Organofluorchemie (Dutch Wikipedia)

Analysis of information sources in references of the Wikipedia article "Organofluorchemie" in Dutch language version.

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17doi.org

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acs.org

pubs.acs.org

Ann M. Thayer “Fabulous Fluorine” Chemical and Engineering News, June 5, 2006, Volume 84, pp. 15-24. http://pubs.acs.org/cen/coverstory/84/8423cover1.html

archive.org

C. Heidelberger, N. K. Chaudhuri, P. Danneberg, D. Mooren, L. Griesbach, R. Duschinsky, R. J. Schnitzer, E. Pleven, and J. Schreiner (1957). Fluorinated Pyrimidines, A New Class of Tumour-Inhibitory Compounds. Nature 179 (4561): 663. PMID 13418758. DOI: 10.1038/179663a0.

doi.org

William R. Dolbier, Jr. (2005). Fluorine Chemistry at the Millennium. Journal of Fluorine Chemistry 126: 157. DOI: 10.1016/j.jfluchem.2004.09.033.
C. Heidelberger, N. K. Chaudhuri, P. Danneberg, D. Mooren, L. Griesbach, R. Duschinsky, R. J. Schnitzer, E. Pleven, and J. Schreiner (1957). Fluorinated Pyrimidines, A New Class of Tumour-Inhibitory Compounds. Nature 179 (4561): 663. PMID 13418758. DOI: 10.1038/179663a0.
O'Hagan, D, Schaffrath, C, Cobb, S. L (2002). Biochemistry: biosynthesis of an organofluorine molecule. Nature. 416 (6878): 279. PMID 11907567. DOI: 10.1038/416279a.
J. Lapasset, J. Moret, M. Melas, A. Collet, M. Viguier, H. Blancou (1996). Crystal structure of 12,12,13,13,14,14,15,15,16,16,17,17,17-tridecafluoroheptadecan-1-ol, C₁₇H₂₃F₁₃O. Z. Kristallogr. 211: 945. DOI: 10.1524/zkri.1996.211.12.945. CSD entry TULQOG.
C.E. Smith, P.S. Smith, R.Ll. Thomas, E.G. Robins, J.C. Collings, Chaoyang Dai, A.J. Scott, S. Borwick, A.S. Batsanov, S.W. Watt, S.J. Clark, C. Viney, J.A.K. Howard, W. Clegg, T.B. Marder (2004). Arene-perfluoroarene interactions in crystal engineering: structural preferences in polyfluorinated tolans. J. Mater. Chem. 14: 413. DOI: 10.1039/b314094f. CSD entry ASIJIV.
Dana Lyn S. Brahms, and William P. Dailey (1996). Fluorinated Carbenes. Chemical Reviews 96 (5): 1585–1632. PMID 11848805. DOI: 10.1021/cr941141k.
Brunet, Vincent A., O'Hagan, David (2008). Catalytic Asymmetric Fluorination Comes of Age. Angewandte Chemie, International Edition 47 (7): 1179–1182. PMID 18161722. DOI: 10.1002/anie.200704700.
Stéphane Caron, Robert W. Dugger, Sally Gut Ruggeri, John A. Ragan, and David H. Brown Ripin (2006). Large-Scale Oxidations in the Pharmaceutical Industry. Chemical Reviews 106 (7): 2943–2989. PMID 16836305. DOI: 10.1021/cr040679f.
Gauri S. Lal, Guido P. Pez, Reno J. Pesaresi and Frank M. Prozonic (1999). Bis(2-methoxyethyl)aminosulfur trifluoride: a new broad-spectrum deoxofluorinating agent with enhanced thermal stability. Chemical Communications: 215. DOI: 10.1039/a808517j.
Le Bars, D. (2006). Fluorine-18 and Medical Imaging: Radiopharmaceuticals for Positron Emission Tomography. Journal of Fluorine Chemistry 127: 1488–1493. DOI: 10.1016/j.jfluchem.2006.09.015. .
O'Hagan, D (1999). Fluorine-Containing Natural Products. Journal of Fluorine Chemistry 100: 127–133. DOI: 10.1016/S0022-1139(99)00201-8.

