Academic literature on the topic '[4+2] cycloaddition reaction'

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Journal articles on the topic "[4+2] cycloaddition reaction"

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Grygorenko, Oleksandr O., Viktoriia S. Moskvina, Oleksandr V. Hryshchuk, and Andriy V. Tymtsunik. "Cycloadditions of Alkenylboronic Derivatives." Synthesis 52, no. 19 (2020): 2761–80. http://dx.doi.org/10.1055/s-0040-1707159.

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The literature on cycloaddition reactions of boron-containing alkenes is surveyed with 132 references. The data are categorized according to the reaction type ([2+1], [2+2], [3+2], [4+2], and [4+3] cycloadditions). The cyclopropanation and the Diels–Alder reactions of alkenylboronic derivatives have been studied more or less comprehensively, and for some substrates, they can be considered as convenient methods for the rapid regio- and stereoselective construction of even complex cyclic systems. Other types of the cycloadditions, as well as mechanistic aspects of the processes, have been addres
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Winne, Johan, Jan Hullaert, Bram Denoo, Mien Christiaens, and Brenda Callebaut. "Heterocycles as Moderators of Allyl Cation Cycloaddition Reactivity." Synlett 28, no. 18 (2017): 2345–52. http://dx.doi.org/10.1055/s-0036-1588511.

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For the rapid elaboration of polycarbocyclic scaffolds, prevalent in many important families of terpenoid natural products, allyl cations derived from simple heterocyclic alcohols can be used as versatile reaction partners in both (4+3) and (3+2) cycloaddition pathways. Our recent progress in this area is outlined, pointing towards the untapped potential of heterocycles to act as reagents in novel or known but challenging organic transformations.1 Heterocyclic Reagents2 Cycloadditions and Allyl Cations3 Furfuryl Cations in Cycloadditions4 Heterocycle-Substituted Cations in Cycloadditions5 Mech
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Harmata, Michael, and Aswin Garimalla. "Derivatives of Alkyl 2-Hydroxy-3-oxocyclopent-1-enecarboxylates and Intermolecular [4+2] Cycloadditions of Cyclopentadienones Prepared Therefrom." Synthesis 50, no. 22 (2018): 4483–89. http://dx.doi.org/10.1055/s-0037-1610184.

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Some derivatives of alkyl 2-hydroxy-3-oxocyclopent-1-enecarboxylates have been synthesized and their reactivity as progenitors of cyclopentadienones for intermolecular [4+2]-cycloaddition reactions has been evaluated. It was found that the derivative containing a phosphate ester leaving group gave better yields in the cycloaddition reaction among the derivatives studied. The yields of the cycloaddition reactions were moderate, perhaps due side reactions not leading to the reactive intermediate cyclopentadienone.
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Newton, Rebecca, and G. Paul Savage. "Regioselective 1,3-Dipolar Cycloaddition Reactions of 4-Methylene-2-oxazolidinones with Benzonitrile Oxide." Australian Journal of Chemistry 61, no. 6 (2008): 432. http://dx.doi.org/10.1071/ch08111.

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Substituted 4-methylene-2-oxazolidinones were prepared in two steps by cyclizing O-propargyl carbamates, which in turn were prepared from propargyl alcohols and phenyl isocyanate. The 4-methylene-2-oxazolidinones underwent a 1,3-dipolar cycloaddition reaction with benzonitrile oxide to give the corresponding spiro heterocycles. Where the substitution pattern on the oxazolidinone engendered facial asymmetry, the cycloadditon reaction proceeded with 5:1 selectivity for the less hindered face of the dipolarophile.
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Burger, Klaus, Eva Höß, Norbert Sewald, Klaus Geith, Jürgen Riede, and Peter Bissinger. "Zum Cycloadditionsverhalten von 5-Azido-4-trifluormethyl-1,3-azolen / Cycloaddition Reactions with 5-Azido-4-trifluoromethyl-1,3-azoles." Zeitschrift für Naturforschung B 45, no. 12 (1990): 1695–708. http://dx.doi.org/10.1515/znb-1990-1217.

