Статті в журналах з теми "Dienophiles"
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Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Dienophiles".
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Talma, A. G., R. N. Datta, and J. Aerts. "Quantum Mechanical Calculations to Assess the Antireversion Effects of Several Dienophiles." Rubber Chemistry and Technology 74, no. 4 (September 1, 2001): 574–82. http://dx.doi.org/10.5254/1.3544958.
Повний текст джерелаOmar, Yasser M., Giulia Santucci, and Kamyar Afarinkia. "tert-Butyl(2-oxo-2H-pyran-5-yl)carbamate as the First Chameleon Diene Bearing an Electron-Donating Substituent." Molecules 27, no. 17 (September 2, 2022): 5666. http://dx.doi.org/10.3390/molecules27175666.
Повний текст джерелаSu, Zhishan, and Chan Kyung Kim. "Trienamine catalysis for asymmetric Diels–Alder reactions of 2,4-dienones: a theoretical investigation." Organic & Biomolecular Chemistry 13, no. 22 (2015): 6313–24. http://dx.doi.org/10.1039/c5ob00797f.
Повний текст джерелаSeo, Jeong-Min, and Jong-Beom Baek. "A solvent-free Diels–Alder reaction of graphite into functionalized graphene nanosheets." Chem. Commun. 50, no. 93 (2014): 14651–53. http://dx.doi.org/10.1039/c4cc07173e.
Повний текст джерелаWard, Dale E., Thomas E. Nixey, Yuanzhu Gai, Matthew J. Hrapchak, and M. Saeed Abaee. "Intramolecular Diels–Alder reactions of 2H-thiopyran dienes." Canadian Journal of Chemistry 74, no. 7 (July 1, 1996): 1418–36. http://dx.doi.org/10.1139/v96-160.
Повний текст джерелаLiu, Hsing-Jang, Dan-Xiong Wang, Jeung Bea Kim, Eric N. C. Browne, and Yu Wang. "Activated cyclooctenones are effective dienophiles." Canadian Journal of Chemistry 75, no. 6 (June 1, 1997): 899–912. http://dx.doi.org/10.1139/v97-108.
Повний текст джерелаLiu, Zhang, Wang, Zan, and Zhang. "The Role of Iodine Catalyst in the Synthesis of 22-Carbon Tricarboxylic Acid and Its Ester: A Case Study." Catalysts 9, no. 12 (November 20, 2019): 972. http://dx.doi.org/10.3390/catal9120972.
Повний текст джерелаNdibwami, Alexis, Serge Lamothe, Daniel Guay, Raymond Plante, Pierre Soucy, Solo Goldstein, and Pierre Deslongchamps. "Transannular Diels–Alder reactions on 14-membered macrocyclic trienes. Part I: stereoselective syntheses of the macrocyclic trienes precursors." Canadian Journal of Chemistry 71, no. 5 (May 1, 1993): 695–713. http://dx.doi.org/10.1139/v93-094.
Повний текст джерелаBarta, Petra, Ferenc Fülöp, and István Szatmári. "Mannich base-connected syntheses mediated by ortho-quinone methides." Beilstein Journal of Organic Chemistry 14 (March 6, 2018): 560–75. http://dx.doi.org/10.3762/bjoc.14.43.
Повний текст джерелаThiessen, Merlina, and Volker Abetz. "Influence of the Glass Transition Temperature and the Density of Crosslinking Groups on the Reversibility of Diels-Alder Polymer Networks." Polymers 13, no. 8 (April 7, 2021): 1189. http://dx.doi.org/10.3390/polym13081189.
Повний текст джерелаLaue, Jörg, Gunther Seitz та Hans Waßmuth. "Synthese und [4+2]-Cycloadditionen von 4a, 8a-Methanophthalazin, das erste Propellan mit einem elektronenreichen und einem elektronenarmen 4π-Diensystem/Synthesis and [4+2] Cycloaddition Reactions of 4a, 8a-Methanophthalazine, the First Propellane with an Electronrich and an Electrondeficient 4π-Diene System". Zeitschrift für Naturforschung B 51, № 3 (1 березня 1996): 348–58. http://dx.doi.org/10.1515/znb-1996-0309.
Повний текст джерелаBeig, Nosheen, Aarti Peswani, and Raj Kumar Bansal. "Dienophilic reactivity of 2-phosphaindolizines: a conceptual DFT investigation." Beilstein Journal of Organic Chemistry 18 (September 13, 2022): 1217–24. http://dx.doi.org/10.3762/bjoc.18.127.
