Literatura académica sobre el tema "Fluorocyclopropane"
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Artículos de revistas sobre el tema "Fluorocyclopropane"
Dall'O, L. y H. Heydtmann. "Kinetic Study of Chemically Activated Fluorocyclopropane". Berichte der Bunsengesellschaft für physikalische Chemie 91, n.º 1 (enero de 1987): 24–30. http://dx.doi.org/10.1002/bbpc.19870910107.
Texto completoToyota, Akemi, Yoshinori Ono, Chikara Kaneko y Isao Hayakawa. "A novel stereoselective synthesis of cis-2-fluorocyclopropane-1-carboxylic acid". Tetrahedron Letters 37, n.º 47 (noviembre de 1996): 8507–10. http://dx.doi.org/10.1016/0040-4039(96)01952-1.
Texto completoTOYOTA, A., Y. ONO, C. KANEKO y I. HAYAKAWA. "ChemInform Abstract: A Novel Stereoselective Synthesis of cis-2-Fluorocyclopropane-1- carboxylic Acid." ChemInform 28, n.º 12 (4 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199712078.
Texto completoPons, 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, n.º 6 (4 de febrero de 2022): 4868–78. http://dx.doi.org/10.1021/acsomega.1c05337.
Texto completoKaupert, Cornelia, Horst Heydtmann y Walter Thiel. "The vibrational spectra of the monohalogenated cyclopropanes: Ab initio calculations and an experimental study of fluorocyclopropane". Chemical Physics 156, n.º 1 (septiembre de 1991): 85–93. http://dx.doi.org/10.1016/0301-0104(91)87040-3.
Texto completoZhang, Fei, Zhiguo J. Song, Dave Tschaen y R. P. Volante. "Enantioselective Preparation of Ring-Fused 1-Fluorocyclopropane-1-carboxylate Derivatives: En Route to mGluR 2 Receptor Agonist MGS0028". Organic Letters 6, n.º 21 (octubre de 2004): 3775–77. http://dx.doi.org/10.1021/ol0484512.
Texto completoSaito, Akio, Hisanaka Ito y 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, n.º 35 (agosto de 2001): 7487–93. http://dx.doi.org/10.1016/s0040-4020(01)00726-8.
Texto completoDelion, Laëtitia, Thomas Poisson, Philippe Jubault, Xavier Pannecoucke y André B. Charette. "Synthesis of fluorocyclopropanes via the enantioselective cyclopropanation of fluoro-substituted allylic alcohols using zinc carbenoids". Canadian Journal of Chemistry 98, n.º 9 (septiembre de 2020): 516–23. http://dx.doi.org/10.1139/cjc-2020-0036.
Texto completoSaito, Akio, Hisanaka Ito y 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, n.º 51 (23 de mayo de 2010): no. http://dx.doi.org/10.1002/chin.200151053.
Texto completoGarbacz, Piotr, Janusz Cukras y Michał Jaszuński. "A theoretical study of potentially observable chirality-sensitive NMR effects in molecules". Physical Chemistry Chemical Physics 17, n.º 35 (2015): 22642–51. http://dx.doi.org/10.1039/c5cp02870a.
Texto completoTesis sobre el tema "Fluorocyclopropane"
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.
Texto completoFluorine 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
Shelton, G. Robert. "Computational investigation of 1-fluorocyclopropenes". [Gainesville, Fla.] : University of Florida, 2004. http://purl.fcla.edu/fcla/etd/UFE0007541.
Texto completoCapítulos de libros sobre el tema "Fluorocyclopropane"
"Product Class 2: Fluorocyclopropanes". En Category 5, Compounds with One Carbon Heteroatom Bond, editado por Percy. Stuttgart: Georg Thieme Verlag, 2006. http://dx.doi.org/10.1055/sos-sd-034-00152.
Texto completo"34.2.2 Fluorocyclopropanes (Update 2017)". En Knowledge Updates: 2017/2, editado por Christmann, Paquin, Weinreb, Carreira y Schaumann. Stuttgart: Georg Thieme Verlag, 2017. http://dx.doi.org/10.1055/sos-sd-134-00144.
Texto completoKawase, T. "From 1-Bromo-1-fluorocyclopropanes". En Cumulenes and Allenes, 1. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-044-00316.
Texto completoChallenger, S. "Synthesis of 1-Chloro-1-fluorocyclopropanes". En 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.
Texto completoChallenger, S. "Synthesis of 1-Bromo-1-fluorocyclopropanes". En 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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