3. , 9. , H. Stockwell, and B. R. , 1H, H18) ; 1,63 (s, 3H, H20) ; 1,67 (s, 3H, H21), RMN 1 H (CDCl 3 , 300 MHz) : ? ?0 H3 et H6), pp.091274008427396478-1, 2000.

R. J. Spandl, M. Díaz?gavilán, K. M. Connell, G. L. Thomas, and D. R. Spring, Diversity???oriented synthesis, The Chemical Record, vol.416, issue.3, p.129, 2008.
DOI : 10.2174/1386207003331454

K. C. Nicolaou, Z. Yang, J. J. Liu, H. Ueno, P. G. Nantermet et al., Total synthesis of taxol, Nature, vol.367, issue.6464, p.630, 1994.
DOI : 10.1038/367630a0

K. S. Lam, S. E. Salmon, E. M. Hersh, V. J. Hruby, W. M. Kazmierski et al., (13) Briganti, S.; Camera, E.; Picardo, M. Pigment Cell Res, Org. Biomol. Chem. Cent. Eur. J. Public Health Tox. Pharm. Phytother. Res. Pure Appl. Chem. Int. J. Mol. Sci. J.; Uyama, H. Cell. Mol.r Life Sci J. Agric. Food Chem. Nat. Prod. Rep. Bioorganic Med. Chem. Lett. Noh, J. M.; Kwak, S. Y.; Kim, D. H.; Lee, Y. S. Biopolymers J. Organomet. Chem. Arch. Pharm. Chem. Life Sci, vol.354, issue.339, pp.82-98, 1149.

K. Kanno, E. Igarashi, Y. Mizukami, K. Nakajima, Z. Song et al., Elaboration de librairies de molécules structurellement diversifiées à partir du squelette de l'acide kojique par des méthodes de synthèse micro­ondes et de flux continu (70) McBride, Tetrahedron J. Am. Chem. Soc. Tetrahedron Lett. Can. J. Chem. J. J. Chem. Soc. Chem. Commun. J. Chem. Soc. Perkin Trans. 1 J. Org. Chem. Acta Chem. Scand. Tetrahedron J. Org. Chem. J. Am. Chem. Soc. Wender, P.; Mascarenas, J. J. Org. Chem. Tetrahedron Lett. J. Am. Chem. Soc. J. Am. Chem. Soc. J. Org. Chem. Tetrahedron Lett. Tetrahedron J. Org. Chem. J. Org. Chem. J. L. Tetrahedron Lett. J. Org. Chem. Tetrahedron Lett. J. J. Am. Chem. Soc. J. Org. Chem. J. R. J. Org. Chem. Mol. Divers, vol.1864, issue.6480, pp.6217-3405, 1056.

D. Michael, P. Mingos, D. R. Baghurst, D. Stass, J. R. Woodward et al., Microwave synthesis : chemistry at the speed of light, 51, 10403. (89) Kappe, C. O. Angew. Chemie Int. Ed96) Garbacia100) Kappe (103) Rosatelli, E. Green Chemistry and Microwave AssistedSynthesis: From Theory to Practices https, pp.15-86, 1991.

E. Da-costa-branquinho, G. Becker, C. Bouteiller, L. Jean, P. ?. Renard et al., Radiosynthesis and in vivo evaluation of fluorinated huprine derivates as PET radiotracers of acetylcholinesterase, Nuclear Medicine and Biology, vol.40, issue.4, pp.554-73, 2008.
DOI : 10.1016/j.nucmedbio.2013.02.004

URL : https://hal.archives-ouvertes.fr/hal-00996538

I. R. Baxendale, S. V. Ley, A. C. Mansfield, C. D. Smith, D. Webb et al., Multistep Synthesis Using Modular Flow Reactors: Bestmann-Ohira Reagent for the Formation of Alkynes and Triazoles, Angewandte Chemie International Edition, vol.5, issue.22, pp.4017-675, 2009.
DOI : 10.2174/1386207024607220

H. Elamari, F. Meganem, J. Herscovici, C. Girard, R. Slimi et al., Greene's Protective Groups in Organic Synthesis, Elaboration de librairies de molécules structurellement diversifiées à partir du squelette de l'acide kojique par des méthodes de synthèse micro­ondes et de flux continu, pp.658-4339, 1967.

M. Alonzi, M. P. Bracciale, A. Broggi, D. Lanari, A. Marrocchi et al., (153) Finkelstein, H. Berichte der Dtsch, Chem. Gesellschaft Monat. Chem. Bioorganic Med. Chem, vol.309, issue.18, pp.260-1528, 1910.