Статті в журналах з теми "Aza-Diels–Alder cycloadditions"
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Heredia-Moya, Jorge, Daniel A. Zurita, José Eduardo Cadena-Cruz, and Christian D. Alcívar-León. "Diaza-1,3-butadienes as Useful Intermediate in Heterocycles Synthesis." Molecules 27, no. 19 (October 9, 2022): 6708. http://dx.doi.org/10.3390/molecules27196708.
Повний текст джерелаPresset, Marc, Michel Rajzmann, Guillaume Dauvergne, Jean Rodriguez та Yoann Coquerel. "Periselectivity in the Aza-Diels–Alder Reaction of 1-Azadienes with α-Oxoketenes: A Combined Experimental and Theoretical Study". Molecules 25, № 20 (20 жовтня 2020): 4811. http://dx.doi.org/10.3390/molecules25204811.
Повний текст джерелаSkrzyńska, Anna, Sebastian Frankowski, and Łukasz Albrecht. "Cyclic 1‐Azadienes in the Organocatalytic Inverse‐Electron‐Demand Aza‐Diels‐Alder Cycloadditions." Asian Journal of Organic Chemistry 9, no. 11 (September 4, 2020): 1688–700. http://dx.doi.org/10.1002/ajoc.202000332.
Повний текст джерелаCHEMOURI, HAFIDA, WAFAA BENCHOUK, and 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, no. 04 (December 2006): 707–18. http://dx.doi.org/10.1142/s0219633606002581.
Повний текст джерелаSousa, Carlos A. D., M. Luísa C. Vale, José E. Rodríguez-Borges, Xerardo Garcia-Mera, and Jesús Rodríguez-Otero. "Acid-catalyzed aza-Diels–Alder versus 1,3-dipolar cycloadditions of methyl glyoxylate oxime with cyclopentadiene." Tetrahedron Letters 49, no. 40 (September 2008): 5777–81. http://dx.doi.org/10.1016/j.tetlet.2008.07.110.
Повний текст джерелаMayr, Herbert, Armin R. Ofial, Jürgen Sauer, and Bernhard Schmied. "[2++4] Cycloadditions of Iminium Ions − Concerted or Stepwise Mechanism of Aza Diels−Alder Reactions?" European Journal of Organic Chemistry 2000, no. 11 (June 2000): 2013–20. http://dx.doi.org/10.1002/1099-0690(200006)2000:11<2013::aid-ejoc2013>3.0.co;2-a.
Повний текст джерелаBlanco-Carapia, Roberto E., Enrique A. Aguilar-Rangel, Mónica A. Rincón-Guevara, Alejandro Islas-Jácome, and Eduardo González-Zamora. "Synthesis of New Polyheterocyclic Pyrrolo[3,4-b]pyridin-5-ones via an Ugi-Zhu/Cascade/Click Strategy." Molecules 28, no. 10 (May 14, 2023): 4087. http://dx.doi.org/10.3390/molecules28104087.
Повний текст джерелаFillion, Houda, Félix Pautet, Pascal Nebois та Zouhair Bouaziz. "Cycloadditions of α,β-Unsaturated N,N-Dimethylhydrazones. A Diels-Alder Strategy for the Building of Aza-Hetero Rings". HETEROCYCLES 54, № 2 (2001): 1095. http://dx.doi.org/10.3987/rev-00-sr(i)5.
Повний текст джерелаNtirampebura, Deogratias, and 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, no. 39 (September 1999): 7079–82. http://dx.doi.org/10.1016/s0040-4039(99)01444-6.
Повний текст джерелаPalacios, Francisco, Concepción Alonso, Patricia Amezua, and 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, no. 6 (March 2002): 1941–46. http://dx.doi.org/10.1021/jo016325v.
Повний текст джерелаSkrzyńska, Anna, Sebastian Frankowski, and 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, no. 11 (November 2020): 1665. http://dx.doi.org/10.1002/ajoc.202000528.
Повний текст джерелаPautet, Felix, Pascal Nebois, Zouhair Bouaziz та 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, № 21 (26 травня 2010): no. http://dx.doi.org/10.1002/chin.200121258.
Повний текст джерелаPalacios, Francisco, Concepcion Alonso, Patricia Amezua, and 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, no. 34 (May 20, 2010): no. http://dx.doi.org/10.1002/chin.200234164.
Повний текст джерелаNtirampebura, Deogratias, and 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, no. 48 (June 12, 2010): no. http://dx.doi.org/10.1002/chin.199948163.
Повний текст джерелаHamzik, Philip J., Anne-Sophie Goutierre, Takeo Sakai, and 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, no. 24 (December 2017): 12975–91. http://dx.doi.org/10.1021/acs.joc.7b02503.
Повний текст джерелаABRAHAM, H., E. THEUS, and 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, no. 14 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199514044.
Повний текст джерелаYe, Rong, Jing Sun, Ying Han, and Chao-Guo Yan. "Molecular diversity of TEMPO-mediated cycloaddition of ketohydrazones and 3-phenacylideneoxindoles." New Journal of Chemistry 45, no. 11 (2021): 5075–80. http://dx.doi.org/10.1039/d0nj06036d.
