Relevant bibliographies by topics / Vinylcyclopropane Reactivity

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'Vinylcyclopropane Reactivity'

Author: Grafiati
Published: 4 June 2021
Last updated: 6 September 2023

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Journal articles on the topic "Vinylcyclopropane Reactivity"

1

Hofmann, Matthias, and Henry F. Schaefer III. "Structure and reactivity of the vinylcyclopropane radical cation." Journal of Molecular Structure 599, no. 1-3 (2001): 95–116. http://dx.doi.org/10.1016/s0022-2860(01)00848-1.

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Li, Miao‐Miao, Qin Xiong, Bao‐Le Qu, et al. "Utilizing Vinylcyclopropane Reactivity: Palladium‐Catalyzed Asymmetric [5+2] Dipolar Cycloadditions." Angewandte Chemie 132, no. 40 (2020): 17582–87. http://dx.doi.org/10.1002/ange.202006366.

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Li, Miao‐Miao, Qin Xiong, Bao‐Le Qu, et al. "Utilizing Vinylcyclopropane Reactivity: Palladium‐Catalyzed Asymmetric [5+2] Dipolar Cycloadditions." Angewandte Chemie International Edition 59, no. 40 (2020): 17429–34. http://dx.doi.org/10.1002/anie.202006366.

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4

Herbertz, Torsten, and Heinz D. Roth. "Structure and Reactivity of Vinylcyclopropane Radical Cation: Electron Transfer Photochemistry andab InitioCalculations." Journal of the American Chemical Society 120, no. 46 (1998): 11904–11. http://dx.doi.org/10.1021/ja980367s.

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5

Schoerpf, Sebastian, Yohann Catel, Norbert Moszner, Christian Gorsche, and Robert Liska. "Enhanced reduction of polymerization-induced shrinkage stress via combination of radical ring opening and addition fragmentation chain transfer." Polymer Chemistry 10, no. 11 (2019): 1357–66. http://dx.doi.org/10.1039/c8py01540f.

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The combination of vinylcyclopropanes with an ester-activated vinyl sulfonate ester in a light-induced radical polymerization shows high reactivity accompanied by a significant increase in conversion and it leads to an enhanced reduction of polymerization-induced shrinkage stress.
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6

Chandrasekaran, Srinivasan, and Venkataraman Ganesh. "Recent Advances in the Synthesis and Reactivity of Vinylcyclopropanes." Synthesis 48, no. 24 (2016): 4347–80. http://dx.doi.org/10.1055/s-0035-1562530.

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7

Scuiller, Anaïs, Alexandre Karnat, Nicolas Casaretto, and Alexis Archambeau. "Vinylcyclopropanes as All-Carbon 1,5-Dipoles: A Reactivity Switch for Palladium-Catalyzed (5 + 4) Cycloadditions." Organic Letters 23, no. 6 (2021): 2332–36. http://dx.doi.org/10.1021/acs.orglett.1c00477.

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Pandey, Rajesh K., Lizhu Wang, Nathaniel J. Wallock, Sergey Lindeman, and William A. Donaldson. "Reactivity of (2-Alkenyl-3-pentene-1,5-diyl)iron Complexes: Preparation of Functionalized Vinylcyclopropanes and Cycloheptadienes." Journal of Organic Chemistry 73, no. 18 (2008): 7236–45. http://dx.doi.org/10.1021/jo801446q.

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9

Liu, Peng, Paul†Ha-Yeon Cheong, Zhi-Xiang Yu, Paul A Wender, and Kendall N Houk. "Substituent Effects, Reactant Preorganization, and Ligand Exchange Control the Reactivity in RhI-Catalyzed (5+2) Cycloadditions between Vinylcyclopropanes and Alkynes." Angewandte Chemie International Edition 47, no. 21 (2008): 3939–41. http://dx.doi.org/10.1002/anie.200800420.

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10

Liu, Peng, Paul Ha-Yeon Cheong, Zhi-Xiang Yu, Paul A Wender, and Kendall N Houk. "Substituent Effects, Reactant Preorganization, and Ligand Exchange Control the Reactivity in RhI-Catalyzed (5+2) Cycloadditions between Vinylcyclopropanes and Alkynes." Angewandte Chemie 120, no. 21 (2008): 4003–5. http://dx.doi.org/10.1002/ange.200800420.

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Dissertations / Theses on the topic "Vinylcyclopropane Reactivity"

1

Ganesh, V. "Studies On the Ring-Opening Reaftions Of Vinylcyclopropanes, Vinylcyclobutanes And Other Snmall-Ring Systems." Thesis, 2012. http://etd.iisc.ac.in/handle/2005/3237.

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The thesis entitled “Studies on the Ring-opening Reactions of Vinylcyclopropanes, Vinylcyclobutanes, and other Small-ring Systems” is divided into four chapters. Chapter 1: Part A: Bromenium Catalyzed Tandem Ring-opening/Cyclization of Vinylcyclopropanes and Vinylcyclobutanes: A [3+2+1]/[4+2+1] Cascade for the Synthesis of Chiral Amidines. In this part of the Chapter, we discuss our serendipitous results in the reaction of vinylcyclopropanes (VCPs), like Δ2-carene under Sharpless aziridination conditions using chloramine-T and phenyltrimethylammonium tribromide (PTAB) as catalyst in acetonit
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2

Ganesh, V. "Studies On the Ring-Opening Reaftions Of Vinylcyclopropanes, Vinylcyclobutanes And Other Snmall-Ring Systems." Thesis, 2012. http://hdl.handle.net/2005/3237.

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Abstract:
The thesis entitled “Studies on the Ring-opening Reactions of Vinylcyclopropanes, Vinylcyclobutanes, and other Small-ring Systems” is divided into four chapters. Chapter 1: Part A: Bromenium Catalyzed Tandem Ring-opening/Cyclization of Vinylcyclopropanes and Vinylcyclobutanes: A [3+2+1]/[4+2+1] Cascade for the Synthesis of Chiral Amidines. In this part of the Chapter, we discuss our serendipitous results in the reaction of vinylcyclopropanes (VCPs), like Δ2-carene under Sharpless aziridination conditions using chloramine-T and phenyltrimethylammonium tribromide (PTAB) as catalyst in acetonit
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