Synlett 2015; 26(01): 33-35
DOI: 10.1055/s-0034-1379721
cluster
© Georg Thieme Verlag Stuttgart · New York

Cluster Preface: Progress in Organo-Fluorine Chemistry

Duncan L. Browne*
School of Chemistry, Cardiff University, Main Building, Park Place, Cardiff, CF10 3AT, UK   eMail: DLBrowne@cardiff.ac.uk
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Publikationsverlauf

Received: 30. September 2014

Accepted: 01. Oktober 2014

Publikationsdatum:
16. Dezember 2014 (online)


Abstract

The chance of achieving a successful ‘hit’ in the search for new and improved functional organic molecules can be increased by appropriate fluorination. To this end, many new and exciting methods for the site-selective, controlled fluorination of organic molecules are being developed. This Cluster contains a series of articles that represent the most recent achievements in this field.

 
  • References

    • 1a Kirsch P. Modern Fluoroorganic Chemistry. 2nd ed. Wiley-VCH; Weinheim: 2013
    • 1b Liang T, Neumann CN, Ritter T. Angew. Chem. Int. Ed. 2013; 52: 8214
    • 1c O’Hagan D. Chem. Soc. Rev. 2008; 37: 308
    • 2a Kirk KL. J. Fluorine Chem. 2006; 127: 1013
    • 2b Purser S, Moore PR, Swallow S, Gouverneur V. Chem. Soc. Rev. 2008; 37: 320
    • 2c Jeschke P. ChemBioChem 2004; 5: 570
    • 3a Böhm HJ, Banner D, Bendels S, Kansy M, Kuhn B, Müller K, Obst-Sander U, Stahl M. ChemBioChem 2004; 5: 637
    • 3b Müller K, Faeh C, Diederich F. Science 2007; 317: 1881
    • 3c Morgenthaler M, Schweizer E, Hoffmann-Röder A, Benini F, Martin RE, Jaeschke G, Wagner B, Fischer H, Bendels S, Zimmerli D, Schneider J, Diederich F, Kansy M, Müller K. ChemMedChem 2007; 2: 1100
  • 4 Miller PW, Long NJ, Vilar R, Gee AD. Angew. Chem. Int. Ed. 2008; 47: 8998
  • 5 Ruiz-Cabello J, Barnett BP, Bottomley PA, Bulte JW. M. NMR Biomed. 2011; 24: 114
    • 6a Sparr C, Schweizer WB, Senn HM, Gilmour R. Angew. Chem. Int. Ed. 2009; 48: 3065
    • 6b For an overview of the influence of fluorine in asymmetric catalysis, see: Cahard C, Bizet V. Chem. Soc. Rev. 2014; 43: 135
  • 7 Lv J, Zhang L, Hu S, Cheng J.-P, Luo S. Chem. Eur. J. 2012; 18: 799
  • 8 Markovskij LN, Pashinnik VE, Kirsanov AV. Synthesis 1973; 787
  • 9 Umemoto T, Tomita K. Tetrahedron Lett. 1986; 27: 3271
    • 10a Ruppert I, Schlich K, Volbach W. Tetrahedron Lett. 1984; 25: 2195
    • 10b Prakash GK. S, Krishnamurti R, Olah GA. J. Am. Chem. Soc. 1989; 111: 393
    • 11a Yagupolskii LM, Kondratenko NV, Temofeeva GN. J. Org. Chem. USSR 1984; 20: 103
    • 11b Umemoto T, Ishihara S. Tetrahedron Lett. 1990; 31: 3579
    • 12a Barnette WE. J. Am. Chem. Soc. 1984; 106: 452
    • 12b Singh S, DesMarteau DD, Zuberi SS, Witz M, Huang HN. J. Am. Chem. Soc. 1987; 109: 7194
    • 12c Differding E, Ofner H. Synlett 1991; 187
  • 13 Banks RE, Mohialdin-Khaffaf SN, Lal GS, Shariff I, Syvret RG. J. Chem. Soc., Chem. Commun. 1992; 595
  • 14 Lal GS, Pez GP, Pesaresi RJ, Prozonic FM. Chem. Commun. 1999; 215
  • 15 Eisenberger P, Gischig S, Togni A. Chem. Eur. J. 2006; 12: 2579
  • 16 Beaulieu F, Beauregard L.-P, Courchesne G, Courturier M, LaFlamme F, L’Heureux A. Org. Lett. 2009; 11: 5050
  • 17 Umemoto T, Singh RP, Xu Y, Saito N. J. Am. Chem. Soc. 2010; 132: 18199
  • 18 Tang P, Wang W, Ritter T. J. Am. Chem. Soc. 2011; 133: 11482
  • 19 Fujiwara Y, Dixon JA, Rodriguez RA, Baxter RD, Dixon DD, Collins MR, Blackmond DG, Baran PS. J. Am. Chem. Soc. 2012; 134: 1494
    • 20a Nagib DA, Scott ME, MacMillan DW. C. J. Am. Chem. Soc. 2009; 131: 10875
    • 20b Nagib DA, MacMillan DW. C. Nature 2011; 480: 224
    • 20c Ye Y, Sanford MS. J. Am. Chem. Soc. 2012; 134: 9034
    • 21a Lie W, Huang X, Cheng M.-J, Nielsen RJ, Goddard III WA, Groves JT. Science 2012; 337: 1322
    • 21b Fujiwara Y, Dixon JA, O’Hara F, Funder ED, Dixon DD, Rodriquez RA, Baxter RD, Herlé B, Sach N, Collins MR, Ishihara Y, Baran PS. Nature 2012; 492: 95
  • 22 Zhang B, Studer A. Org. Lett. 2014; 16: 1216
    • 23a Straathof NJ. W, Gemoets HP. L, Wang X, Schouten JC, Hessel V, Noël T. ChemSusChem 2014; 7: 1612
    • 23b Cantillo D, deFrutos O, Rincon JA, Mateos C, Kappe CO. J. Org. Chem. 2014; 79: 8486
    • 24a Nielsen MC, Bonney KJ, Schoenebeck F. Angew. Chem. Int. Ed. 2014; 53: 5903
    • 24b Anstaett P, Schoenebeck F. Chem. Eur. J. 2011; 17: 12340
    • 24c Grushin V, Marshall WJ. J. Am. Chem. Soc. 2006; 128: 12644