Повний текст джерелаBack, Thomas G. "Design and synthesis of some biologically interesting natural and unnatural products based on organosulfur and selenium chemistry." Canadian Journal of Chemistry 87, no. 12 (December 2009): 1657–74. http://dx.doi.org/10.1139/v09-133.
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 джерелаZhang, Xiaofeng, Gagan Dhawan, Alex Muthengi, Shuai Liu, Wei Wang, Marc Legris, and Wei Zhang. "One-pot and catalyst-free synthesis of pyrroloquinolinediones and quinolinedicarboxylates." Green Chemistry 19, no. 16 (2017): 3851–55. http://dx.doi.org/10.1039/c7gc01380a.
Повний текст джерелаVázquez-Vera, Óscar, Daniel Segura-Olvera, Mónica Rincón-Guevara, Atilano Gutiérrez-Carrillo, Miguel García-Sánchez, Ilich Ibarra, Leticia Lomas-Romero, Alejandro Islas-Jácome, and 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, no. 8 (August 14, 2018): 2029. http://dx.doi.org/10.3390/molecules23082029.
Повний текст джерелаWu, Xiang, Shi-Bao Zhao, Lang-Lang Zheng та 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, № 9 (1 вересня 2018): 2228. http://dx.doi.org/10.3390/molecules23092228.
Повний текст джерелаKumar, Kamal, Mohammad Rehan, Jana Flegel, Franziska Heitkamp, Jorgelina L. Pergomet, Felix Otte, and Carsten Strohmann. "Asymmetric Synthesis of 3,3′-Piperidinoyl Spirooxindoles and Discovery of Stereospecific Cycloadducts as Novel Hedgehog Pathway Modulators." Synthesis 52, no. 21 (August 10, 2020): 3140–52. http://dx.doi.org/10.1055/s-0040-1707222.
Повний текст джерелаEscalante, Carlos H., Eder I. Martínez-Mora, Carlos Espinoza-Hicks, Alejandro A. Camacho-Dávila, Fernando R. Ramos-Morales, Francisco Delgado, and 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 (June 17, 2020): 1320–34. http://dx.doi.org/10.3762/bjoc.16.113.
Повний текст джерелаFochi, Mariafrancesca, Luca Bernardi, and Lorenzo Caruana. "Catalytic Asymmetric Aza-Diels–Alder Reactions: The Povarov Cycloaddition Reaction." Synthesis 46, no. 02 (December 10, 2013): 135–57. http://dx.doi.org/10.1055/s-0033-1338581.
Повний текст джерелаIslas-Jácome, Perla, Cecilia García-Falcón, Sandra L. Castañón-Alonso, Ernesto Calderón-Jaimes, Daniel Canseco-González, Alejandro Islas-Jácome, and 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, no. 3 (July 10, 2023): M1693. http://dx.doi.org/10.3390/m1693.
Повний текст джерелаMorales-Salazar, Ivette, Mónica A. Rincón-Guevara, Eduardo González-Zamora, and 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, no. 4 (November 23, 2022): M1503. http://dx.doi.org/10.3390/m1503.
Повний текст джерелаFrankowski, Sebastian, Anna Skrzyńska, Lesław Sieroń, and Łukasz Albrecht. "Deconjugated‐Ketone‐Derived Dienolates in Remote, Stereocontrolled, Aromative aza ‐Diels‐Alder Cycloaddition." Advanced Synthesis & Catalysis 362, no. 13 (May 5, 2020): 2658–65. http://dx.doi.org/10.1002/adsc.202000197.
Повний текст джерелаFochi, Mariafrancesca, Lorenzo Caruana, and Luca Bernardi. "ChemInform Abstract: Catalytic Asymmetric Aza-Diels-Alder Reactions: The Povarov Cycloaddition Reaction." ChemInform 45, no. 15 (March 27, 2014): no. http://dx.doi.org/10.1002/chin.201415264.
Повний текст джерелаBarešić, Luka, Davor Margetić, and Zoran Glasovac. "Anion-Controlled Synthesis of Novel Guanidine-Substituted Oxanorbornanes." International Journal of Molecular Sciences 23, no. 24 (December 16, 2022): 16036. http://dx.doi.org/10.3390/ijms232416036.
Повний текст джерелаRentería-Gómez, Manuel A., Shrikant G. Pharande, Alejandro Islas-Jácome, Eduardo González-Zamora, and 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, no. 1 (November 14, 2018): 5. http://dx.doi.org/10.3390/ecsoc-22-05779.
Повний текст джерелаKhramtsova, Ekaterina E., Aleksandr D. Krainov, Maksim V. Dmitriev, and 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, no. 16 (August 17, 2022): 5257. http://dx.doi.org/10.3390/molecules27165257.
Повний текст джерелаBarluenga, José, Francisco J. González, Santos Fustero, and Vicente Gotor. "Diels–Alder cycloaddition reaction of unactivated 2-aza-1,3-dienes with dialkyl azodicarboxylates and heterocumulenes." J. Chem. Soc., Chem. Commun., no. 15 (1986): 1179–80. http://dx.doi.org/10.1039/c39860001179.
