Relevant bibliographies by topics / Povarov-type

Academic literature on the topic 'Povarov-type'

Author: Grafiati
Published: 10 December 2022
Last updated: 29 January 2023

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Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Povarov-type.'

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Journal articles on the topic "Povarov-type"

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Clerigué, José, M. Teresa Ramos, and J. Carlos Menéndez. "(2S*,4S*)-4-[(E)-(2,2-Dimethylhydrazono)methyl]-6-methoxy-4-methyl-2-[(E)-styryl]-1,2,3,4-tetrahydroquinoline." Molbank 2021, no. 2 (June 1, 2021): M1220. http://dx.doi.org/10.3390/m1220.

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The Povarov reaction of p-anisidine, cinnamaldehyde and methacrolein dimethylhydrazone afforded a 1,2,3,4-tetrahydroquinoline derivative bearing 2-styryl, 4-methyl and 4-dimethylhydrazono substituents in a fully diastereoselective fashion. This is the first example of the combination of a type I aza-vinylogous Povarov reaction and a type II vinylogous Povarov reaction in the same process.
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Vicente-García, Esther, Federica Catti, Rosario Ramón, and Rodolfo Lavilla. "Unsaturated Lactams: New Inputs for Povarov-Type Multicomponent Reactions." Organic Letters 12, no. 4 (February 19, 2010): 860–63. http://dx.doi.org/10.1021/ol902913j.

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Sanz-Vidal, Álvaro, Javier Miró, María Sánchez-Roselló, Carlos del Pozo, and Santos Fustero. "Gold-Catalyzed Povarov-Type Reaction of Fluorinated Imino Esters and Furans." Journal of Organic Chemistry 81, no. 15 (July 22, 2016): 6515–24. http://dx.doi.org/10.1021/acs.joc.6b01139.

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Chandra, Devesh, Ankit Kumar Dhiman, Rakesh Kumar, and Upendra Sharma. "Microwave-Assisted Metal-Free Rapid Synthesis of C4-Arylated Quinolines via Povarov Type Multicomponent Reaction." European Journal of Organic Chemistry 2019, no. 16 (April 1, 2019): 2753–58. http://dx.doi.org/10.1002/ejoc.201900325.

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Galvez, Jaime, Juan-Carlos Castillo, Jairo Quiroga, Michel Rajzmann, Jean Rodriguez, and Yoann Coquerel. "Divergent Chemo-, Regio-, and Diastereoselective Normal Electron-Demand Povarov-Type Reactions with α-Oxo-ketene Dienophiles." Organic Letters 16, no. 16 (July 30, 2014): 4126–29. http://dx.doi.org/10.1021/ol5018245.

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Sridharan, Vellaisamy, Carmen Avendaño, and J. Carlos Menéndez. "Convenient, two-step synthesis of 2-styrylquinolines: an application of the CAN-catalyzed vinylogous type-II Povarov reaction." Tetrahedron 65, no. 10 (March 2009): 2087–96. http://dx.doi.org/10.1016/j.tet.2008.12.077.

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Galvez, Jaime, Juan-Carlos Castillo, Jairo Quiroga, Michel Rajzmann, Jean Rodriguez, and Yoann Coquerel. "ChemInform Abstract: Divergent Chemo-, Regio-, and Diastereoselective Normal Electron-Demand Povarov-Type Reactions with α-Oxo-ketene Dienophiles." ChemInform 46, no. 7 (January 29, 2015): no. http://dx.doi.org/10.1002/chin.201507231.

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Ghoshal, Anirban, Doddapaneni Yugandhar, Jagadeesh Babu Nanubolu, and Ajay Kumar Srivastava. "An Efficient One-Pot Synthesis of Densely Functionalized Fused-Quinolines via Sequential Ugi4CC and Acid-Mediated Povarov-Type Reaction." ACS Combinatorial Science 19, no. 9 (August 8, 2017): 600–608. http://dx.doi.org/10.1021/acscombsci.7b00095.

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Wu, Xia, Xiao Geng, Peng Zhao, Jingjing Zhang, Xingxing Gong, Yan-dong Wu, and An-xin Wu. "I2-Promoted Povarov-Type Reaction Using 1,4-Dithane-2,5-diol as an Ethylene Surrogate: Formal [4 + 2] Synthesis of Quinolines." Organic Letters 19, no. 7 (March 16, 2017): 1550–53. http://dx.doi.org/10.1021/acs.orglett.7b00361.

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Gao, Qinghe, Shan Liu, Xia Wu, and Anxin Wu. "Povarov-Type Reaction Using Methyl as New Input: Direct Synthesis of Substituted Quinolines by I2-Mediated Formal [3 + 2 + 1] Cycloaddition." Organic Letters 16, no. 17 (August 13, 2014): 4582–85. http://dx.doi.org/10.1021/ol502134u.

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Dissertations / Theses on the topic "Povarov-type"

1

Osborne, D. "Synthesis of novel heterocycles using Povarov type reactions." Thesis, Queen's University Belfast, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.403344.

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Journal articles
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