Artigos de revistas sobre o tema "Diels-Alder cycloaddition reactions"
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Grygorenko, Oleksandr O., Viktoriia S. Moskvina, Oleksandr V. Hryshchuk e Andriy V. Tymtsunik. "Cycloadditions of Alkenylboronic Derivatives". Synthesis 52, n.º 19 (24 de junho de 2020): 2761–80. http://dx.doi.org/10.1055/s-0040-1707159.
Texto completo da fonteBurnell, D. Jean, e Zdenek Valenta. "π-Facial stereoselectivity in the Diels–Alder reactions of a rigid carbocyclic diene: spiro(bicyclo[2.2.1]heptane-2,1′-[2,4]cyclopentadiene)". Canadian Journal of Chemistry 69, n.º 1 (1 de janeiro de 1991): 179–84. http://dx.doi.org/10.1139/v91-028.
Texto completo da fonteSoares, Maria I. L., Ana L. Cardoso e Teresa M. V. D. Pinho e Melo. "Diels–Alder Cycloaddition Reactions in Sustainable Media". Molecules 27, n.º 4 (15 de fevereiro de 2022): 1304. http://dx.doi.org/10.3390/molecules27041304.
Texto completo da fonteZhou, You-Yun, e Christopher Uyeda. "Catalytic reductive [4 + 1]-cycloadditions of vinylidenes and dienes". Science 363, n.º 6429 (21 de fevereiro de 2019): 857–62. http://dx.doi.org/10.1126/science.aau0364.
Texto completo da fonteZezula, Josef, Tomáš Hudlický e Ion Ghiviriga. "Intramolecular Diels-Alder Cycloadditions of cis-Cyclohexadienediols Derived Enzymatically from (2-Azidoethyl)benzene. Construction of Highly Functionalized Bridged Isoquinoline Synthons". Collection of Czechoslovak Chemical Communications 66, n.º 8 (2001): 1269–86. http://dx.doi.org/10.1135/cccc20011269.
Texto completo da fontePratt, Andrew J., Phillip M. Rendle e Peter J. Steel. "Anticancer Prodrug Studies: Diels - Alder Chemistry of 1-Methylthio-1-(p-tolylsulfonyl)ethene". Australian Journal of Chemistry 64, n.º 7 (2011): 945. http://dx.doi.org/10.1071/ch10450.
Texto completo da fonteCarlini, Rina, Kerianne Higgs, Nicholas Taylor e Russell Rodrigo. "Diels–Alder adducts of ortho-benzoquinones: rearrangements and further transformations". Canadian Journal of Chemistry 75, n.º 6 (1 de junho de 1997): 805–16. http://dx.doi.org/10.1139/v97-097.
Texto completo da fonteAyadi, Sameh, e Manef Abderrabba. "Étude DFT des réactions de cycloaddition de type Diels–Alder sur le 4-aza-6-nitrobenzofuroxane". Canadian Journal of Chemistry 85, n.º 5 (1 de maio de 2007): 331–35. http://dx.doi.org/10.1139/v07-026.
Texto completo da fontePiers, Edward, Richard W. Friesen, Paul Kao, Steven J. Rettig e 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, n.º 9 (1 de setembro de 1993): 1463–83. http://dx.doi.org/10.1139/v93-188.
Texto completo da fonteKotha, Sambasivarao, Milind Meshram e Nageswara Panguluri. "Advanced Approaches to Post-Assembly Modification of Peptides by Transition-Metal-Catalyzed Reactions". Synthesis 51, n.º 09 (25 de março de 2019): 1913–22. http://dx.doi.org/10.1055/s-0037-1612418.
Texto completo da fonteCabrera-Trujillo, Jorge Juan, e Israel Fernández. "Understanding exo-selective Diels–Alder reactions involving Fischer-type carbene complexes". Organic & Biomolecular Chemistry 17, n.º 11 (2019): 2985–91. http://dx.doi.org/10.1039/c9ob00132h.
Texto completo da fonteFallis, Alex G. "1998 Alfred Bader Award Lecture Tangents and targets: The synthetic highway from natural products to medicine". Canadian Journal of Chemistry 77, n.º 2 (1 de fevereiro de 1999): 159–77. http://dx.doi.org/10.1139/v98-233.
Texto completo da fonteCantín, Ángel, M. Victoria Gomez e Antonio de la Hoz. "Diels–Alder reactions in confined spaces: the influence of catalyst structure and the nature of active sites for the retro-Diels–Alder reaction". Beilstein Journal of Organic Chemistry 12 (13 de outubro de 2016): 2181–88. http://dx.doi.org/10.3762/bjoc.12.208.
