Artigos de revistas sobre o tema "Cycloadditions aza-Diels–Alder"
Crie uma referência precisa em APA, MLA, Chicago, Harvard, e outros estilos
Veja os 50 melhores artigos de revistas para estudos sobre o assunto "Cycloadditions aza-Diels–Alder".
Ao lado de cada fonte na lista de referências, há um botão "Adicionar à bibliografia". Clique e geraremos automaticamente a citação bibliográfica do trabalho escolhido no estilo de citação de que você precisa: APA, MLA, Harvard, Chicago, Vancouver, etc.
Você também pode baixar o texto completo da publicação científica em formato .pdf e ler o resumo do trabalho online se estiver presente nos metadados.
Veja os artigos de revistas das mais diversas áreas científicas e compile uma bibliografia correta.
Heredia-Moya, Jorge, Daniel A. Zurita, José Eduardo Cadena-Cruz e Christian D. Alcívar-León. "Diaza-1,3-butadienes as Useful Intermediate in Heterocycles Synthesis". Molecules 27, n.º 19 (9 de outubro de 2022): 6708. http://dx.doi.org/10.3390/molecules27196708.
Texto completo da fontePresset, Marc, Michel Rajzmann, Guillaume Dauvergne, Jean Rodriguez e Yoann Coquerel. "Periselectivity in the Aza-Diels–Alder Reaction of 1-Azadienes with α-Oxoketenes: A Combined Experimental and Theoretical Study". Molecules 25, n.º 20 (20 de outubro de 2020): 4811. http://dx.doi.org/10.3390/molecules25204811.
Texto completo da fonteSkrzyńska, Anna, Sebastian Frankowski e Łukasz Albrecht. "Cyclic 1‐Azadienes in the Organocatalytic Inverse‐Electron‐Demand Aza‐Diels‐Alder Cycloadditions". Asian Journal of Organic Chemistry 9, n.º 11 (4 de setembro de 2020): 1688–700. http://dx.doi.org/10.1002/ajoc.202000332.
Texto completo da fonteCHEMOURI, HAFIDA, WAFAA BENCHOUK e SIDI MOHAMED MEKELLECHE. "REGIOSELECTIVITY OF HETERO DIELS–ALDER REACTIONS BETWEEN 1-AZA-1,3-BUTADIENE DERIVATIVES AND DIMETHYLVINYLAMINE: A THEORETICAL INVESTIGATION". Journal of Theoretical and Computational Chemistry 05, n.º 04 (dezembro de 2006): 707–18. http://dx.doi.org/10.1142/s0219633606002581.
Texto completo da fonteSousa, Carlos A. D., M. Luísa C. Vale, José E. Rodríguez-Borges, Xerardo Garcia-Mera e Jesús Rodríguez-Otero. "Acid-catalyzed aza-Diels–Alder versus 1,3-dipolar cycloadditions of methyl glyoxylate oxime with cyclopentadiene". Tetrahedron Letters 49, n.º 40 (setembro de 2008): 5777–81. http://dx.doi.org/10.1016/j.tetlet.2008.07.110.
Texto completo da fonteMayr, Herbert, Armin R. Ofial, Jürgen Sauer e Bernhard Schmied. "[2++4] Cycloadditions of Iminium Ions − Concerted or Stepwise Mechanism of Aza Diels−Alder Reactions?" European Journal of Organic Chemistry 2000, n.º 11 (junho de 2000): 2013–20. http://dx.doi.org/10.1002/1099-0690(200006)2000:11<2013::aid-ejoc2013>3.0.co;2-a.
Texto completo da fonteBlanco-Carapia, Roberto E., Enrique A. Aguilar-Rangel, Mónica A. Rincón-Guevara, Alejandro Islas-Jácome e Eduardo González-Zamora. "Synthesis of New Polyheterocyclic Pyrrolo[3,4-b]pyridin-5-ones via an Ugi-Zhu/Cascade/Click Strategy". Molecules 28, n.º 10 (14 de maio de 2023): 4087. http://dx.doi.org/10.3390/molecules28104087.