Повний текст джерелаKurpanik, Aneta, Marek Matussek, Piotr Lodowski, Grażyna Szafraniec-Gorol, Michał Krompiec, and Stanisław Krompiec. "Diels–Alder Cycloaddition to the Bay Region of Perylene and Its Derivatives as an Attractive Strategy for PAH Core Expansion: Theoretical and Practical Aspects." Molecules 25, no. 22 (November 17, 2020): 5373. http://dx.doi.org/10.3390/molecules25225373.
Повний текст джерелаMa, Zhiyuan, Feng Ni, Grace H. C. Woo, Sie-Mun Lo, Philip M. Roveto, Scott E. Schaus та John K. Snyder. "An intramolecular inverse electron demand Diels–Alder approach to annulated α-carbolines". Beilstein Journal of Organic Chemistry 8 (6 червня 2012): 829–40. http://dx.doi.org/10.3762/bjoc.8.93.
Повний текст джерелаWelker, Mark E. "Boron and Silicon-Substituted 1,3-Dienes and Dienophiles and Their Use in Diels-Alder Reactions." Molecules 25, no. 16 (August 16, 2020): 3740. http://dx.doi.org/10.3390/molecules25163740.
Повний текст джерелаWei, Hong Liang, Ya Li Feng, Hui Juan Chu, and Kai Yao. "Fabrication of Supramolecular Structured Hydrogels Based on Diels-Alder Click Reaction." Advanced Materials Research 562-564 (August 2012): 405–8. http://dx.doi.org/10.4028/www.scientific.net/amr.562-564.405.
Повний текст джерелаWard, Dale E., and Yuanzhu Gai. "Lewis acid mediated Diels–Alder reactions of 2H-thiopyrans." Canadian Journal of Chemistry 70, no. 10 (October 1, 1992): 2627–34. http://dx.doi.org/10.1139/v92-331.
Повний текст джерелаPiers, Edward, Richard W. Friesen, Paul Kao, Steven J. Rettig, and James Trotter. "Synthesis of functionalized hexahydro-, octahydro-, and decahydro-1H-phenalenes via Diels–Alder reactions of 1-methylene-4a-methoxycarbonyl-1,2,3,4,4a,5,6,7-octahydronaphthalene and related dienes." Canadian Journal of Chemistry 71, no. 9 (September 1, 1993): 1463–83. http://dx.doi.org/10.1139/v93-188.
Повний текст джерелаAyadi, Sameh, and Manef Abderrabba. "Étude DFT des réactions de cycloaddition de type Diels–Alder sur le 4-aza-6-nitrobenzofuroxane." Canadian Journal of Chemistry 85, no. 5 (May 1, 2007): 331–35. http://dx.doi.org/10.1139/v07-026.
Повний текст джерелаLiang, Zhiling, Houhe Liu, Nianjun Su, Dandan Song, Yun Zhang, Hong Huang, Jianqi Zheng, Cheng Zhong, and Guodong Ye. "Study of the Deformation/Interaction Model: How Interactions Increase the Reaction Barrier." Journal of Chemistry 2018 (2018): 1–8. http://dx.doi.org/10.1155/2018/3106297.
Повний текст джерелаSultan, Mujeeb A., Mansour S. A. Galil, Mohyeddine Al-Qubati, Mufeed M. Omar, and Assem Barakat. "Synthesis, Molecular Docking, Druglikeness Analysis, and ADMET Prediction of the Chlorinated Ethanoanthracene Derivatives as Possible Antidepressant Agents." Applied Sciences 10, no. 21 (October 31, 2020): 7727. http://dx.doi.org/10.3390/app10217727.
Повний текст джерелаRogers, Christine, and Brian A. Keay. "The effect of Lewis acids on the intramolecular Diels–Alder reaction of the furan diene." Canadian Journal of Chemistry 70, no. 12 (December 1, 1992): 2929–47. http://dx.doi.org/10.1139/v92-375.
Повний текст джерелаLee, Jennifer J., and George A. Kraus. "One-pot formal synthesis of biorenewable terephthalic acid from methyl coumalate and methyl pyruvate." Green Chem. 16, no. 4 (2014): 2111–16. http://dx.doi.org/10.1039/c3gc42487a.
Повний текст джерелаBorisevich, Sophia S., Alena V. Kovalskaya, Inna P. Tsypysheva, and Sergey L. Khursan. "Thermodynamically controlled Diels–Alder reaction of 12-N-methylcytisine: A DFT study." Journal of Theoretical and Computational Chemistry 13, no. 06 (September 2014): 1450048. http://dx.doi.org/10.1142/s0219633614500485.
Повний текст джерелаRogers, Christine, and Brian A. Keay. "Diastereoselective intramolecular Diels–Alder reactions of the furan diene: the synthesis of (±)-1,4-epoxycadinane." Canadian Journal of Chemistry 71, no. 5 (May 1, 1993): 611–22. http://dx.doi.org/10.1139/v93-081.