Texto completo da fonteAronica, Laura, e Gianluigi Albano. "Cyclization Reactions for the Synthesis of Phthalans and Isoindolines". Synthesis 50, n.º 06 (31 de janeiro de 2018): 1209–27. http://dx.doi.org/10.1055/s-0037-1609175.
Texto completo da fonteSu, Zhishan, e Chan Kyung Kim. "Trienamine catalysis for asymmetric Diels–Alder reactions of 2,4-dienones: a theoretical investigation". Organic & Biomolecular Chemistry 13, n.º 22 (2015): 6313–24. http://dx.doi.org/10.1039/c5ob00797f.
Texto completo da fonteEscalante, Carlos H., Eder I. Martínez-Mora, Carlos Espinoza-Hicks, Alejandro A. Camacho-Dávila, Fernando R. Ramos-Morales, Francisco Delgado e Joaquín Tamariz. "Highly selective Diels–Alder and Heck arylation reactions in a divergent synthesis of isoindolo- and pyrrolo-fused polycyclic indoles from 2-formylpyrrole". Beilstein Journal of Organic Chemistry 16 (17 de junho de 2020): 1320–34. http://dx.doi.org/10.3762/bjoc.16.113.
Texto completo da fonteYang, Zhongyue, Song Yang, Peiyuan Yu, Yanwei Li, Charles Doubleday, Jiyong Park, Ashay Patel et al. "Influence of water and enzyme SpnF on the dynamics and energetics of the ambimodal [6+4]/[4+2] cycloaddition". Proceedings of the National Academy of Sciences 115, n.º 5 (18 de janeiro de 2018): E848—E855. http://dx.doi.org/10.1073/pnas.1719368115.
Texto completo da fonteBreton, Gary W., e Kenneth L. Martin. "Exploring the Limits of Reactivity of N-Methyl-1,2,4-triazoline-3,5-dione (MeTAD) with Disubstituted Bicycloalkadienes in the Homo-Diels–Alder Reaction". Organics 4, n.º 1 (31 de dezembro de 2022): 41–48. http://dx.doi.org/10.3390/org4010002.
Texto completo da fonteFulton, Brandon B., Alexia J. Hartzell, H. V. Rasika Dias e Carl J. Lovely. "Room Temperature Diels–Alder Reactions of 4-Vinylimidazoles". Molecules 29, n.º 8 (22 de abril de 2024): 1902. http://dx.doi.org/10.3390/molecules29081902.
Texto completo da fonteRao, Nagaraj. "ASYMMETRIC ORGANOCATALYSIS". INDIAN DRUGS 58, n.º 10 (16 de dezembro de 2021): 5–6. http://dx.doi.org/10.53879/id.58.10.p0005.
Texto completo da fonteTejero, Alvaro G., María Carmona, Ricardo Rodríguez, Fernando Viguri, Fernando J. Lahoz, Pilar García-Orduña e Daniel Carmona. "Synthesis of chiral-at-metal rhodium complexes from achiral tripodal tetradentate ligands: resolution and application to enantioselective Diels–Alder and 1,3-dipolar cycloadditions". RSC Advances 12, n.º 53 (2022): 34704–14. http://dx.doi.org/10.1039/d2ra06982b.
Texto completo da fonteCharlton, James L., Guy L. Plourde e Glenn H. Penner. "Asymmetric induction in Diels–Alder reactions of α-alkoxyorthoquinodimethanes". Canadian Journal of Chemistry 67, n.º 6 (1 de junho de 1989): 1010–14. http://dx.doi.org/10.1139/v89-153.
Texto completo da fonteWilliams, C. Luke, Katherine P. Vinter, Chun-Chih Chang, Ruichang Xiong, Sara K. Green, Stanley I. Sandler, Dionisios G. Vlachos, Wei Fan e Paul J. Dauenhauer. "Kinetic regimes in the tandem reactions of H-BEA catalyzed formation of p-xylene from dimethylfuran". Catalysis Science & Technology 6, n.º 1 (2016): 178–87. http://dx.doi.org/10.1039/c5cy01320h.
Texto completo da fonteBădoiu, Andrei, Yasmin Brinkmann, Florian Viton e E. Peter Kündig. "Asymmetric Lewis acid-catalyzed 1,3-dipolar cycloadditions". Pure and Applied Chemistry 80, n.º 5 (1 de janeiro de 2008): 1013–18. http://dx.doi.org/10.1351/pac200880051013.
Texto completo da fonteDuret, Guillaume, Vincent Le Fouler, Philippe Bisseret, Vincent Bizet e Nicolas Blanchard. "Diels-Alder and Formal Diels-Alder Cycloaddition Reactions of Ynamines and Ynamides". European Journal of Organic Chemistry 2017, n.º 46 (8 de setembro de 2017): 6816–30. http://dx.doi.org/10.1002/ejoc.201700986.