Повний текст джерелаMorales-Salazar, Ivette, Carlos E. Garduño-Albino, Flora P. Montes-Enríquez, Dania A. Nava-Tapia, Napoleón Navarro-Tito, Leonardo David Herrera-Zúñiga, Eduardo González-Zamora, and 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, no. 11 (November 6, 2023): 1562. http://dx.doi.org/10.3390/ph16111562.
Повний текст джерелаLepifre, Franck, Christophe Buon, Pierre-Yves Roger, Pascal Bouyssou, and Gérard Coudert. "Easy access to N-aryl, N-heteroarylbenzoxazolinones and 4-aza analogues via Diels–Alder cycloaddition reactions." Tetrahedron Letters 45, no. 44 (October 2004): 8257–59. http://dx.doi.org/10.1016/j.tetlet.2004.08.162.
Повний текст джерелаMakino, Kazuishi, Yoshiaki Henmi, Makiko Terasawa, Osamu Hara, and Yasumasa Hamada. "Remarkable effects of titanium tetrachloride in diastereoselective aza Diels–Alder cycloaddition: synthesis of (S)-piperazic acid." Tetrahedron Letters 46, no. 4 (January 2005): 555–58. http://dx.doi.org/10.1016/j.tetlet.2004.12.003.
Повний текст джерелаGonzález-Zamora, Eduardo, Alejandro Islas-Jácome, Atilano Gutiérrez-Carrillo, and 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, no. 03 (December 2, 2013): 403–6. http://dx.doi.org/10.1055/s-0033-1340218.
Повний текст джерелаVil', Vera A., Sergei S. Grishin, Elena P. Baberkina, Anna L. Alekseenko, Alexey P. Glinushkin, Alexey E. Kovalenko, and Alexander O. Terent'ev. "Electrochemical Synthesis of Tetrahydroquinolines from Imines and Cyclic Ethers via Oxidation/Aza‐Diels‐Alder Cycloaddition." Advanced Synthesis & Catalysis 364, no. 6 (January 20, 2022): 1098–108. http://dx.doi.org/10.1002/adsc.202101355.
Повний текст джерелаKiran, I. N. Chaithanya, R. Santhosh Reddy, Chandraiah Lagishetti, Huacheng Xu, Zhen Wang, and 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, no. 3 (January 26, 2017): 1823–32. http://dx.doi.org/10.1021/acs.joc.6b02667.
Повний текст джерелаIslas-Jacome, Alejandro, Atilano Gutierrez-Carrillo, Miguel A. Garcia-Garibay, and 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, no. 30 (July 10, 2014): no. http://dx.doi.org/10.1002/chin.201430162.
Повний текст джерелаCuerva, Juan M., Diego J. Cárdenas, and 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, no. 11 (May 10, 2002): 1360–65. http://dx.doi.org/10.1039/b202555h.
Повний текст джерелаBoger, Dale L., Wendy L. Corbett, and 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, no. 10 (May 1990): 2999–3000. http://dx.doi.org/10.1021/jo00297a006.
Повний текст джерелаSaito, Takao, Satoru Kobayashi, Takashi Otani, Hideoki Iwanami, and Takayuki Soda. "Diene-Transmissive Hetero-Diels-Alder Cycloaddition Using Cross-Conjugated Dioxatrienes: A Novel Synthesis of Tetrahydropyran-Fused Aza- and Thia-heterocycles." HETEROCYCLES 76, no. 1 (2008): 227. http://dx.doi.org/10.3987/com-08-s(n)55.
Повний текст джерелаMorales-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, no. 1 (January 1, 2024): 170–83. http://dx.doi.org/10.29356/jmcs.v68i1.2103.
Повний текст джерелаSasaki, Michiko, Philip J. Hamzik, Hidaka Ikemoto, Samuel G. Bartko, and 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, no. 19 (September 24, 2018): 6244–49. http://dx.doi.org/10.1021/acs.orglett.8b02728.
Повний текст джерелаCastillo, Juan-Carlos, Brian Castro Agudelo, Jaime Gálvez, Yannick Carissan, Jean Rodriguez та 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, № 11 (12 травня 2020): 7368–77. http://dx.doi.org/10.1021/acs.joc.0c00767.
Повний текст джерелаCuerva, Juan M., Diego J. Cardenas, and 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, no. 40 (May 19, 2010): no. http://dx.doi.org/10.1002/chin.200240216.
Повний текст джерелаBoger, Dale L., and 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, no. 20 (September 1990): 5439–42. http://dx.doi.org/10.1021/jo00307a009.
Повний текст джерелаSingal, Kewal Krishan, Baldev Singh, and 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, no. 1 (January 1993): 107–14. http://dx.doi.org/10.1080/00397919308020408.
Повний текст джерелаCheng, Yea Shun, Eugene Ho, Patrick S. Mariano, and 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, no. 26 (December 1985): 5678–86. http://dx.doi.org/10.1021/jo00350a049.
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