Academic literature on the topic 'Fluorocyclopropane'

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Journal articles on the topic "Fluorocyclopropane":

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Dall'O, L., and H. Heydtmann. "Kinetic Study of Chemically Activated Fluorocyclopropane." Berichte der Bunsengesellschaft für physikalische Chemie 91, no. 1 (January 1987): 24–30. http://dx.doi.org/10.1002/bbpc.19870910107.

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Toyota, Akemi, Yoshinori Ono, Chikara Kaneko, and Isao Hayakawa. "A novel stereoselective synthesis of cis-2-fluorocyclopropane-1-carboxylic acid." Tetrahedron Letters 37, no. 47 (November 1996): 8507–10. http://dx.doi.org/10.1016/0040-4039(96)01952-1.

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TOYOTA, A., Y. ONO, C. KANEKO, and I. HAYAKAWA. "ChemInform Abstract: A Novel Stereoselective Synthesis of cis-2-Fluorocyclopropane-1- carboxylic Acid." ChemInform 28, no. 12 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199712078.

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Pons, Amandine, Jonathan Decaens, Riham Najjar, Nansalmaa Otog, Mathieu Arribat, Sandrine Jolly, Samuel Couve-Bonnaire, et al. "Fluorocyclopropane-Containing Proline Analogue: Synthesis and Conformation of an Item in the Peptide Chemistʼs Toolbox." ACS Omega 7, no. 6 (February 4, 2022): 4868–78. http://dx.doi.org/10.1021/acsomega.1c05337.

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Kaupert, Cornelia, Horst Heydtmann, and Walter Thiel. "The vibrational spectra of the monohalogenated cyclopropanes: Ab initio calculations and an experimental study of fluorocyclopropane." Chemical Physics 156, no. 1 (September 1991): 85–93. http://dx.doi.org/10.1016/0301-0104(91)87040-3.

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Zhang, Fei, Zhiguo J. Song, Dave Tschaen, and R. P. Volante. "Enantioselective Preparation of Ring-Fused 1-Fluorocyclopropane-1-carboxylate Derivatives: En Route to mGluR 2 Receptor Agonist MGS0028." Organic Letters 6, no. 21 (October 2004): 3775–77. http://dx.doi.org/10.1021/ol0484512.

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Saito, Akio, Hisanaka Ito, and Takeo Taguchi. "A stereoselective preparation of 1-fluorocyclopropane-1-carboxylate derivatives through radical addition of fluoroiodoacetate to alkenes followed by intramolecular substitution reaction." Tetrahedron 57, no. 35 (August 2001): 7487–93. http://dx.doi.org/10.1016/s0040-4020(01)00726-8.

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Delion, Laëtitia, Thomas Poisson, Philippe Jubault, Xavier Pannecoucke, and André B. Charette. "Synthesis of fluorocyclopropanes via the enantioselective cyclopropanation of fluoro-substituted allylic alcohols using zinc carbenoids." Canadian Journal of Chemistry 98, no. 9 (September 2020): 516–23. http://dx.doi.org/10.1139/cjc-2020-0036.

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Abstract:
Cyclopropanation reactions using zinc carbenoids are a powerful means to access cyclopropanes. Described herein is an enantioselective version of the reaction using zinc reagents and a chiral dioxaborolane ligand in the generation of fluorocyclopropanes. Readily available 2- and 3-fluoroallylic alcohols were efficiently cyclopropanated in high yields and excellent enantioselectivities. This method provides access to a variety of structurally diverse chiral fluorocyclopropanes that can be used as useful chiral building blocks.
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Saito, Akio, Hisanaka Ito, and Takeo Taguchi. "ChemInform Abstract: A Stereoselective Preparation of 1-Fluorocyclopropane-1-carboxylate Derivatives Through Radical Addition of Fluoroiodoacetate to Alkenes Followed by Intramolecular Substitution Reaction." ChemInform 32, no. 51 (May 23, 2010): no. http://dx.doi.org/10.1002/chin.200151053.