Texto completo da fonteBoger, Dale L., e Christine E. Brotherton. "Diels-alder cycloaddition reactions of cyclopropenone ketals". Tetrahedron 42, n.º 11 (janeiro de 1986): 2777–85. http://dx.doi.org/10.1016/s0040-4020(01)90567-8.
Texto completo da fonteLaurent, Alain, Nidia P. Villalva-Servín, Pat Forgione, Peter D. Wilson, David V. Smil e Alex G. Fallis. "Part 1: Efficient strategies for the construction of variably substituted bicyclo[5.3.1]undecenones (AB taxane ring systems)". Canadian Journal of Chemistry 82, n.º 2 (1 de fevereiro de 2004): 215–26. http://dx.doi.org/10.1139/v03-200.
Texto completo da fonteTomé, Augusto C., Maria G. P. M. S. Neves e José A. S. Cavaleiro. "Porphyrins and other pyrrolic macrocycles in cycloaddition reactions". Journal of Porphyrins and Phthalocyanines 13, n.º 04n05 (abril de 2009): 408–14. http://dx.doi.org/10.1142/s1088424609000619.
Texto completo da fonteHou, Ji-Qin, Jiang-Hong Yu, Heng Zhao, Ying-Ying Dong, Qiu-Shi Peng, Bao-Bao Zhang e Hao Wang. "Biomimetic total syntheses of baefrutones A–D, baeckenon B, and frutescones A, D–F". Organic & Biomolecular Chemistry 18, n.º 6 (2020): 1135–39. http://dx.doi.org/10.1039/c9ob02490e.
Texto completo da fonteBednarek, Melania, e Przemysław Kubisa. "Reversible networks of degradable polyesters containing weak covalent bonds". Polymer Chemistry 10, n.º 15 (2019): 1848–72. http://dx.doi.org/10.1039/c8py01731j.
Texto completo da fonteBauer, John B., Fatima Diab, Cäcilia Maichle-Mössmer, Hartmut Schubert e Holger F. Bettinger. "Synthesis of the [11]Cyclacene Framework by Repetitive Diels–Alder Cycloadditions". Molecules 26, n.º 10 (20 de maio de 2021): 3047. http://dx.doi.org/10.3390/molecules26103047.
Texto completo da fontePetko, Dina, Matthew Stratton e William Tam. "Ruthenium-catalyzed Bis-Homo-Diels-Alder reaction: searching for commercially available catalysts and expanding the scope of reaction". Canadian Journal of Chemistry 96, n.º 12 (dezembro de 2018): 1115–21. http://dx.doi.org/10.1139/cjc-2018-0117.
Texto completo da fonteHamzehloueian, Mahshid, Saeid Yeganegi, Yaghoub Sarrafi, Kamal Alimohammadi e Marzieh Sadatshahabi. "A theoretical investigation on the regioselectivity of the intramolecular hetero Diels-Alder and 1,3-dipolar cycloaddition of 2-vinyloxybenzaldehyde derivatives". Journal of the Serbian Chemical Society 79, n.º 8 (2014): 911–24. http://dx.doi.org/10.2298/jsc140121012h.
Texto completo da fonteJursic, Branko S. "AM1 semiempirical study of benzopyrroles as dienes for Diels-Alder reaction". Canadian Journal of Chemistry 74, n.º 1 (1 de janeiro de 1996): 114–20. http://dx.doi.org/10.1139/v96-015.
Texto completo da fonteBrossard, Dominique, Pascal Retailleau, Vincent Dumontet, Philippe Breton, Sandy Desrat e Fanny Roussi. "Fast & easy preparation of 3D scaffolds from methyl benzoate by a diversity oriented synthesis strategy based on Diels–Alder and ene-reactions". Organic & Biomolecular Chemistry 15, n.º 26 (2017): 5585–92. http://dx.doi.org/10.1039/c7ob01236e.
Texto completo da fonteKoçak, Ramazan, e Arif Daştan. "Synthesis of dibenzosuberenone-based novel polycyclic π-conjugated dihydropyridazines, pyridazines and pyrroles". Beilstein Journal of Organic Chemistry 17 (15 de março de 2021): 719–29. http://dx.doi.org/10.3762/bjoc.17.61.
Texto completo da fonteGribble, G. W. "Novel chemistry of indole in the synthesis of heterocycles". Pure and Applied Chemistry 75, n.º 10 (1 de janeiro de 2003): 1417–32. http://dx.doi.org/10.1351/pac200375101417.
Texto completo da fonteÇapan, İrfan, e Süleyman Servi. "Synthesis of New C2-Symmetric Chiral Benzimidazole Derivatives Having Norbornene/Dibenzobarrelene Skeletons". Letters in Organic Chemistry 17, n.º 10 (17 de novembro de 2020): 801–5. http://dx.doi.org/10.2174/1570178616666190731105327.
