How trimethyl(trifluoromethyl)silane reacts with itself in the presence of naked fluoride-a one-pot synthesis of bis([15]crown-5)cesium 1,1,1,3,5,5,5-heptafluoro-2,4-bis(trifluoromethyl)pentenide

Tyrra W, Kremlev MM, Naumann D, Scherer H, Schmidt H, Hoge B, Pantenburg I, Yagupolskii YL (2005)
CHEMISTRY-A EUROPEAN JOURNAL 11(22): 6514-6518.

Zeitschriftenaufsatz | Veröffentlicht | Englisch
 
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Autor*in
Tyrra, W; Kremlev, MM; Naumann, D; Scherer, H; Schmidt, H; Hoge, BertholdUniBi; Pantenburg, I; Yagupolskii, YL
Erscheinungsjahr
2005
Zeitschriftentitel
CHEMISTRY-A EUROPEAN JOURNAL
Band
11
Ausgabe
22
Seite(n)
6514-6518
ISSN
0947-6539
eISSN
1521-3765
Page URI
https://pub.uni-bielefeld.de/record/2341681

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Tyrra W, Kremlev MM, Naumann D, et al. How trimethyl(trifluoromethyl)silane reacts with itself in the presence of naked fluoride-a one-pot synthesis of bis([15]crown-5)cesium 1,1,1,3,5,5,5-heptafluoro-2,4-bis(trifluoromethyl)pentenide. CHEMISTRY-A EUROPEAN JOURNAL. 2005;11(22):6514-6518.
Tyrra, W., Kremlev, M. M., Naumann, D., Scherer, H., Schmidt, H., Hoge, B., Pantenburg, I., et al. (2005). How trimethyl(trifluoromethyl)silane reacts with itself in the presence of naked fluoride-a one-pot synthesis of bis([15]crown-5)cesium 1,1,1,3,5,5,5-heptafluoro-2,4-bis(trifluoromethyl)pentenide. CHEMISTRY-A EUROPEAN JOURNAL, 11(22), 6514-6518. https://doi.org/10.1002/chem.200500799
Tyrra, W, Kremlev, MM, Naumann, D, Scherer, H, Schmidt, H, Hoge, Berthold, Pantenburg, I, and Yagupolskii, YL. 2005. “How trimethyl(trifluoromethyl)silane reacts with itself in the presence of naked fluoride-a one-pot synthesis of bis([15]crown-5)cesium 1,1,1,3,5,5,5-heptafluoro-2,4-bis(trifluoromethyl)pentenide”. CHEMISTRY-A EUROPEAN JOURNAL 11 (22): 6514-6518.
Tyrra, W., Kremlev, M. M., Naumann, D., Scherer, H., Schmidt, H., Hoge, B., Pantenburg, I., and Yagupolskii, Y. L. (2005). How trimethyl(trifluoromethyl)silane reacts with itself in the presence of naked fluoride-a one-pot synthesis of bis([15]crown-5)cesium 1,1,1,3,5,5,5-heptafluoro-2,4-bis(trifluoromethyl)pentenide. CHEMISTRY-A EUROPEAN JOURNAL 11, 6514-6518.
Tyrra, W., et al., 2005. How trimethyl(trifluoromethyl)silane reacts with itself in the presence of naked fluoride-a one-pot synthesis of bis([15]crown-5)cesium 1,1,1,3,5,5,5-heptafluoro-2,4-bis(trifluoromethyl)pentenide. CHEMISTRY-A EUROPEAN JOURNAL, 11(22), p 6514-6518.
W. Tyrra, et al., “How trimethyl(trifluoromethyl)silane reacts with itself in the presence of naked fluoride-a one-pot synthesis of bis([15]crown-5)cesium 1,1,1,3,5,5,5-heptafluoro-2,4-bis(trifluoromethyl)pentenide”, CHEMISTRY-A EUROPEAN JOURNAL, vol. 11, 2005, pp. 6514-6518.
Tyrra, W., Kremlev, M.M., Naumann, D., Scherer, H., Schmidt, H., Hoge, B., Pantenburg, I., Yagupolskii, Y.L.: How trimethyl(trifluoromethyl)silane reacts with itself in the presence of naked fluoride-a one-pot synthesis of bis([15]crown-5)cesium 1,1,1,3,5,5,5-heptafluoro-2,4-bis(trifluoromethyl)pentenide. CHEMISTRY-A EUROPEAN JOURNAL. 11, 6514-6518 (2005).
Tyrra, W, Kremlev, MM, Naumann, D, Scherer, H, Schmidt, H, Hoge, Berthold, Pantenburg, I, and Yagupolskii, YL. “How trimethyl(trifluoromethyl)silane reacts with itself in the presence of naked fluoride-a one-pot synthesis of bis([15]crown-5)cesium 1,1,1,3,5,5,5-heptafluoro-2,4-bis(trifluoromethyl)pentenide”. CHEMISTRY-A EUROPEAN JOURNAL 11.22 (2005): 6514-6518.

4 Zitationen in Europe PMC

Daten bereitgestellt von Europe PubMed Central.

Palladium-Catalyzed Decarbonylative Trifluoromethylation of Acid Fluorides.
Keaveney ST, Schoenebeck F., Angew Chem Int Ed Engl 57(15), 2018
PMID: 29479784
Anion-Initiated Trifluoromethylation by TMSCF3: Deconvolution of the Siliconate-Carbanion Dichotomy by Stopped-Flow NMR/IR.
Johnston CP, West TH, Dooley RE, Reid M, Jones AB, King EJ, Leach AG, Lloyd-Jones GC., J Am Chem Soc 140(35), 2018
PMID: 30080973
The Role of Ate Complexes in the Copper-Mediated Trifluoromethylation of Alkynes.
Weske S, Schoop R, Koszinowski K., Chemistry 22(32), 2016
PMID: 27385188
Gold trifluoromethyl complexes.
Gil-Rubio J, Vicente J., Dalton Trans 44(45), 2015
PMID: 26169553

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