dx.doi.org

G. Siegemund, W. Schwertfeger, A. Feiring, B. Smart, F. Behr, H. Vogel, B. McKusick “Fluorine Compounds, Organic” in “Ullmann’s Encyclopedia of Industrial Chemistry” 2005, Wiley-VCH, Weinheim. DOI:10.1002/14356007.a11 349
J.H. Simons – The Electrochemical Process for the Production of Fluorocarbons, Journal of The Electrochemical Society, 1949, Volume 95, pp. 47-66. DOI: doi:10.1149/1.2776733
E.G. Hopea, A.P. Abbotta, D.L. Daviesa, G.A. Solana and A.M. Stuarta “Green Organometallic Chemistry” in Comprehensive Organometallic Chemistry III, 2007, Volume 12, Pages 837-864. DOI:10.1016/B0-08-045047-4/00182-5
M.E. Thompson, P.E. Djurovich, S. Barlow and S. Marder “Organometallic Complexes for Optoelectronic Applications” Comprehensive Organometallic Chemistry III, 2007, Volume 12, Pages 101-194. DOI:10.1016/B0-08-045047-4/00169-2
J.C. Peters, J.C. Thomas “Ligands, Reagents, and Methods in Organometallic Synthesis” in Comprehensive Organometallic Chemistry III, 2007, Volume 1, Pages 59-92. DOI:10.1016/B0-08-045047-4/00002-9
R.N. Perutz and T. Braun “Transition Metal-mediated C–F Bond Activation” Comprehensive Organometallic Chemistry III, 2007, Volume 1, Pages 725-758. DOI:10.1016/B0-08-045047-4/00028-5.

nih.gov

ncbi.nlm.nih.gov

C. Heidelberger, N. K. Chaudhuri, P. Danneberg, D. Mooren, L. Griesbach, R. Duschinsky, R. J. Schnitzer, E. Pleven, and J. Schreiner (1957). Fluorinated Pyrimidines, A New Class of Tumour-Inhibitory Compounds. Nature 179 (4561): 663. PMID 13418758. DOI: 10.1038/179663a0.
O'Hagan, D, Schaffrath, C, Cobb, S. L (2002). Biochemistry: biosynthesis of an organofluorine molecule. Nature. 416 (6878): 279. PMID 11907567. DOI: 10.1038/416279a.
Dana Lyn S. Brahms, and William P. Dailey (1996). Fluorinated Carbenes. Chemical Reviews 96 (5): 1585–1632. PMID 11848805. DOI: 10.1021/cr941141k.
Brunet, Vincent A., O'Hagan, David (2008). Catalytic Asymmetric Fluorination Comes of Age. Angewandte Chemie, International Edition 47 (7): 1179–1182. PMID 18161722. DOI: 10.1002/anie.200704700.
Stéphane Caron, Robert W. Dugger, Sally Gut Ruggeri, John A. Ragan, and David H. Brown Ripin (2006). Large-Scale Oxidations in the Pharmaceutical Industry. Chemical Reviews 106 (7): 2943–2989. PMID 16836305. DOI: 10.1021/cr040679f.

orgsyn.org

(en) A.I. Vogel, J. Leicester, W.A.T. Macey (1963) – n-Hexyl Fluoride, Organic Syntheses, 4, p. 525
(en) D.T. Flood (1943) – Fluorobenzene, Organic Syntheses, 2, p. 295
(en) P. Ramaiah, R. Krishnamurti & G.K.S. Prakash (1998) – 1-(trifluoromethyl)-1-cyclohexanol, Organic Syntheses, 9, p. 232
(en) K.S. Ravikumar, V. Kesavan, B. Crousse, D. Bonnet-Delpon & J.-P. Bégué (2003) – Mild and Selective Oxidation of Sulfur Compounds in Trifluorethanol: Diphenyl Disulfide and Methyle Phenyl Sulfoxide, Organic Syntheses, 80, p. 184
(en) A. Crombie, S.-Y. Kim, S. Hadida & D.P. Curran (2004) – Synthesis of Tris(2-Perfluorohexylethyl)tin Hydride: A Highly Fluorinated Tin Hydride with Advantageous Features of Easy Purification, Organic Syntheses, 10, p. 712

web.archive.org

Roy J. Plunkett Chemical Heritage Foundation. Retrieved 10 September 2006.