Повний текст джерелаParedes, Elisa, Betina Biolatto, Marı́a Kneeteman, and Pedro M. Mancini. "Nitronaphthalenes as Diels–Alder dienophiles." Tetrahedron Letters 41, no. 42 (October 2000): 8079–82. http://dx.doi.org/10.1016/s0040-4039(00)01436-2.
Повний текст джерелаAdam, Waldemar, Metin Balci, Zeynep Ceylan, and Ricardo Francisco Hinz. "Reactions of Benzocycloheptenes with Dienophiles." Chemische Berichte 124, no. 2 (February 1991): 383–86. http://dx.doi.org/10.1002/cber.19911240222.
Повний текст джерелаWard, Dale E., Yuanzhu Gai, and Wajdi M. Zoghaib. "Diels–Alder reactions of activated 2H-thiopyrans." Canadian Journal of Chemistry 69, no. 10 (October 1, 1991): 1487–97. http://dx.doi.org/10.1139/v91-220.
Повний текст джерелаBornadiego, Ana, Jesús Díaz, and Carlos F. Marcos. "Tandem synthesis of 4-aminoxanthones is controlled by a water-assisted tautomerization: a general straightforward reaction." Organic & Biomolecular Chemistry 17, no. 6 (2019): 1410–22. http://dx.doi.org/10.1039/c8ob02527d.
Повний текст джерелаAbbasov, Mikail E., Brandi M. Hudson, Weixu Kong, Dean J. Tantillo, and Daniel Romo. "Enantioselective Diels-Alder-lactamization organocascades employing a furan-based diene." Organic & Biomolecular Chemistry 15, no. 15 (2017): 3179–83. http://dx.doi.org/10.1039/c6ob02738e.
Повний текст джерелаLording, William J., Thomas Fallon, Michael S. Sherburn, and Michael N. Paddon-Row. "The simplest Diels–Alder reactions are not endo-selective." Chemical Science 11, no. 43 (2020): 11915–26. http://dx.doi.org/10.1039/d0sc04553e.
Повний текст джерелаBillaud, Emilie M. F., Elnaz Shahbazali, Muneer Ahamed, Frederik Cleeren, Timothy Noël, Michel Koole, Alfons Verbruggen, Volker Hessel, and Guy Bormans. "Micro-flow photosynthesis of new dienophiles for inverse-electron-demand Diels–Alder reactions. Potential applications for pretargeted in vivo PET imaging." Chemical Science 8, no. 2 (2017): 1251–58. http://dx.doi.org/10.1039/c6sc02933g.
Повний текст джерелаHuang, Ci-Jhang, and Elise Y. Li. "Molecular design principles towards exo-exclusive Diels–Alder reactions." RSC Advances 9, no. 13 (2019): 7246–50. http://dx.doi.org/10.1039/c8ra10438g.
Повний текст джерелаKaur, Jasneet, Pankaj Chauhan та Swapandeep Singh Chimni. "α,α-Dicyanoolefins: versatile substrates in organocatalytic asymmetric transformations". Organic & Biomolecular Chemistry 14, № 33 (2016): 7832–47. http://dx.doi.org/10.1039/c6ob01229a.
Повний текст джерелаZhu, Jun, Stephen Li, Carmen Wängler, Björn Wängler, R. Bruce Lennox, and Ralf Schirrmacher. "Synthesis of 3-chloro-6-((4-(di-tert-butyl[18F]fluorosilyl)-benzyl)oxy)-1,2,4,5-tetrazine ([18F]SiFA-OTz) for rapid tetrazine-based18F-radiolabeling." Chemical Communications 51, no. 62 (2015): 12415–18. http://dx.doi.org/10.1039/c5cc03623b.
Повний текст джерелаAbbasov, Mikail E., Brandi M. Hudson, Dean J. Tantillo та Daniel Romo. "Stereodivergent, Diels–Alder-initiated organocascades employing α,β-unsaturated acylammonium salts: scope, mechanism, and application". Chemical Science 8, № 2 (2017): 1511–24. http://dx.doi.org/10.1039/c6sc04273b.
Повний текст джерелаKoner, Abhishek, Bulat M. Gabidullin, Zsolt Kelemen, László Nyulászi, Georgii I. Nikonov, and Rainer Streubel. "7-Metalla-1,4-diphosphanorbornadienes: cycloaddition of monovalent group 13 NacNac complexes to a stable 1,4-diphosphinine." Dalton Transactions 48, no. 23 (2019): 8248–53. http://dx.doi.org/10.1039/c9dt01425j.