Texto completo da fonteFillion, Houda, Félix Pautet, Pascal Nebois e Zouhair Bouaziz. "Cycloadditions of α,β-Unsaturated N,N-Dimethylhydrazones. A Diels-Alder Strategy for the Building of Aza-Hetero Rings". HETEROCYCLES 54, n.º 2 (2001): 1095. http://dx.doi.org/10.3987/rev-00-sr(i)5.
Texto completo da fonteNtirampebura, Deogratias, e Léon Ghosez. "Cycloadditions of 2-aza-1,3-dienes to aldehydes: a Diels-Alder strategy for the diastereoselective hydroxyalkylation of carboxylic acid derivatives". Tetrahedron Letters 40, n.º 39 (setembro de 1999): 7079–82. http://dx.doi.org/10.1016/s0040-4039(99)01444-6.
Texto completo da fontePalacios, Francisco, Concepción Alonso, Patricia Amezua e Gloria Rubiales. "Synthesis of Aza Polycyclic Compounds Derived from Pyrrolidine, Indolizidine, and Indole via Intramolecular Diels−Alder Cycloadditions of Neutral 2-Azadienes". Journal of Organic Chemistry 67, n.º 6 (março de 2002): 1941–46. http://dx.doi.org/10.1021/jo016325v.
Texto completo da fonteSkrzyńska, Anna, Sebastian Frankowski e Łukasz Albrecht. "Front Cover: Cyclic 1‐Azadienes in the Organocatalytic Inverse‐Electron‐Demand Aza‐Diels‐Alder Cycloadditions (Asian J. Org. Chem. 11/2020)". Asian Journal of Organic Chemistry 9, n.º 11 (novembro de 2020): 1665. http://dx.doi.org/10.1002/ajoc.202000528.
Texto completo da fontePautet, Felix, Pascal Nebois, Zouhair Bouaziz e Houda Fillion. "ChemInform Abstract: Cycloadditions of α,β-Unsaturated N,N-Dimethylhydrazones. A Diels-Alder Strategy for the Building of Aza-hetero Rings". ChemInform 32, n.º 21 (26 de maio de 2010): no. http://dx.doi.org/10.1002/chin.200121258.
Texto completo da fontePalacios, Francisco, Concepcion Alonso, Patricia Amezua e Gloria Rubiales. "ChemInform Abstract: Synthesis of Aza Polycyclic Compounds Derived from Pyrrolidine, Indolizidine, and Indole via Intramolecular Diels-Alder Cycloadditions of Neutral 2-Azadienes." ChemInform 33, n.º 34 (20 de maio de 2010): no. http://dx.doi.org/10.1002/chin.200234164.
Texto completo da fonteNtirampebura, Deogratias, e Leon Ghosez. "ChemInform Abstract: Cycloadditions of 2-Aza-1,3-dienes to Aldehydes: A Diels-Alder Strategy for the Diastereoselective Hydroxyalkylation of Carboxylic Acid Derivatives." ChemInform 30, n.º 48 (12 de junho de 2010): no. http://dx.doi.org/10.1002/chin.199948163.
Texto completo da fonteHamzik, Philip J., Anne-Sophie Goutierre, Takeo Sakai e Rick L. Danheiser. "Aza Diels–Alder Reactions of Nitriles, N,N-Dimethylhydrazones, and Oximino Ethers. Application in Formal [2 + 2 + 2] Cycloadditions for the Synthesis of Pyridines". Journal of Organic Chemistry 82, n.º 24 (dezembro de 2017): 12975–91. http://dx.doi.org/10.1021/acs.joc.7b02503.