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[3+2] Cycloaddition reactions of 5-azido-4-trifluoromethyl-1,3-azoles with various CC multiple bond systems are described. On reaction of 5-azido-4-trifluoromethylthiazoles 2 with 2,3-dimethylbuta-1,3-diene no [3+2] cycloaddition products could be isolated, 5,6-dihydro-2 H-pyrane 19 was formed exclusively. Photolysis of 1,2,3-triazoles 23, 24, obtained from 2 and electron deficient alkynes, yields imidazo[5,1-b]thiazoles 28. This photoreaction can be interpreted mechanistically as a “Thio-Cornforth-Reaction”.
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Li, Jian, Shangrong Zhu, Qiuneng Xu, Li Liu, and Shenghu Yan. "Brønsted acid mediated intramolecular cyclopropane ring expansion/[4 + 2]-cycloaddition." Organic & Biomolecular Chemistry 17, no. 47 (2019): 10004–8. http://dx.doi.org/10.1039/c9ob02379h.

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A cascade reaction of 3-hydroxy-2-phenylisoindolin-1-one and cyclopropyl ketone has been developed via BrØnsted acid-promoted ring-opening/intramolecular cross-cycloaddition/[4 + 2]-cycloaddition process.
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Wiberg, N., G. Preiner, G. Wagner, and H. Köpf. "Reaktivität des labilen, durch Adduktbildung mit Ph2C=NSiMe3 gespeicherten Silaethens Me2Si=C(SiMe3)2 / Reactivity of the Labile Silaethene Me2Si = C(SiMe3)2, Stored as Ph2C =NSiMe3 Adducts." Zeitschrift für Naturforschung B 42, no. 9 (1987): 1062–74. http://dx.doi.org/10.1515/znb-1987-0902.

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Silaethene Me2Si = C(SiMe3)2 (1), stored as Ph2C=NSiMe3 adducts and regenerated from the adducts at about 100 °C as a reaction intermediate, combines with reactants a-b (e. g. HO-H, RO-H. RCOO-H, RS-H. RHN-H, Ph2CN-H, RO-SiR3, R2N-SiR3, Ph2CN-SiR3, Cl-GeR3, Cl-SnR3) with insertion into the a-b bond, with a=b (e.g. 0 = CPh2, Me3SiN = CPh2, CH2=CHOMe, cis-piperylene), a=b=c (e.g. RN = N = N, O = N=N). a=b-c=d (e.g. butadiene, isoprene, trans-piperylene, 2,3-dimethylbutadiene, cyclopentadiene, anthracene, benzophenone, N-trimethylsilylbenzophenoneimine) under [2+2]-, [2+3]- as well as [2+A]-cyclo
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Choi, Cheol Ho, and Mark S. Gordon. "Cycloaddition Reactions of Dienes on the SI(100)-2 × 1 Surface." International Journal of Modern Physics B 17, no. 08n09 (2003): 1205–10. http://dx.doi.org/10.1142/s0217979203018752.

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Quantum mechanical methods were adopted to study the surface reaction mechanisms of 1, 3-cyclohexadiene and acrylonitrile on the Si(100)-2x1 surface. According to the computed potential energy surfaces, both ⌊4+2⌋ and ⌊2+2⌋ cycloaddition products resulting from the reactions of surface dimers are possible due to the negligible activation barriers at the surface. Isomerization reactions among the surface products are very unlikely due to the predicted large activation barriers preventing thermal redistributions of the surface products. As a result, the distribution of the final surface products
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Kitagaki, Shinji, Yuki Okumura, and Chisato Mukai. "Reaction of ene-bis(phosphinylallenes): [2+2] versus [4+2] cycloaddition." Tetrahedron 62, no. 44 (2006): 10311–20. http://dx.doi.org/10.1016/j.tet.2006.08.083.

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Wu, Di, Rakesh Ganguly, Yongxin Li, Sin Ni Hoo, Hajime Hirao, and Rei Kinjo. "Reversible [4 + 2] cycloaddition reaction of 1,3,2,5-diazadiborinine with ethylene." Chemical Science 6, no. 12 (2015): 7150–55. http://dx.doi.org/10.1039/c5sc03174e.

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Dissertations / Theses on the topic "[4+2] cycloaddition reaction"

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Allart, Eric A. "Metal-promoted [3+2] and [4+2] cycloaddition reactions." Thesis, Loughborough University, 2008. https://dspace.lboro.ac.uk/2134/33615.

