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Journal articles on the topic 'Pentannulation'

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Author: Grafiati
Published: 10 March 2023

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1

Lütke Eversloh, Christian, Yuri Avlasevich, Chen Li, and Klaus Müllen. "Palladium-Catalyzed Pentannulation of Polycyclic Aromatic Hydrocarbons." Chemistry - A European Journal 17, no. 45 (September 28, 2011): 12756–62. http://dx.doi.org/10.1002/chem.201101126.

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2

Pujanauski, Brian G., B. A. Bhanu Prasad, and Richmond Sarpong. "Pt-Catalyzed Tandem Epoxide Fragmentation/Pentannulation of Propargylic Esters." Journal of the American Chemical Society 128, no. 21 (May 2006): 6786–87. http://dx.doi.org/10.1021/ja061549m.

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3

Petrović, Martina, and Ernesto G. Occhiato. "Pentannulation of Heterocycles by Virtue of Precious Metal Catalysis." Chemistry - An Asian Journal 11, no. 5 (November 30, 2015): 642–59. http://dx.doi.org/10.1002/asia.201501127.

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4

Eversloh, Christian Luetke, Yuri Avlasevich, Chen Li, and Klaus Muellen. "ChemInform Abstract: Palladium-Catalyzed Pentannulation of Polycyclic Aromatic Hydrocarbons." ChemInform 43, no. 13 (March 1, 2012): no. http://dx.doi.org/10.1002/chin.201213115.

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5

Nakanishi, Yusuke, Koji Miki, and Kouichi Ohe. "Transition metal-catalyzed pentannulation of propargyl acetates via styrylcarbene intermediates." Tetrahedron 63, no. 49 (December 2007): 12138–48. http://dx.doi.org/10.1016/j.tet.2007.09.064.

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6

Angel, Mirana C., and Victor L. Prutyanov. "The DFT study on pentannulation reaction of tungsten Fischer carbene complexes." Computational and Theoretical Chemistry 1196 (February 2021): 113121. http://dx.doi.org/10.1016/j.comptc.2020.113121.

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7

Kazem Shiroodi, Roohollah, Masumi Sugawara, Maxim Ratushnyy, Douglas C. Yarbrough, Donald J. Wink, and Vladimir Gevorgyan. "Au-Catalyzed Pentannulation Reaction of Propargylic Esters Occurring at C(sp3)–H Site." Organic Letters 17, no. 16 (August 6, 2015): 4062–65. http://dx.doi.org/10.1021/acs.orglett.5b01983.

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8

Rinaldi, Antonia, Martina Petrović, Stefano Magnolfi, Dina Scarpi, and Ernesto G. Occhiato. "Pentannulation Reaction by Tandem Gold(I)-Catalyzed Propargyl Claisen Rearrangement/Nazarov Cyclization of Enynyl Vinyl Ethers." Organic Letters 20, no. 15 (July 23, 2018): 4713–17. http://dx.doi.org/10.1021/acs.orglett.8b02141.

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9

Fernandes, Rodney A., Sachin P. Gholap, Vijay P. Chavan, Akeel S. Saiyed, and Shubhankar Bhattacharyya. "Fischer Carbene Pentannulation with Alkynes Having Adjacent Carbonate or Acyloxy Groups: Synthesis of 3-Substituted 1-Indanones." Organic Letters 22, no. 9 (April 10, 2020): 3438–43. http://dx.doi.org/10.1021/acs.orglett.0c00901.

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10

Ghosh, Animesh, Atanu Basak, Kuheli Chakrabarty, Sonjoy Mondal, Arpita Chatterjee, and Gourab Kanti Das. "Au-Catalyzed Hexannulation and Pt-Catalyzed Pentannulation of Propargylic Ester Bearing a 2-Alkynyl-phenyl Substituent: A Comparative DFT Study." ACS Omega 3, no. 1 (January 29, 2018): 1159–69. http://dx.doi.org/10.1021/acsomega.7b01889.