Texto completo da fonteABRAHAM, H., E. THEUS e L. STELLA. "ChemInform Abstract: Synthesis of Picolinic Acid Derivatives via Aza Diels-Alder Reaction: Zinc Iodide Activated Cycloadditions Between Methyl N-(1-Phenylethyl)-. alpha.-iminoacetate and Electron Rich Dienes." ChemInform 26, n.º 14 (18 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199514044.
Texto completo da fonteYe, Rong, Jing Sun, Ying Han e Chao-Guo Yan. "Molecular diversity of TEMPO-mediated cycloaddition of ketohydrazones and 3-phenacylideneoxindoles". New Journal of Chemistry 45, n.º 11 (2021): 5075–80. http://dx.doi.org/10.1039/d0nj06036d.
Texto completo da fonteBack, Thomas G. "Design and synthesis of some biologically interesting natural and unnatural products based on organosulfur and selenium chemistry". Canadian Journal of Chemistry 87, n.º 12 (dezembro de 2009): 1657–74. http://dx.doi.org/10.1139/v09-133.
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 fonteZhang, Xiaofeng, Gagan Dhawan, Alex Muthengi, Shuai Liu, Wei Wang, Marc Legris e Wei Zhang. "One-pot and catalyst-free synthesis of pyrroloquinolinediones and quinolinedicarboxylates". Green Chemistry 19, n.º 16 (2017): 3851–55. http://dx.doi.org/10.1039/c7gc01380a.
Texto completo da fonteVázquez-Vera, Óscar, Daniel Segura-Olvera, Mónica Rincón-Guevara, Atilano Gutiérrez-Carrillo, Miguel García-Sánchez, Ilich Ibarra, Leticia Lomas-Romero, Alejandro Islas-Jácome e Eduardo González-Zamora. "Synthesis of New 5-Aryl-benzo[f][1,7]naphthyridines via a Cascade Process (Ugi-3CR/Intramolecular Aza-Diels-Alder Cycloaddition)/Aromatization". Molecules 23, n.º 8 (14 de agosto de 2018): 2029. http://dx.doi.org/10.3390/molecules23082029.
Texto completo da fonteWu, Xiang, Shi-Bao Zhao, Lang-Lang Zheng e You-Gui Li. "Oxidative Asymmetric Formal Aza-Diels–Alder Reactions of Tetrahydro-β-carboline with Enones in the Synthesis of Indoloquinolizidine-2-ones". Molecules 23, n.º 9 (1 de setembro de 2018): 2228. http://dx.doi.org/10.3390/molecules23092228.
Texto completo da fonteKumar, Kamal, Mohammad Rehan, Jana Flegel, Franziska Heitkamp, Jorgelina L. Pergomet, Felix Otte e Carsten Strohmann. "Asymmetric Synthesis of 3,3′-Piperidinoyl Spirooxindoles and Discovery of Stereospecific Cycloadducts as Novel Hedgehog Pathway Modulators". Synthesis 52, n.º 21 (10 de agosto de 2020): 3140–52. http://dx.doi.org/10.1055/s-0040-1707222.
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 fonteFochi, Mariafrancesca, Luca Bernardi e Lorenzo Caruana. "Catalytic Asymmetric Aza-Diels–Alder Reactions: The Povarov Cycloaddition Reaction". Synthesis 46, n.º 02 (10 de dezembro de 2013): 135–57. http://dx.doi.org/10.1055/s-0033-1338581.
Texto completo da fonteIslas-Jácome, Perla, Cecilia García-Falcón, Sandra L. Castañón-Alonso, Ernesto Calderón-Jaimes, Daniel Canseco-González, Alejandro Islas-Jácome e Eduardo González-Zamora. "2-Benzyl-7-(4-chlorophenyl)-3-morpholino-6-((1-phenyl-1H-1,2,3-triazol-4-yl)methyl)-6,7-dihydro-5H-pyrrolo[3,4-b]pyridin-5-one". Molbank 2023, n.º 3 (10 de julho de 2023): M1693. http://dx.doi.org/10.3390/m1693.