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Dicobalt complexes have been extensively used in synthetic chemistry to protect triple bonds, to form new carbon/carbon bonds using the Nicholas reaction and to form polycyclic molecules using the Pauson-Khand reaction. Using these dicobalt complexes, the formation of new carbon-heteroatom bonds was developed through [3+2] and [4+2] cycloaddition reactions via a stabilised dipole intermediate. Initial work carried out makes use of cyclopropanes substituted with a metal-alkyne complex towards the synthesis of tetrahydrofurans and pyrrolidines in good yields and with acceptable diastereoselectiv
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Linaza, Sabin. "Catalytic properties of antibodies in [4+2] cycloaddition." Thesis, University of Strathclyde, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.248702.

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Stones, James Alexander. "[4+2] cycloaddition reactions of conformationally restricted tethered trienes." Thesis, Imperial College London, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.338511.

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Ahmed, Awais. "[4+2] and [4+3] cycloaddition reactions and Lewis acid catalysed cycloisomerisation of malonyl epoxides." Thesis, Loughborough University, 2003. https://dspace.lboro.ac.uk/2134/12572.

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Donor-acceptor cyclopropanes have been extensively used in synthetic chemistry in [3+2] and [3+3] cycloaddition reactions for the preparation of highly substituted carbo- and heterocyclic products. This methodology is further extended to donor-acceptor cyclobutane in [4+2] and [4+3] cycloaddition reactions for the synthesis of highly substituted carbo- and heterocyclic products. Initial work carried out makes use of cyclobutanes substituted with a metal-alkyne complex towards the synthesis of tetrahydropyrans in good yields and with acceptable diastereoselectivity. The initial aim of the proje
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STAMMLER, ROBERT. "Approche aux squelettes aphidicolane et stemodane via une reaction tandem de cycloadditions (2+2+2) et (4+2)." Paris 6, 1992. http://www.theses.fr/1992PA066335.

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La decouverte d'activites biologiques associee a celle de nouvelles structures souleve un regain d'interet dans l'etude des diterpenes tetracycliques. C'est le cas de l'aphidicoline, premier membre d'une nouvelle famille, isolee en 1972, et revelant une forte activite contre le virus herpes simplex. Par la suite, d'autres composes naturels appartenant aux familles aphidicolane et stemodane se sont egalement reveles biologiquement actifs. L'objectif de notre travail consiste donc a proposer un schema reactionnel rapide permettant d'acceder a chacune des deux familles et a chacun des produits na
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Guillam, Anne. "Synthèse et cycloadditions [4+2] des 1,4-dialkoxybutadiènes." Rouen, 1997. http://www.theses.fr/1997ROUES078.

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Ce travail présente une étude générale de la réactivité des 1,4-dialkoxybutadiènes dans les cycloadditions [4+2]. La synthèse des précurseurs diéniques nécessaires à cette étude, a dans un premier temps, été mise au point par élimination conjuguée sur des acétals ,-insaturés -in-saturés. Les diènes dioxygénés désirés ont ainsi été obtenus de façon efficace et stéréocontrôlée. Ils présentent la configuration 1Z,3E très majoritaire. Cette approche a également permis la synthèse de nouveaux systèmes bisdiéniques trioxygénés. Les diènes précédents ont ensuite été engagés dans des réactions de Diel
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Chabour, Ihssene. "1,3-Dipolar cycloadditions using catalysts with double chirality and novel multicomponent [4+2] processes." Doctoral thesis, Universidad de Alicante, 2021. http://hdl.handle.net/10045/114674.

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In this thesis, different cycloaddition reactions, such as the enantioselective 1,3-dipolar-cycloaddition, which takes place between in situ generated stabilized azomethine ylides, and electrophilic alkenes, and the diastereoselective multicomponent reactions Amine-Aldehyde-Dienophile (AAD) or Phosphoramidate-Aldehyde-Dienophile (PAD) are described. In Chapter 1, an asymmetric 1,3-dipolar cycloaddition reaction involving an imino ester with tert-butyl acrylate was carried out using a silver(I) complex with double chirality, formed from a chiral phosphoramidite and chiral silver binolphosphate(
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PAPARIN, JEAN-LAURENT. "Developpement des reactions de cycloaddition 4 + 2 et 4 + 3 pour la preparation d'heterocycles azotes originaux utilisables en chimie combinatoire." Rennes 1, 1999. http://www.theses.fr/1999REN10192.

