Articoli di riviste sul 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. 19 (24 giugno 2020): 2761–80. http://dx.doi.org/10.1055/s-0040-1707159.
Testo completoBurnell, 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. 1 (1 gennaio 1991): 179–84. http://dx.doi.org/10.1139/v91-028.
Testo completoSoares, Maria I. L., Ana L. Cardoso e Teresa M. V. D. Pinho e Melo. "Diels–Alder Cycloaddition Reactions in Sustainable Media". Molecules 27, n. 4 (15 febbraio 2022): 1304. http://dx.doi.org/10.3390/molecules27041304.
Testo completoZhou, You-Yun, e Christopher Uyeda. "Catalytic reductive [4 + 1]-cycloadditions of vinylidenes and dienes". Science 363, n. 6429 (21 febbraio 2019): 857–62. http://dx.doi.org/10.1126/science.aau0364.
Testo completoZezula, 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. 8 (2001): 1269–86. http://dx.doi.org/10.1135/cccc20011269.
Testo completoPratt, 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. 7 (2011): 945. http://dx.doi.org/10.1071/ch10450.
Testo completoCarlini, Rina, Kerianne Higgs, Nicholas Taylor e Russell Rodrigo. "Diels–Alder adducts of ortho-benzoquinones: rearrangements and further transformations". Canadian Journal of Chemistry 75, n. 6 (1 giugno 1997): 805–16. http://dx.doi.org/10.1139/v97-097.
Testo completoAyadi, 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. 5 (1 maggio 2007): 331–35. http://dx.doi.org/10.1139/v07-026.
Testo completoPiers, 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. 9 (1 settembre 1993): 1463–83. http://dx.doi.org/10.1139/v93-188.
Testo completoKotha, Sambasivarao, Milind Meshram e Nageswara Panguluri. "Advanced Approaches to Post-Assembly Modification of Peptides by Transition-Metal-Catalyzed Reactions". Synthesis 51, n. 09 (25 marzo 2019): 1913–22. http://dx.doi.org/10.1055/s-0037-1612418.
Testo completoCabrera-Trujillo, Jorge Juan, e Israel Fernández. "Understanding exo-selective Diels–Alder reactions involving Fischer-type carbene complexes". Organic & Biomolecular Chemistry 17, n. 11 (2019): 2985–91. http://dx.doi.org/10.1039/c9ob00132h.
Testo completoFallis, Alex G. "1998 Alfred Bader Award Lecture Tangents and targets: The synthetic highway from natural products to medicine". Canadian Journal of Chemistry 77, n. 2 (1 febbraio 1999): 159–77. http://dx.doi.org/10.1139/v98-233.
Testo completoCantín, 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 ottobre 2016): 2181–88. http://dx.doi.org/10.3762/bjoc.12.208.
Testo completoAronica, Laura, e Gianluigi Albano. "Cyclization Reactions for the Synthesis of Phthalans and Isoindolines". Synthesis 50, n. 06 (31 gennaio 2018): 1209–27. http://dx.doi.org/10.1055/s-0037-1609175.
Testo completoSu, Zhishan, e Chan Kyung Kim. "Trienamine catalysis for asymmetric Diels–Alder reactions of 2,4-dienones: a theoretical investigation". Organic & Biomolecular Chemistry 13, n. 22 (2015): 6313–24. http://dx.doi.org/10.1039/c5ob00797f.
Testo completoEscalante, 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 giugno 2020): 1320–34. http://dx.doi.org/10.3762/bjoc.16.113.
Testo completoYang, 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. 5 (18 gennaio 2018): E848—E855. http://dx.doi.org/10.1073/pnas.1719368115.
Testo completoBreton, 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. 1 (31 dicembre 2022): 41–48. http://dx.doi.org/10.3390/org4010002.
Testo completoFulton, Brandon B., Alexia J. Hartzell, H. V. Rasika Dias e Carl J. Lovely. "Room Temperature Diels–Alder Reactions of 4-Vinylimidazoles". Molecules 29, n. 8 (22 aprile 2024): 1902. http://dx.doi.org/10.3390/molecules29081902.
Testo completoRao, Nagaraj. "ASYMMETRIC ORGANOCATALYSIS". INDIAN DRUGS 58, n. 10 (16 dicembre 2021): 5–6. http://dx.doi.org/10.53879/id.58.10.p0005.
Testo completoTejero, 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. 53 (2022): 34704–14. http://dx.doi.org/10.1039/d2ra06982b.
Testo completoCharlton, James L., Guy L. Plourde e Glenn H. Penner. "Asymmetric induction in Diels–Alder reactions of α-alkoxyorthoquinodimethanes". Canadian Journal of Chemistry 67, n. 6 (1 giugno 1989): 1010–14. http://dx.doi.org/10.1139/v89-153.
Testo completoWilliams, 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. 1 (2016): 178–87. http://dx.doi.org/10.1039/c5cy01320h.
Testo completoBădoiu, Andrei, Yasmin Brinkmann, Florian Viton e E. Peter Kündig. "Asymmetric Lewis acid-catalyzed 1,3-dipolar cycloadditions". Pure and Applied Chemistry 80, n. 5 (1 gennaio 2008): 1013–18. http://dx.doi.org/10.1351/pac200880051013.