Texto completo da fonteMorales-Salazar, Ivette, Mónica A. Rincón-Guevara, Eduardo González-Zamora e Alejandro Islas-Jácome. "2-Benzyl-3-morpholino-7-(thiophen-2-yl)-6-(thiophen-2-ylmethyl)-6,7-dihydro-5H-pyrrolo[3,4-b]pyridin-5-one". Molbank 2022, n.º 4 (23 de novembro de 2022): M1503. http://dx.doi.org/10.3390/m1503.
Texto completo da fonteFrankowski, Sebastian, Anna Skrzyńska, Lesław Sieroń e Łukasz Albrecht. "Deconjugated‐Ketone‐Derived Dienolates in Remote, Stereocontrolled, Aromative aza ‐Diels‐Alder Cycloaddition". Advanced Synthesis & Catalysis 362, n.º 13 (5 de maio de 2020): 2658–65. http://dx.doi.org/10.1002/adsc.202000197.
Texto completo da fonteFochi, Mariafrancesca, Lorenzo Caruana e Luca Bernardi. "ChemInform Abstract: Catalytic Asymmetric Aza-Diels-Alder Reactions: The Povarov Cycloaddition Reaction". ChemInform 45, n.º 15 (27 de março de 2014): no. http://dx.doi.org/10.1002/chin.201415264.
Texto completo da fonteBarešić, Luka, Davor Margetić e Zoran Glasovac. "Anion-Controlled Synthesis of Novel Guanidine-Substituted Oxanorbornanes". International Journal of Molecular Sciences 23, n.º 24 (16 de dezembro de 2022): 16036. http://dx.doi.org/10.3390/ijms232416036.
Texto completo da fonteRentería-Gómez, Manuel A., Shrikant G. Pharande, Alejandro Islas-Jácome, Eduardo González-Zamora e Rocío Gámez-Montaño. "MW-Assisted Synthesis of Eight New 6-Nitrilmethyl Pyrrolo[3,4-b]pyridin-5-Ones via a Domino Process: aza Diels–Alder/N-Acylation/Aromatization". Proceedings 9, n.º 1 (14 de novembro de 2018): 5. http://dx.doi.org/10.3390/ecsoc-22-05779.
Texto completo da fonteKhramtsova, Ekaterina E., Aleksandr D. Krainov, Maksim V. Dmitriev e Andrey N. Maslivets. "Cycloaddition of 4-Acyl-1H-pyrrole-2,3-diones Fused at [e]-Side and Cyanamides: Divergent Approach to 4H-1,3-Oxazines". Molecules 27, n.º 16 (17 de agosto de 2022): 5257. http://dx.doi.org/10.3390/molecules27165257.
Texto completo da fonteBarluenga, José, Francisco J. González, Santos Fustero e Vicente Gotor. "Diels–Alder cycloaddition reaction of unactivated 2-aza-1,3-dienes with dialkyl azodicarboxylates and heterocumulenes". J. Chem. Soc., Chem. Commun., n.º 15 (1986): 1179–80. http://dx.doi.org/10.1039/c39860001179.
Texto completo da fonteMorales-Salazar, Ivette, Carlos E. Garduño-Albino, Flora P. Montes-Enríquez, Dania A. Nava-Tapia, Napoleón Navarro-Tito, Leonardo David Herrera-Zúñiga, Eduardo González-Zamora e Alejandro Islas-Jácome. "Synthesis of Pyrrolo[3,4-b]pyridin-5-ones via Ugi–Zhu Reaction and In Vitro–In Silico Studies against Breast Carcinoma". Pharmaceuticals 16, n.º 11 (6 de novembro de 2023): 1562. http://dx.doi.org/10.3390/ph16111562.