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Le travail presente dans ce memoire concerne la synthese de nouveaux scaffolds utilisables en chimie combinatoire. Une etude de la reaction d'aza diels-alder thermique de 1,4-bis aryl-2-aza-1,3-butadienes et de dienophiles deficients en electron a ete realisee. Les 2,5-bis aryl-pyridines cibles ont ete obtenues avec des rendements modestes. Une reaction competitive de dimerisation de l'azadiene a ete mise en evidence dans certains cas. Une etude de la reaction de cycloaddition 4 + 3 de diverses ,'-dibromocetones avec le n-carbomethoxypyrrole puis le n-carbomethoxy-2-(1',3'-dioxolan-2'-yl)-pyrr
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Black, Elzie Dewayne. "An investigation of a novel phase transfer system - the Omega Phase : the synthesis and [4&2] cycloaddition reactions of chiral 2-phenylpropanthial." Diss., Georgia Institute of Technology, 1988. http://hdl.handle.net/1853/27308.

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Chen, Xi. "Réactivité d’alcynes fonctionnalisés en présence d’or et d’argent : réactions de cycloadditions énantiosélectives et d'oxofluoration." Thesis, Université Côte d'Azur, 2020. http://www.theses.fr/2020COAZ4065.

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Dans le contexte de «chimie verte», le développement de systèmes catalytiques efficaces, propres et réalisés dans des conditions douces est fondamental en chimie organique. Ce manuscrit est divisé en trois chapitres. Le premier chapitre relate la bibliographie concernant la chimie de l’or et de l’argent lorsqu’ils sont en présence d’alcynes. Les exemples les plus significatifs et les plus proches de notre étude sont présentés. La suite du manuscrit présente les réactions de cycloaddition des enynes-1,6 catalysées par des complexes d’or et d’argent. Le troisième chapitre repose sur l’associatio
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Books on the topic "[4+2] cycloaddition reaction"

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UV-VIS SPECTROSCOPY OF 2, 4, 6-TRINITROTOLUENE-HYDROXIDE REACTION... U.S. DEPARTMENT OF DEFENSE... AUGUST 2002. s.n., 2003.

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United States. Army. Corps of Engineers, ed. UV-VIS SPECTROSCOPY OF 2, 4, 6-TRINITROTOLUENE-HYDROXIDE REACTION... U.S. DEPARTMENT OF DEFENSE... AUGUST 2002. s.n., 2003.

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United States. Army. Corps of Engineers, ed. UV-VIS SPECTROSCOPY OF 2, 4, 6-TRINITROTOLUENE-HYDROXIDE REACTION... U.S. DEPARTMENT OF DEFENSE... AUGUST 2002. s.n., 2003.

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United States. Army. Corps of Engineers, ed. UV-VIS SPECTROSCOPY OF 2, 4, 6-TRINITROTOLUENE-HYDROXIDE REACTION... U.S. DEPARTMENT OF DEFENSE... AUGUST 2002. s.n., 2003.

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Theresa, Reinold. Part 1 The Cold War Era (1945–89), 31 South African Incursions into Lesotho—1982. Oxford University Press, 2018. http://dx.doi.org/10.1093/law/9780198784357.003.0031.

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This chapter discusses the legality of South Africa’s incursion in Lesotho in 1982. After describing the facts of the case, it presents the legal arguments of the main protagonists – South Africa and Lesotho - and canvasses the positions taken by the UN General Assembly, the UN Security Council, as well as other important diplomatic players. It then assesses the legality of the intervention and discusses its impact on the progressive development of international law. It concludes that the incursion violated Article 2(4) of the UN Charter and that, in light of the overwhelmingly negative intern
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Konopasek, Lyuba, Marcy Rosenbaum, John Encandela, and Kathy Cole-Kelly. Evaluating communication skills training courses. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198736134.003.0062.

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This chapter describes strategies for designing programme evaluation for communication skills training courses. It draws on the communication literature to demonstrate evaluation approaches including use of control groups, validated instruments, and observation methods. The logic model is introduced as a tool to ensure that evaluation is aligned with programme plans. Kirkpatrick’s four levels of programme evaluation are used to analyse training outcomes. Kirkpatrick’s Level 1 evaluates learners’ reaction to training. Level 2 evaluates changes in the learners’ attitudes, such as self-efficacy,
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Paintal, Harman S., and Rajinder K. Chitkara. Zoonotic infections with filarial nematodes. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780198570028.003.0067.

