rings." In Arene Chemistry, 365–98. Hoboken, NJ: John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781118754887.ch14.

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Pigge, F. Christopher. "Dearomatization Reactions." In Arene Chemistry, 399–423. Hoboken, NJ: John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781118754887.ch15.

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Sankararaman, Sethuraman. "Aromatic Compounds Via Pericyclic Reactions." In Arene Chemistry, 425–49. Hoboken, NJ: John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781118754887.ch16.

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de Koning, Charles B., and Willem A. L. van Otterlo. "Ring-Closing Metathesis." In Arene Chemistry, 451–84. Hoboken, NJ: John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781118754887.ch17.

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Conference papers on the topic "Aryne Chemistry"

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Yus, M., J. Almena, E. Alonso, F. Alonso, A. Bachki, P. Choudhury, F. Foubelo, et al. "Functionalized Organolithium Compounds Through an Arene-Catalyzed Lithiation." In The 1st International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 1997. http://dx.doi.org/10.3390/ecsoc-1-02003.

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Gómez-Escalonilla, Maria José, Fernando Langa, Alejandro Criado, María Vizuete, Sergio García-Rodríguez, Jose Luis G. Fierro G. Fierro, Agustín Cobas, Diego Peña, and Enrique Guitián. "EfficientCycloaddition of Arynes to Carbon Nanotubes under Microwave Irradiation." In The 17th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2013. http://dx.doi.org/10.3390/ecsoc-17-c006.

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Yus, M., E. Alonso, F. Alonso, A. Bachki, K. Choudhury, F. Foubelo, C. Gomez, et al. "The Lithium-arene (cat.) System: New Applications to Organic Transformations." In The 2nd International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 1998. http://dx.doi.org/10.3390/ecsoc-2-01679.

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Yus, M., F. Alonso, P. Candela, C. Gomez, J. Gomis, A. Guijarro, F. Huerta, et al. "Nickel-promoted Reductive Cleavage of Nitrogen-nitrogen and Nitrogenoxygen Bonds Mediated by Lithium and a Catalytic Amount of an Arene or Polymer Supported Arene." In The 4th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01800.

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Yus, M., E. Alonso, J. Ferrandez, F. Foubelo, I. Gomez, D. Guijarro, A. Gutierrez, et al. "Arene-Catalysed Reductive Cleavage of the Benzylic Carbon-Sulfur Bond: Generation of Benzylic Lithium Reagents." In The 4th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01801.

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Nayak, Manini, Kanyanjali Samal, and Anita Pati. "Synthesis and characterization of the rccc-isomer of dodecatriazolo-resorcin[4]arene cavitand." In 2ND INTERNATIONAL CONFERENCE ON EMERGING SMART MATERIALS IN APPLIED CHEMISTRY (ESMAC-2021): ESMAC-2021. AIP Publishing, 2023. http://dx.doi.org/10.1063/5.0127510.

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Vavilova, A. A., I. E. Shiabiev, P. L. Padnya, and I. I. Stoikov. "Synthesis and spatial structure of p-tert-butylthiacalix[4]arene derivatives containing amide and amino groups." In ACTUAL PROBLEMS OF ORGANIC CHEMISTRY AND BIOTECHNOLOGY (OCBT2020): Proceedings of the International Scientific Conference. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0075982.

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Radivoy, Gabriel, Francisco Alonso, Miguel Yus, Viviana Dorn, Adriana Pierini, Andrés Ciolino, Yanina Moglie, and Fabiana Nador. "Reductive amination of aldehydes using a lithium-arene(cat.) reducing system. A simple one-pot procedure for the synthesis of secondary amines." In The 15th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2011. http://dx.doi.org/10.3390/ecsoc-15-00678.

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Yakimova, Luidmila, Aigul Nugmanova, Dmitry Shurpik, Pavel Padnya, Timur Mukhametzyanov, and Ivan Stoikov. "Micelleplexes and polyplexes with DNA from salmon sperm based on pillar[5]arenes and thiacalix[4]arene." In ACTUAL PROBLEMS OF ORGANIC CHEMISTRY AND BIOTECHNOLOGY (OCBT2020): Proceedings of the International Scientific Conference. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0069054.

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Reports on the topic "Aryne Chemistry"

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Liu, Zhijian. Novel Aryne Chemistry in Organic Synthesis. Office of Scientific and Technical Information (OSTI), December 2006. http://dx.doi.org/10.2172/897369.

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