Texto completo da fonteMlostoń, Grzegorz, Yuriy Shermolovich e Heinz Heimgartner. "Synthesis of Fluorinated and Fluoroalkylated Heterocycles Containing at Least One Sulfur Atom via Cycloaddition Reactions". Materials 15, n.º 20 (17 de outubro de 2022): 7244. http://dx.doi.org/10.3390/ma15207244.
Texto completo da fonteKorol, Nataliya, Mikhailo Slivka e Oksana Holovko-Kamoshenkova. "Cycloaddition reactions of 4-phenyl-3H-1,2,4-triazole-3,5(4H)-dione (PTAD) and 4-methyl-3H-1,2,4-triazole-3,5(4H)-dione (MTAD): A short review". Organic Communications 13, n.º 4 (26 de dezembro de 2020): 146–54. http://dx.doi.org/10.25135/acg.oc.88.20.11.1870.
Texto completo da fonteBeck, Janina, Olaf Fuhr, Martin Nieger e Stefan Bräse. "A versatile Diels–Alder approach to functionalized hydroanthraquinones". Royal Society Open Science 7, n.º 11 (novembro de 2020): 200626. http://dx.doi.org/10.1098/rsos.200626.
Texto completo da fonteSpino, Claude, e Jason Crawford. "2-Carbomethoxy-1,3-butadiene: an electronically activated diene in [4 + 2] cycloadditions with electron-deficient dienophiles". Canadian Journal of Chemistry 71, n.º 7 (1 de julho de 1993): 1094–97. http://dx.doi.org/10.1139/v93-145.
Texto completo da fonteBates, Robert W., Andrew J. Pratt, Phillip M. Rendle e Ward T. Robinson. "Diels - Alder Reactions of 1,1-Bis(methylthio)ethene with Pyran-2-ones." Australian Journal of Chemistry 51, n.º 5 (1998): 383. http://dx.doi.org/10.1071/c97128.
Texto completo da fonteMoore, Jonathan C., E. Stephen Davies, Darren A. Walsh, Pallavi Sharma e John E. Moses. "Formal synthesis of kingianin A based upon a novel electrochemically-induced radical cation Diels–Alder reaction". Chem. Commun. 50, n.º 83 (2014): 12523–25. http://dx.doi.org/10.1039/c4cc05906a.
Texto completo da fontede Sousa, Andrea L. F., José E. P. Cardoso Filho, Blanka Wladislaw, Liliana Marzorati e Claudio Di Vitta. "Studies on chemo- and diastereo-selectivity of the Diels–Alder reactions of sulfinyltoluquinones with cyclopentadiene". Canadian Journal of Chemistry 87, n.º 8 (agosto de 2009): 1135–43. http://dx.doi.org/10.1139/v09-070.
Texto completo da fonteCharlton, James L., e Shawn Maddaford. "The mechanism of stereoselectivity in the cycloaddition reactions of α-hydroxy-ortho-quinodimethanes with the fumarate of methyl lactate and mandelate". Canadian Journal of Chemistry 71, n.º 6 (1 de junho de 1993): 827–33. http://dx.doi.org/10.1139/v93-110.
Texto completo da fonteZeller, Matthias, Allen D. Hunter, Paul Sampson e Nataliya Chumachenko. "1-[(E)-Butadienylsulfonyl]-3,3-dimethylbut-2-yl methacrylate". Acta Crystallographica Section E Structure Reports Online 62, n.º 4 (15 de março de 2006): o1369—o1370. http://dx.doi.org/10.1107/s1600536806008014.
Texto completo da fonteGillard, James R., Michael J. Newlands, John N. Bridson e D. Jean Burnell. "π-Facial stereoselectivity in the Diels–Alder reactions of benzene oxides". Canadian Journal of Chemistry 69, n.º 9 (1 de setembro de 1991): 1337–43. http://dx.doi.org/10.1139/v91-199.
Texto completo da fonteJasiński, Radomir. "On the Question of Stepwise [4+2] Cycloaddition Reactions and Their Stereochemical Aspects". Symmetry 13, n.º 10 (11 de outubro de 2021): 1911. http://dx.doi.org/10.3390/sym13101911.
Texto completo da fonteWard, Dale E., Thomas E. Nixey, Yuanzhu Gai, Matthew J. Hrapchak e M. Saeed Abaee. "Intramolecular Diels–Alder reactions of 2H-thiopyran dienes". Canadian Journal of Chemistry 74, n.º 7 (1 de julho de 1996): 1418–36. http://dx.doi.org/10.1139/v96-160.
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