Повний текст джерелаItoh, Takashi, Akio Ohsawa, Mamiko Okada, Terumitsu Kaihoh, and Hiroshi Igeta. "Reaction of 1,2,3-triazine with dienophiles." CHEMICAL & PHARMACEUTICAL BULLETIN 33, no. 7 (1985): 3050–52. http://dx.doi.org/10.1248/cpb.33.3050.
Повний текст джерелаWilliams, D. R., and R. D. Gaston. "Intramolecular cycloadditions using vinyl sulfide dienophiles." Tetrahedron Letters 27, no. 13 (January 1986): 1485–88. http://dx.doi.org/10.1016/s0040-4039(00)84291-4.
Повний текст джерелаBlades, Kevin, Thierry P. Lequeux, and Jonathan M. Percy. "Reactive dienophiles containing a difluoromethylenephosphonato group." Chemical Communications, no. 12 (1996): 1457. http://dx.doi.org/10.1039/cc9960001457.
Повний текст джерелаRiviere, Pierre, Antony Mauvais, and Ekkehard Winterfeldt. "Pure enantiomers from simple, symmetric dienophiles." Tetrahedron: Asymmetry 5, no. 9 (September 1994): 1831–46. http://dx.doi.org/10.1016/0957-4166(94)80092-8.
Повний текст джерелаDavis, Anna E., Jared M. Lowe, and Michael K. Hilinski. "Vinylazaarenes as dienophiles in Lewis acid-promoted Diels–Alder reactions." Chemical Science 12, no. 48 (2021): 15947–52. http://dx.doi.org/10.1039/d1sc05095h.
Повний текст джерелаFerreira, Juliana, Vera C. M. Duarte, Jennifer Noro, António Gil Fortes та Maria J. Alves. "Total facial selectivity of a d-erythrosyl aromatic imine in [4π + 2π] cycloadditions; synthesis of 2-alkylpolyol 1,2,3,4-tetrahydroquinolines". Organic & Biomolecular Chemistry 14, № 10 (2016): 2930–37. http://dx.doi.org/10.1039/c5ob02594j.
Повний текст джерелаShimizu, Makoto, Toshihiro Yamamoto, Hiroaki Shindo, Isao Mizota, and Yusong Zhu. "2,3-Dimethoxy-2,3-dimethyl-1,4-dioxane as a useful precursor to 2,3-dimethylene-1,4-dioxane for [4+2] cycloaddition reaction." RSC Advances 11, no. 14 (2021): 7972–80. http://dx.doi.org/10.1039/d1ra00329a.
Повний текст джерелаYamada, S., K. Hondo, T. Konno, and T. Ishihara. "Concise preparation of fluorine-containing carbocycles involving the Diels–Alder reaction using fluorinated alkene or diene derivatives." RSC Advances 6, no. 34 (2016): 28458–69. http://dx.doi.org/10.1039/c6ra00569a.
Повний текст джерелаAmeta, Sandeep, Juliane Becker, and Andres Jäschke. "RNA–peptide conjugate synthesis by inverse-electron demand Diels–Alder reaction." Org. Biomol. Chem. 12, no. 26 (2014): 4701–7. http://dx.doi.org/10.1039/c4ob00076e.
Повний текст джерелаSchnierle, Marc, Svenja Blickle, Vasileios Filippou, and Mark R. Ringenberg. "Tetrazine metallation boosts rate and regioselectivity of inverse electron demand Diels–Alder (iEDDA) addition of dienophiles." Chemical Communications 56, no. 80 (2020): 12033–36. http://dx.doi.org/10.1039/d0cc03805a.
Повний текст джерелаLanglois, Yves. "New Uses of Oxazolines, Oxazoline N-Oxides and Dioxolanyliums in Asymmetric Synthesis." Current Organic Chemistry 2, no. 1 (January 1998): 1–18. http://dx.doi.org/10.2174/1385272802666220126210228.
Повний текст джерелаKvyatkovskaya, Elizaveta A., Polina P. Epifanova, Eugeniya V. Nikitina, Aleksey A. Senin, Victor N. Khrustalev, Kirill B. Polyanskii, and Fedor I. Zubkov. "Synthesis and ethylene-promoted metathesis of adducts of tandem [4+2]/[4+2] cycloaddition between bis-furyl dienes and maleic acid derivatives." New Journal of Chemistry 45, no. 7 (2021): 3400–3407. http://dx.doi.org/10.1039/d0nj04528d.
Повний текст джерелаBegum, Imtiaz, Tim Kalisch, Gregor Schnakenburg, Zsolt Kelemen, László Nyulászi, and Rainer Streubel. "[4 + 2]-Cycloadditions of a thiazol-based tricyclic 1,4-diphosphinine and a new easy 1,4-diphosphinine protection deprotection strategy." Dalton Transactions 49, no. 36 (2020): 12776–79. http://dx.doi.org/10.1039/d0dt02529a.
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