Academic literature on the topic 'Hydrohydrazination'

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Journal articles on the topic "Hydrohydrazination"

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Zhang, Ming-Xia, Wen-Zuo Li, Hong-Liang Xu, Zi-Yan Zhou, and Shu-Ping Zhuo. "External electric field: a new catalytic strategy for the anti-Markovnikov hydrohydrazination of parent hydrazine." RSC Advances 11, no. 19 (2021): 11595–605. http://dx.doi.org/10.1039/d1ra01037a.

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The anti-Markovnikov hydrohydrazination of parent hydrazine were catalyzed by external electric field (EEF) to a large extent. Furthermore, the solvent effects and the substituent effects of the hydrohydrazination were enhanced in the presence of EEF.
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Liu, Xiangyu, Heng Song, Xiaofang Zhai, Chen-Ho Tung, and Wenguang Wang. "Cobalt-catalyzed regioselective hydrohydrazination of epoxides." Organic & Biomolecular Chemistry 18, no. 8 (2020): 1572–76. http://dx.doi.org/10.1039/d0ob00037j.

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Schweizer, Peter D., Hubert Wadepohl, and Lutz H. Gade. "Titanium-Catalyzed Hydrohydrazination of Carbodiimides." Organometallics 32, no. 13 (2013): 3697–709. http://dx.doi.org/10.1021/om400323p.

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Lukin, Alexey, Tatiana Vedekhina, Dmitry Tovpeko, Nikolay Zhurilo, and Mikhail Krasavin. "Zn-catalyzed hydrohydrazination of propargylamides with BocNHNH2: a novel entry into the 1,2,4-triazine core." RSC Advances 6, no. 63 (2016): 57956–59. http://dx.doi.org/10.1039/c6ra12664b.

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Hydrohydrazination of propargylamides with BocNHNH<sub>2</sub> under Zn(OTf)<sub>2</sub> catalysis gave dihydro-1,2,4-triazines which can be efficiently aromatized in situ with K<sub>3</sub>[Fe(CN)<sub>6</sub>]. This provides a new entry into the medicinally important 1,2,4-triazine core.
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Carreira, E., J. Waser, B. Gaspar, and H. Nambu. "Co-Catalyzed Hydrohydrazination and Hydroazidation of Olefins." Synfacts 2006, no. 11 (2006): 1155. http://dx.doi.org/10.1055/s-2006-949489.

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Alex, Karolin, Annegret Tillack, Nicolle Schwarz, and Matthias Beller. "Zinc-Catalyzed Synthesis of Pyrazolines and Pyrazoles via Hydrohydrazination." Organic Letters 10, no. 12 (2008): 2377–79. http://dx.doi.org/10.1021/ol800592s.

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Hunt, Ashley D., Isabelle Dion, Nicolas Das Neves, Sandrine Taing, and André M. Beauchemin. "Synthesis of Azomethine Imines Using an Intramolecular Alkyne Hydrohydrazination Approach." Journal of Organic Chemistry 78, no. 17 (2013): 8847–52. http://dx.doi.org/10.1021/jo4011409.

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Bunker, Kevin D., Neal W. Sach, Qinhua Huang, and Paul F. Richardson. "Scalable Synthesis of 1-Bicyclo[1.1.1]pentylamine via a Hydrohydrazination Reaction." Organic Letters 13, no. 17 (2011): 4746–48. http://dx.doi.org/10.1021/ol201883z.

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Banerjee, Sanjukta, Eyal Barnea, and Aaron L. Odom. "Titanium-Catalyzed Hydrohydrazination with Monosubstituted Hydrazines: Catalyst Design, Synthesis, and Reactivity." Organometallics 27, no. 5 (2008): 1005–14. http://dx.doi.org/10.1021/om700852v.

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Peltier, Jesse L., Rodolphe Jazzar, Mohand Melaimi, and Guy Bertrand. "Ancillary ligand-free copper catalysed hydrohydrazination of terminal alkynes with NH2NH2." Chemical Communications 52, no. 13 (2016): 2733–35. http://dx.doi.org/10.1039/c5cc10427k.

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Dissertations / Theses on the topic "Hydrohydrazination"

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Loiseau, Francis. "Cope-type Hydroamination of Alkenes with Hydroxylamines and Hydrazines - Scope and Mechanism." Thèse, Université d'Ottawa / University of Ottawa, 2013. http://hdl.handle.net/10393/23794.

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Hydroamination stands as a desirable approach to nitrogen-containing molecules, which have important applications ranging from pharmaceuticals (fine chemicals) to paints, coatings, insecticides and agrochemicals (bulk chemicals). It features the use of alkene and alkyne starting materials, which are abundant and rarely used in the formation of C-N bonds. This work aims at building on the improved Cope-type reactivity developed in the Beauchemin group by expanding the reach of the reaction and understanding its mechanistic complexities. The first part of this thesis describes the development of
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