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11

Zanella, Giovanna, Martina Petrović, Dina Scarpi, Ernesto G. Occhiato, and Enrique Gómez-Bengoa. "Pentannulation of N-heterocycles by a tandem gold-catalyzed [3,3]-rearrangement/Nazarov reaction of propargyl ester derivatives: a computational study on the crucial role of the nitrogen atom." Beilstein Journal of Organic Chemistry 16 (December 15, 2020): 3059–68. http://dx.doi.org/10.3762/bjoc.16.255.

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Abstract:
The tandem gold(I)-catalyzed rearrangement/Nazarov reaction of enynyl acetates in which the double bond is embedded in a piperidine ring was computationally and experimentally studied. The theoretical calculations predict that the position of the propargylic acetate substituent has a great impact on the reactivity. In contrast to our previous successful cyclization of the 2-substituted substrates, where the nitrogen favors the formation of the cyclized final product, the substitution at position 3 was computed to have a deleterious effect on the electronic properties of the molecules, increasing the activation barriers of the Nazarov reaction. The sluggish reactivity of 3-substituted piperidines predicted by the calculations was further confirmed by the results obtained with some designed substrates.
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12

Satpathi, Bishnupada, Lona Dutta, and S. S. V. Ramasastry. "Phosphine- and water-promoted pentannulative aldol reaction." Organic & Biomolecular Chemistry 17, no. 6 (2019): 1547–51. http://dx.doi.org/10.1039/c8ob03106a.

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13

Satpathi, Bishnupada, Lona Dutta, and S. S. V. Ramasastry. "Metal- and Hydride-Free Pentannulative Reductive Aldol Reaction." Organic Letters 21, no. 1 (December 13, 2018): 170–74. http://dx.doi.org/10.1021/acs.orglett.8b03658.

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14

Bhanu Prasad, B. A., Francis K. Yoshimoto, and Richmond Sarpong. "Pt-Catalyzed Pentannulations from In Situ Generated Metallo−Carbenoids Utilizing Propargylic Esters." Journal of the American Chemical Society 127, no. 36 (September 2005): 12468–69. http://dx.doi.org/10.1021/ja053192c.

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15

Pujanauski, Brian G., B. A. Bhanu Prasad, and Richmond Sarpong. "Pt-Catalyzed Tandem Epoxide Fragmentation/Pentannulation of Propargylic Esters." ChemInform 37, no. 39 (September 26, 2006). http://dx.doi.org/10.1002/chin.200639114.

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16

Petrovic, Martina, and Ernesto G. Occhiato. "ChemInform Abstract: Pentannulation of Heterocycles by Virtue of Precious Metal Catalysis." ChemInform 47, no. 19 (April 2016). http://dx.doi.org/10.1002/chin.201619202.

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17

Nakanishi, Yusuke, Koji Miki, and Kouichi Ohe. "ChemInform Abstract: Transition Metal Catalyzed Pentannulation of Propargyl Acetates via Styrylcarbene Intermediates." ChemInform 39, no. 10 (March 4, 2008). http://dx.doi.org/10.1002/chin.200810096.

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18

Kazem Shiroodi, Roohollah, Masumi Sugawara, Maxim Ratushnyy, Douglas C. Yarbrough, Donald J. Wink, and Vladimir Gevorgyan. "ChemInform Abstract: Au-Catalyzed Pentannulation Reaction of Propargylic Esters Occurring at C(sp3)-H Site." ChemInform 47, no. 2 (January 2, 2016). http://dx.doi.org/10.1002/chin.201602035.

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19

Prasad, B. A. Bhanu, Francis K. Yoshimoto, and Richmond Sarpong. "Pt-Catalyzed Pentannulations from in situ Generated Metallo—Carbenoids Utilizing Propargylic Esters." ChemInform 37, no. 3 (January 17, 2006). http://dx.doi.org/10.1002/chin.200603077.

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