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Garbacz, Piotr, Janusz Cukras, and Michał Jaszuński. "A theoretical study of potentially observable chirality-sensitive NMR effects in molecules." Physical Chemistry Chemical Physics 17, no. 35 (2015): 22642–51. http://dx.doi.org/10.1039/c5cp02870a.

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Dissertations / Theses on the topic "Fluorocyclopropane":

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Audet, Florian. "Development of new access routes to fluorinated building blocks for agrochemical applications." Electronic Thesis or Diss., Strasbourg, 2024. http://www.theses.fr/2024STRAF002.

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Abstract:
Le fluor est naturellement présent sur Terre sous forme de sels, notamment de fluorure de calcium. Il est également utilisé pour de nombreuses applications industrielles dont les domaines pharmaceutiques et agrochimiques. En effet, de nombreux principes actifs utilisés dans ces domaines contiennent au moins un atome de fluor ce qui leur confère des propriétés particulières en modulant ses paramètres physico-chimiques et biologiques. L’objectif de cette thèse, en partenariat avec Bayer CropScience, était de développer de nouvelles voies d’accès à des synthons fluorés pour des applications en agrochimie. Nous nous sommes d’abord intéressés à une réaction de couplage croisé d’électrophiles en conditions électrochimiques permettant l’accès au motif difluorométhylène. Des réactions de N-polyfluoroalkylations ont ensuite été développées en utilisant le fluorure de sulfuryle comme réactif clé. Enfin, une réaction de couplage croisé d’un nouveau réactif de type (1-fluorocyclopropyl)metalloïde a été mise au point, permettant l’introduction direct de ce motif fluoré émergent
Fluorine is naturally occurring on Earth in the form of salts, the most notable being calcium fluoride. Over the last decades, has been used in numerous industrial applications, including pharmaceuticals and agrochemicals. Indeed, many active ingredients used in these fields contain at least one fluorine atom, giving them unique properties by modulating their physico-chemical and biological parameters.The objective of this thesis, in partnership with Bayer CropScience, was to develop new ways of accessing fluorinated synthons for agrochemical applications. We started by investigating a cross-electrophile coupling reaction under electrochemical conditions to access the difluoromethylene moiety. N-Polyfluoroalkylation reactions were then developed using sulfuryl fluoride as the key reagent. Finally, a cross-coupling reaction with a new (1-fluorocyclopropyl)metaloid reagent was developed, enabling the direct introduction of this emerging fluorinated group
2

Shelton, G. Robert. "Computational investigation of 1-fluorocyclopropenes." [Gainesville, Fla.] : University of Florida, 2004. http://purl.fcla.edu/fcla/etd/UFE0007541.

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Book chapters on the topic "Fluorocyclopropane":

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"Product Class 2: Fluorocyclopropanes." In Category 5, Compounds with One Carbon Heteroatom Bond, edited by Percy. Stuttgart: Georg Thieme Verlag, 2006. http://dx.doi.org/10.1055/sos-sd-034-00152.

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"34.2.2 Fluorocyclopropanes (Update 2017)." In Knowledge Updates: 2017/2, edited by Christmann, Paquin, Weinreb, Carreira, and Schaumann. Stuttgart: Georg Thieme Verlag, 2017. http://dx.doi.org/10.1055/sos-sd-134-00144.

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Kawase, T. "From 1-Bromo-1-fluorocyclopropanes." In Cumulenes and Allenes, 1. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-044-00316.

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Challenger, S. "Synthesis of 1-Chloro-1-fluorocyclopropanes." In Acetals: Hal/X and O/O, S, Se, Te, 1. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-029-00037.

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Challenger, S. "Synthesis of 1-Bromo-1-fluorocyclopropanes." In Acetals: Hal/X and O/O, S, Se, Te, 1. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-029-00048.

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