Articoli di riviste sul tema "Cycloadditions aza-Diels–Alder"
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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. 19 (9 ottobre 2022): 6708. http://dx.doi.org/10.3390/molecules27196708.
Presset, 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. 20 (20 ottobre 2020): 4811. http://dx.doi.org/10.3390/molecules25204811.
Skrzyńska, 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. 11 (4 settembre 2020): 1688–700. http://dx.doi.org/10.1002/ajoc.202000332.
CHEMOURI, 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. 04 (dicembre 2006): 707–18. http://dx.doi.org/10.1142/s0219633606002581.
Sousa, 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. 40 (settembre 2008): 5777–81. http://dx.doi.org/10.1016/j.tetlet.2008.07.110.
Mayr, 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. 11 (giugno 2000): 2013–20. http://dx.doi.org/10.1002/1099-0690(200006)2000:11<2013::aid-ejoc2013>3.0.co;2-a.
Blanco-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. 10 (14 maggio 2023): 4087. http://dx.doi.org/10.3390/molecules28104087.
Fillion, 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. 2 (2001): 1095. http://dx.doi.org/10.3987/rev-00-sr(i)5.
Ntirampebura, 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. 39 (settembre 1999): 7079–82. http://dx.doi.org/10.1016/s0040-4039(99)01444-6.
Palacios, 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. 6 (marzo 2002): 1941–46. http://dx.doi.org/10.1021/jo016325v.
Skrzyńska, 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. 11 (novembre 2020): 1665. http://dx.doi.org/10.1002/ajoc.202000528.
Pautet, 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. 21 (26 maggio 2010): no. http://dx.doi.org/10.1002/chin.200121258.
Palacios, 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. 34 (20 maggio 2010): no. http://dx.doi.org/10.1002/chin.200234164.
Ntirampebura, 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. 48 (12 giugno 2010): no. http://dx.doi.org/10.1002/chin.199948163.
Hamzik, 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. 24 (dicembre 2017): 12975–91. http://dx.doi.org/10.1021/acs.joc.7b02503.
ABRAHAM, 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. 14 (18 agosto 2010): no. http://dx.doi.org/10.1002/chin.199514044.
Ye, 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. 11 (2021): 5075–80. http://dx.doi.org/10.1039/d0nj06036d.
Back, 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. 12 (dicembre 2009): 1657–74. http://dx.doi.org/10.1139/v09-133.
Ayadi, 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.
Zhang, 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. 16 (2017): 3851–55. http://dx.doi.org/10.1039/c7gc01380a.
Vázquez-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. 8 (14 agosto 2018): 2029. http://dx.doi.org/10.3390/molecules23082029.
Wu, 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. 9 (1 settembre 2018): 2228. http://dx.doi.org/10.3390/molecules23092228.
Kumar, 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. 21 (10 agosto 2020): 3140–52. http://dx.doi.org/10.1055/s-0040-1707222.
Escalante, 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.
Fochi, Mariafrancesca, Luca Bernardi e Lorenzo Caruana. "Catalytic Asymmetric Aza-Diels–Alder Reactions: The Povarov Cycloaddition Reaction". Synthesis 46, n. 02 (10 dicembre 2013): 135–57. http://dx.doi.org/10.1055/s-0033-1338581.
Islas-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. 3 (10 luglio 2023): M1693. http://dx.doi.org/10.3390/m1693.
Morales-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. 4 (23 novembre 2022): M1503. http://dx.doi.org/10.3390/m1503.
Frankowski, 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. 13 (5 maggio 2020): 2658–65. http://dx.doi.org/10.1002/adsc.202000197.
Fochi, Mariafrancesca, Lorenzo Caruana e Luca Bernardi. "ChemInform Abstract: Catalytic Asymmetric Aza-Diels-Alder Reactions: The Povarov Cycloaddition Reaction". ChemInform 45, n. 15 (27 marzo 2014): no. http://dx.doi.org/10.1002/chin.201415264.
Barešić, Luka, Davor Margetić e Zoran Glasovac. "Anion-Controlled Synthesis of Novel Guanidine-Substituted Oxanorbornanes". International Journal of Molecular Sciences 23, n. 24 (16 dicembre 2022): 16036. http://dx.doi.org/10.3390/ijms232416036.
Rentería-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. 1 (14 novembre 2018): 5. http://dx.doi.org/10.3390/ecsoc-22-05779.
Khramtsova, 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. 16 (17 agosto 2022): 5257. http://dx.doi.org/10.3390/molecules27165257.
Barluenga, 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. 15 (1986): 1179–80. http://dx.doi.org/10.1039/c39860001179.
Morales-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. 11 (6 novembre 2023): 1562. http://dx.doi.org/10.3390/ph16111562.
Lepifre, 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. 44 (ottobre 2004): 8257–59. http://dx.doi.org/10.1016/j.tetlet.2004.08.162.
Makino, 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. 4 (gennaio 2005): 555–58. http://dx.doi.org/10.1016/j.tetlet.2004.12.003.
González-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. 03 (2 dicembre 2013): 403–6. http://dx.doi.org/10.1055/s-0033-1340218.
Vil', 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. 6 (20 gennaio 2022): 1098–108. http://dx.doi.org/10.1002/adsc.202101355.
Kiran, 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. 3 (26 gennaio 2017): 1823–32. http://dx.doi.org/10.1021/acs.joc.6b02667.
Islas-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. 30 (10 luglio 2014): no. http://dx.doi.org/10.1002/chin.201430162.
Cuerva, 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. 11 (10 maggio 2002): 1360–65. http://dx.doi.org/10.1039/b202555h.
Boger, 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. 10 (maggio 1990): 2999–3000. http://dx.doi.org/10.1021/jo00297a006.
Saito, 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. 1 (2008): 227. http://dx.doi.org/10.3987/com-08-s(n)55.
Morales-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. 1 (1 gennaio 2024): 170–83. http://dx.doi.org/10.29356/jmcs.v68i1.2103.
Sasaki, 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. 19 (24 settembre 2018): 6244–49. http://dx.doi.org/10.1021/acs.orglett.8b02728.
Castillo, 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. 11 (12 maggio 2020): 7368–77. http://dx.doi.org/10.1021/acs.joc.0c00767.
Cuerva, 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. 40 (19 maggio 2010): no. http://dx.doi.org/10.1002/chin.200240216.
Boger, 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. 20 (settembre 1990): 5439–42. http://dx.doi.org/10.1021/jo00307a009.
Singal, 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. 1 (gennaio 1993): 107–14. http://dx.doi.org/10.1080/00397919308020408.
Cheng, 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. 26 (dicembre 1985): 5678–86. http://dx.doi.org/10.1021/jo00350a049.