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Filarial nematodes have been known to cause human disease for many centuries. Lymphatic filariasis is a common disease in the developing part of the world and much has been written about diagnosis and treatment of this scourge. Wuchereria , Brugia and Onchocerca (especially O. volvulus) have a wide pattern of distribution with severe morbidity. Given the years of scientific work in this field, many drugs that work against these parasites are available today and are attempting to control these infections. In this chapter, the focus is on those filarial nematodes that do not have humans as their
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Book chapters on the topic "[4+2] cycloaddition reaction"

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Baiazitov, Ramil Y., and Scott E. Denmark. "Tandem [4+2]/[3+2] Cycloadditions." In Methods and Applications of Cycloaddition Reactions in Organic Syntheses. John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118778173.ch16.

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Kester, Robert F., Steven J. Berthel, and Fariborz Firooznia. "[4+2] Cycloaddition Reactions of Indole Derivatives." In Topics in Heterocyclic Chemistry. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/7081_2010_55.

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Bur, Scott, and Albert Padwa. "[4+2] Cycloaddition Chemistry of Substituted Furans." In Methods and Applications of Cycloaddition Reactions in Organic Syntheses. John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118778173.ch13.

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Kunz, Horst, Bernd Müller, Waldemar Pfrengle, Karola Rück, and Wolfgang Stähle. "Carbohydrates as Chiral Templates in Stereoselective [4 + 2] Cycloaddition Reactions." In ACS Symposium Series. American Chemical Society, 1992. http://dx.doi.org/10.1021/bk-1992-0494.ch009.

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Halevi, E. Amitai. "Cycloadditions and Cycloreversions I. [2+2]-Cycloaddition." In Orbital Symmetry and Reaction Mechanism. Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-83568-1_6.

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Kurahashi, Takuya, and Seijiro Matsubara. "[4 + 2] and [3 + 2] Cycloaddition via Metallacycles." In Transition-Metal-Mediated Aromatic Ring Construction. John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118629871.ch12.

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Zhao, Da. "Reaction of o-Carboryne with Nitrones: A Formal [5 + 2] Cycloaddition." In Functionalization of Carborane via Carboryne Intermediates. Springer Singapore, 2016. http://dx.doi.org/10.1007/978-981-10-1569-4_4.

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D'Auria, M., L. Emanuele, and R. Racioppi. "1, 2-Cycloaddition Reaction of Carbonyl Compounds and Pentaatomic Heterocyclic Compounds." In Advances in Photochemistry. John Wiley & Sons, Inc., 2005. http://dx.doi.org/10.1002/0471714127.ch3.

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Gallego, Mar Gómez, and Miguel A. Sierra. "Level 3 - Case 37 Base-promoted HF Elimination from 4-Fluoro-4-(4’nitrophenyl)butan-2-one." In Organic Reaction Mechanisms. Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-642-18788-9_37.

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Jones, Darin E., and Michael Harmata. "Application of The [4+3] Cycloaddition Reaction To The Synthesis of Natural Products." In Methods and Applications of Cycloaddition Reactions in Organic Syntheses. John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118778173.ch19.

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Conference papers on the topic "[4+2] cycloaddition reaction"

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Peña-Gallego, A., J. Rodríguez-Otero, and E. M. Cabaleiro-Lago. "The influence of BF3 on the reaction path of the [4 + 2] cycloaddition of vinylketene with formaldimine. A computational study." In The 10th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2006. http://dx.doi.org/10.3390/ecsoc-10-01455.

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Doležal, Rafael, Natálie Karásková, Nadezhda V. Maltsevskaya, and Karel Kolář. "SUPPORTING CONCEPTUAL LEARNING IN ORGANIC CHEMISTRY THROUGH SEMI-EMPIRICAL MOLECULAR MODELING: HEURISTICS OF DIELS-ALDER [4+2] CYCLOADITIONS FOR PREPARATION OF POTENTIAL TLR4 MODULATORS." In Proceedings of the 2nd International Baltic Symposium on Science and Technology Education (BalticSTE2017). Scientia Socialis Ltd., 2017. http://dx.doi.org/10.33225/balticste/2017.39.