Texto completo da fonteLepifre, Franck, Christophe Buon, Pierre-Yves Roger, Pascal Bouyssou e Gérard Coudert. "Easy access to N-aryl, N-heteroarylbenzoxazolinones and 4-aza analogues via Diels–Alder cycloaddition reactions". Tetrahedron Letters 45, n.º 44 (outubro de 2004): 8257–59. http://dx.doi.org/10.1016/j.tetlet.2004.08.162.
Texto completo da fonteMakino, Kazuishi, Yoshiaki Henmi, Makiko Terasawa, Osamu Hara e Yasumasa Hamada. "Remarkable effects of titanium tetrachloride in diastereoselective aza Diels–Alder cycloaddition: synthesis of (S)-piperazic acid". Tetrahedron Letters 46, n.º 4 (janeiro de 2005): 555–58. http://dx.doi.org/10.1016/j.tetlet.2004.12.003.
Texto completo da fonteGonzález-Zamora, Eduardo, Alejandro Islas-Jácome, Atilano Gutiérrez-Carrillo e Miguel García-Garibay. "One-Pot Synthesis of Nuevamine Aza-Analogues by Combined Use of an Oxidative Ugi Type Reaction and Aza-Diels–Alder Cycloaddition". Synlett 25, n.º 03 (2 de dezembro de 2013): 403–6. http://dx.doi.org/10.1055/s-0033-1340218.
Texto completo da fonteVil', Vera A., Sergei S. Grishin, Elena P. Baberkina, Anna L. Alekseenko, Alexey P. Glinushkin, Alexey E. Kovalenko e Alexander O. Terent'ev. "Electrochemical Synthesis of Tetrahydroquinolines from Imines and Cyclic Ethers via Oxidation/Aza‐Diels‐Alder Cycloaddition". Advanced Synthesis & Catalysis 364, n.º 6 (20 de janeiro de 2022): 1098–108. http://dx.doi.org/10.1002/adsc.202101355.
Texto completo da fonteKiran, I. N. Chaithanya, R. Santhosh Reddy, Chandraiah Lagishetti, Huacheng Xu, Zhen Wang e Yun He. "Selective Aza Diels–Alder and Domino [4+2]/[2+2] Cycloaddition Reactions of Arynes with N-Sulfonyl Ketimines". Journal of Organic Chemistry 82, n.º 3 (26 de janeiro de 2017): 1823–32. http://dx.doi.org/10.1021/acs.joc.6b02667.
Texto completo da fonteIslas-Jacome, Alejandro, Atilano Gutierrez-Carrillo, Miguel A. Garcia-Garibay e Eduardo Gonzalez-Zamora. "ChemInform Abstract: One-Pot Synthesis of Nuevamine Aza-Analogues by Combined Use of an Oxidative Ugi Type Reaction and Aza-Diels-Alder Cycloaddition." ChemInform 45, n.º 30 (10 de julho de 2014): no. http://dx.doi.org/10.1002/chin.201430162.
Texto completo da fonteCuerva, Juan M., Diego J. Cárdenas e Antonio M. Echavarren. "Intramolecular Michael-type addition of azadienes to 1,4-naphthoquinones instead of Aza-Diels–Alder cycloaddition: a synthesis of ascididemin". Journal of the Chemical Society, Perkin Transactions 1, n.º 11 (10 de maio de 2002): 1360–65. http://dx.doi.org/10.1039/b202555h.
Texto completo da fonteBoger, Dale L., Wendy L. Corbett e J. Mark Wiggins. "Room-temperature, endo-specific 1-aza-1,3-butadiene Diels-Alder reactions: acceleration of the LUMOdiene-controlled [4 + 2] cycloaddition reactions through noncomplementary aza diene substitution". Journal of Organic Chemistry 55, n.º 10 (maio de 1990): 2999–3000. http://dx.doi.org/10.1021/jo00297a006.
