By Norbert Baumann, Hans-Jürgen Fachmann, Brigitte Heibel, Reimund Jotter, Birgit Ledüc, Alfons Kubny, U. Hettwer, R. Bohrer, U. Nohl, H.-J. Richter-Ditten
PF3, (CH3)3SiCl -> (CH3)3SiF, and RC(O)Cl -> RC(O)F. Others contain the conversion of (C6H5)3P into (C6H5)3PF2 and of (R3NC(S)S)2 into R2NCF3, R=alkyl. In natural chemistry, fluorides are simply available from alcohols, geminal fluorides RR'CF2 from the respective aldehydes or ketones, and acyl fluorides RC(O)F from carboxylic acides through the use of DAST. simply because DAST is straightforward to address and offers fresh reactions in syntheses, this Gmelin quantity devotes a lot area to the outline of the chemical and actual houses od DAST.
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Additional resources for S Sulfur-Nitrogen Compounds Part 8: Compounds with Sulfur of Oxidation Number IV
Ber. 112  2158/66). ; Boivin, J. L. (Can. J. Chern. 42  1759/60). ; Sunderrneyer, W. (J. Fluorine Chern. 18  259/68).  Griffiths, J. E; Sturman, D. F. (Spectrochirn. Acta A 25  1355/62).  Vorob'ev, M. ; Filatov, A. ; Englin, M. A. (Zh. Obshch. Khirn. 43  1653; J. Gen. Chern. [USSR] 43  1638).  Vorob'ev, M. ; Filatov, A. ; Englin, M. A. (Zh. Obshch. Khirn. 42  1942/4; J. Gen. Chern. [USSR] 42  193517).  Srnith, W. C. S. A. 19599152). ; Biermann, U.
Chem. 14 1859/61). ; Ahlrichs, R. (Chem. Phys. 108  429/39). Lustig, M. (private communication from Horn, H. , Fluorine Chem. Rev. 6 135/92). Zaborowski, L. ; Shreeve, J. M. (J. Am. Chem. Soc. 92 3665/8). ; Carr, D. T. (J. Phys. Chem. 67 112/5). ; Sundermeyer, W. (J. Fluorine Chem. 18  259/68). ; Fox, W. ; De Marco, R. ; Moniz, W. B. (J. Magn. Resonance 34  295/9).  Griffiths, J. ; Sturman, D. F. (Spectrochim. Acta A 25 1355/62).  Larson, J.
Z. Naturforsch. 22b  550). ; Alange, G. G. (Israel J. Chem. 17 137/40). ; Glemser, O. (Z. Naturforsch. 32b 160/2). ; Mews, R. (Chem. Ber. 114 1539/41). 5 Tellurium-Substituted Imidosulturous DIfluoride N-(Pentafluoro-l6-tellanyl)-imidosulfurous Ditluorlde, F2S=NTeF5 The compound was prepared by stirring a mixture of (CH 3hSiNHTeF5 and SF4 (mole ratio -2:1) overnight at room temperature. Slow vacuum distiUation gave the titte compound in 40% yield. p. -78°C. 2 (SF2), AB4X2type; 2J(FA, FB) =177, 4J(FA,SF2) = 14, 3J(125Te, SF2) = 329, lJ(l25Te, FA) = 3438, lJ(l25Te, FB) =3624 Hz.