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A vast majority of novices in universities predominantly utilize algorithmic mental processes to resolve assigned tasks and tests. Although algorithmic thinking is an essential part of human cognitive functions, experts on didactics call for methods, which develop also conceptual thinking in beginners. Currently, heuristic molecular modeling gains an important position in chemistry education since it inherently integrates several conceptual thinking principles. Herein, it is focused on computational analysis of eight potential immunomodulators prepared by Diels-Alder reactions to exemplify con
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Ramasami, Ponnadurai, Hanusha Bhakhoa, and Lydia Rhyman. "Copper(I) Catalyzed [3+2] Cycloaddition Reaction with Mechanistic Disparity: A DFT Study." In The 17th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2013. http://dx.doi.org/10.3390/ecsoc-17-e017.

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Dolzhenko, Anton, Anna Dolzhenko, and Wai-Keung Chui. "Reaction of 2-guanidino-4-quinazolinone with arylaldehydes." In The 10th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2006. http://dx.doi.org/10.3390/ecsoc-10-01382.

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Yamamoto, Hiroki, Takahiro Kozawa, Kazumasa Okamoto, et al. "The reaction mechanism of poly[4-hydroxystyrene-co-4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropyl)-styrene]." In SPIE 31st International Symposium on Advanced Lithography, edited by Qinghuang Lin. SPIE, 2006. http://dx.doi.org/10.1117/12.656262.

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Gong, Shengzhao, Qingsheng Chen, and Mengyi Xu. "Inhibitory Kinetics of 2'-Hydroxy-4'-methoxyacetophenone on Tyrosinase-catalyzing Reaction." In 2015 4th International Conference on Sensors, Measurement and Intelligent Materials. Atlantis Press, 2016. http://dx.doi.org/10.2991/icsmim-15.2016.117.

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Aziz, Azni Abdul, Norhasliza Yusof, Mahirah Idris та Hasan Abu Kassim. "An Improved Reaction Rate Formulation for Charged-Particle Induced Thermonuclear Reaction of [sup 2]H(d,γ)[sup 4]He". У MALAYSIA ANNUAL PHYSICS CONFERENCE 2010 (PERFIK-2010). AIP, 2011. http://dx.doi.org/10.1063/1.3573689.

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Chapuis, Christian, Anna Kucharska, and Janusz Jurczak. "A Comparison of Two Effective Chiral Auxiliaries - (2R)-bornane-10,2-sultam and (2R)-bornane-10,2-cyclohydrazide - using the [4+2] Cycloaddition of Cyclopentadiene to their N,N'-fumaroyl derivatives." In The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01817.

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Baichurin, Ruslan, Vladislav Sergeev, and Sergey Makarenko. "SYNTHESIS OF 4-METHYL-3-NITRO-2-STYRYL-2,3-DIHYDROBENZO[b][1,4]THIAZEPINE BASED ON THE REACTION OF 1-ACETYL1-NITRO-4-PHENYL-1,3-BUTADIENE WITH 2-AMINOTHIOPHENOL." In Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m756.aks-2019/218-219.

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Navarini, Jussara, Helio G. Bonacorso, Carson W. Wiethan, et al. "Synthesis of New 5-Trifluoromethyl-3-alkyl[aryl(heteroaryl)]-4- (2-benzyl-3-hydroxycyclohex-2-enone-2-yl)-1H-pyrazoles by a Ring-Opening Reaction." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0009-1.

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Reports on the topic "[4+2] cycloaddition reaction"

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Iqbal, Sophia. Study of 4He(e, e'p)3H through the (e, e'p) reaction at Q2 = 2(GeV/c)2 and xb = 1.24. Office of Scientific and Technical Information (OSTI), 2013. http://dx.doi.org/10.2172/1133083.

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Führ, Martin, Julian Schenten, and Silke Kleihauer. Integrating "Green Chemistry" into the Regulatory Framework of European Chemicals Policy. Sonderforschungsgruppe Institutionenanalyse, 2019. http://dx.doi.org/10.46850/sofia.9783941627727.

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Abstract:
20 years ago a concept of “Green Chemistry” was formulated by Paul Anastas and John Warner, aiming at an ambitious agenda to “green” chemical products and processes. Today the concept, laid down in a set of 12 principles, has found support in various arenas. This diffusion was supported by enhancements of the legislative framework; not only in the European Union. Nevertheless industry actors – whilst generally supporting the idea – still see “cost and perception remain barriers to green chemistry uptake”. Thus, the questions arise how additional incentives as well as measures to address the ba
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