Testo completoDuret, 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. 46 (8 settembre 2017): 6816–30. http://dx.doi.org/10.1002/ejoc.201700986.
Testo completoBoger, Dale L., e Christine E. Brotherton. "Diels-alder cycloaddition reactions of cyclopropenone ketals". Tetrahedron 42, n. 11 (gennaio 1986): 2777–85. http://dx.doi.org/10.1016/s0040-4020(01)90567-8.
Testo completoLaurent, 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. 2 (1 febbraio 2004): 215–26. http://dx.doi.org/10.1139/v03-200.
Testo completoTomé, 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. 04n05 (aprile 2009): 408–14. http://dx.doi.org/10.1142/s1088424609000619.
Testo completoHou, 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. 6 (2020): 1135–39. http://dx.doi.org/10.1039/c9ob02490e.
Testo completoBednarek, Melania, e Przemysław Kubisa. "Reversible networks of degradable polyesters containing weak covalent bonds". Polymer Chemistry 10, n. 15 (2019): 1848–72. http://dx.doi.org/10.1039/c8py01731j.
Testo completoBauer, 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. 10 (20 maggio 2021): 3047. http://dx.doi.org/10.3390/molecules26103047.
Testo completoPetko, 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. 12 (dicembre 2018): 1115–21. http://dx.doi.org/10.1139/cjc-2018-0117.
Testo completoHamzehloueian, 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. 8 (2014): 911–24. http://dx.doi.org/10.2298/jsc140121012h.
Testo completoJursic, Branko S. "AM1 semiempirical study of benzopyrroles as dienes for Diels-Alder reaction". Canadian Journal of Chemistry 74, n. 1 (1 gennaio 1996): 114–20. http://dx.doi.org/10.1139/v96-015.
Testo completoBrossard, 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. 26 (2017): 5585–92. http://dx.doi.org/10.1039/c7ob01236e.
Testo completoKoçak, Ramazan, e Arif Daştan. "Synthesis of dibenzosuberenone-based novel polycyclic π-conjugated dihydropyridazines, pyridazines and pyrroles". Beilstein Journal of Organic Chemistry 17 (15 marzo 2021): 719–29. http://dx.doi.org/10.3762/bjoc.17.61.
Testo completoGribble, G. W. "Novel chemistry of indole in the synthesis of heterocycles". Pure and Applied Chemistry 75, n. 10 (1 gennaio 2003): 1417–32. http://dx.doi.org/10.1351/pac200375101417.
Testo completoÇapan, İrfan, e Süleyman Servi. "Synthesis of New C2-Symmetric Chiral Benzimidazole Derivatives Having Norbornene/Dibenzobarrelene Skeletons". Letters in Organic Chemistry 17, n. 10 (17 novembre 2020): 801–5. http://dx.doi.org/10.2174/1570178616666190731105327.
Testo completoMlostoń, Grzegorz, Yuriy Shermolovich e Heinz Heimgartner. "Synthesis of Fluorinated and Fluoroalkylated Heterocycles Containing at Least One Sulfur Atom via Cycloaddition Reactions". Materials 15, n. 20 (17 ottobre 2022): 7244. http://dx.doi.org/10.3390/ma15207244.
Testo completoKorol, 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. 4 (26 dicembre 2020): 146–54. http://dx.doi.org/10.25135/acg.oc.88.20.11.1870.
Testo completoBeck, Janina, Olaf Fuhr, Martin Nieger e Stefan Bräse. "A versatile Diels–Alder approach to functionalized hydroanthraquinones". Royal Society Open Science 7, n. 11 (novembre 2020): 200626. http://dx.doi.org/10.1098/rsos.200626.
Testo completoSpino, 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. 7 (1 luglio 1993): 1094–97. http://dx.doi.org/10.1139/v93-145.
Testo completoBates, 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. 5 (1998): 383. http://dx.doi.org/10.1071/c97128.
Testo completoMoore, 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. 83 (2014): 12523–25. http://dx.doi.org/10.1039/c4cc05906a.
Testo completode 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. 8 (agosto 2009): 1135–43. http://dx.doi.org/10.1139/v09-070.
Testo completoCharlton, 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. 6 (1 giugno 1993): 827–33. http://dx.doi.org/10.1139/v93-110.
Testo completoZeller, 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. 4 (15 marzo 2006): o1369—o1370. http://dx.doi.org/10.1107/s1600536806008014.
Testo completoGillard, 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. 9 (1 settembre 1991): 1337–43. http://dx.doi.org/10.1139/v91-199.
Testo completoJasiński, Radomir. "On the Question of Stepwise [4+2] Cycloaddition Reactions and Their Stereochemical Aspects". Symmetry 13, n. 10 (11 ottobre 2021): 1911. http://dx.doi.org/10.3390/sym13101911.
Testo completoWard, 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. 7 (1 luglio 1996): 1418–36. http://dx.doi.org/10.1139/v96-160.
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