Texto completo da fonteSaito, Takao, Satoru Kobayashi, Takashi Otani, Hideoki Iwanami e Takayuki Soda. "Diene-Transmissive Hetero-Diels-Alder Cycloaddition Using Cross-Conjugated Dioxatrienes: A Novel Synthesis of Tetrahydropyran-Fused Aza- and Thia-heterocycles". HETEROCYCLES 76, n.º 1 (2008): 227. http://dx.doi.org/10.3987/com-08-s(n)55.
Texto completo da fonteMorales-Salazar, Ivette, Carlos E. Garduño-Albino, Flora P. Montes-Enríquez, Atilano Gutiérrez-Carrillo, Yareli Rojas-Aguirre, Nancy Viridiana Estrada-Toledo, Jorge Sandoval-Basilio et al. "In Vitro and In Silico Studies of Bis-furyl-pyrrolo[3,4-b]pyridin-5-ones on Dengue Virus". Journal of the Mexican Chemical Society 68, n.º 1 (1 de janeiro de 2024): 170–83. http://dx.doi.org/10.29356/jmcs.v68i1.2103.
Texto completo da fonteSasaki, Michiko, Philip J. Hamzik, Hidaka Ikemoto, Samuel G. Bartko e Rick L. Danheiser. "Formal Bimolecular [2 + 2 + 2] Cycloaddition Strategy for the Synthesis of Pyridines: Intramolecular Propargylic Ene Reaction/Aza Diels–Alder Reaction Cascades". Organic Letters 20, n.º 19 (24 de setembro de 2018): 6244–49. http://dx.doi.org/10.1021/acs.orglett.8b02728.
Texto completo da fonteCastillo, Juan-Carlos, Brian Castro Agudelo, Jaime Gálvez, Yannick Carissan, Jean Rodriguez e Yoann Coquerel. "Periselectivity in the aza-Diels–Alder Cycloaddition between α-Oxoketenes and N-(5-Pyrazolyl)imines: A Combined Experimental and Theoretical Study". Journal of Organic Chemistry 85, n.º 11 (12 de maio de 2020): 7368–77. http://dx.doi.org/10.1021/acs.joc.0c00767.
Texto completo da fonteCuerva, Juan M., Diego J. Cardenas e Antonio M. Echavarren. "ChemInform Abstract: Intramolecular Michael-Type Addition of Azadienes to 1,4-Naphthoquinones Instead of Aza-Diels-Alder Cycloaddition: A Synthesis of Ascididemin." ChemInform 33, n.º 40 (19 de maio de 2010): no. http://dx.doi.org/10.1002/chin.200240216.
Texto completo da fonteBoger, Dale L., e Timothy T. Curran. "Diels-Alder reactions of 1-aza-1,3-butadienes: room temperature, endo-selective LUMOdiene-controlled [4 + 2] cycloaddition reactions of N-sulfonyl-4-(ethoxycarbonyl)-1-aza-1,3-butadienes". Journal of Organic Chemistry 55, n.º 20 (setembro de 1990): 5439–42. http://dx.doi.org/10.1021/jo00307a009.
Texto completo da fonteSingal, Kewal Krishan, Baldev Singh e Baldev Raj. "Studies in 1-Aza-1,3-butadienes: Diels-Alder Cycloaddition Reactions of 1,4-Diaryl-1-aza-1,3-butadienes with Aryl Sulphonyl Nitrosites Leading to the Synthesis of New Oxadiazines". Synthetic Communications 23, n.º 1 (janeiro de 1993): 107–14. http://dx.doi.org/10.1080/00397919308020408.
Texto completo da fonteCheng, Yea Shun, Eugene Ho, Patrick S. Mariano e Herman L. Ammon. "Mechanistic aspects of the boron trifluoride catalyzed, intermolecular Diels-Alder cycloaddition of an unactivated 2-aza 1,3-diene with electron-donating-substituted dienophiles". Journal of Organic Chemistry 50, n.º 26 (dezembro de 1985): 5678–86. http://dx.doi.org/10.1021/jo00350a049.
Texto completo da fonte