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29 D. J. Dixon, S. V. Ley and E. W. Tate, J. Chem. Soc., Perkin Trans. 1, 1998, 3125.
30 P. Lucio Anelli, C. Bi, F. Montanari and S. Quici, J. Org. Chem., 1987, 52,
2559; R. Siedlecka, J. Skarzewski and J. Mlochowski, Tetrahedron Lett., 1990,
31, 2177.
31 E. Marcantoni, F. Nobili, G. Bartoli, M. Bosco and L. Sambri, J. Org. Chem.,
1997, 62, 4183.
32 K. J. Eash, M. S. Pulia, L. C. Wieland and R. S. Mohan, J. Org. Chem., 2000, 65,
8399.
33 G. Balme and J. Gore, J. Org. Chem., 1983, 48, 3336.
34 A. Mathieu, PhD thesis, University of Paris Sud, France, 2009.
35 F. Garro-Helion, A. Merzouk and F. Guibe, J. Org. Chem., 1993, 58, 6109.
36 M. Chandler, M. J. Bamford, R. Conroy, B. Lamont, B. Patel, V. K. Patel, I. P.
Steeples, R. Storer, N. G. Weir, M. Wright and C. Williamson, J. Chem. Soc.-
Perkin Trans. 1, 1995, 1173.
37 G. V. Reddy, G. V. Rao and D. S. Iyengar, Tetrahedron Lett., 1999, 40, 3937.
38 For some key reviews see: (a) L. F. Tietze, Chem. Rev., 1996, 96, 115; (b) S. E.
Denmark and A. Thorarensen, Chem. Rev., 1996, 96, 137; (c) D. E. Fogg and
E. N. dos Santos, Coord. Chem. Rev., 2004, 248, 2365; (d) A. Ajamian and J. L.
Gleason, Angew. Chem., Int. Ed., 2004, 43, 3754; (e) J.-C. Wasilke, S. J. Obrey,
R. T. Baker and G. C. Bazan, Chem. Rev., 2005, 105, 1001; (f) D. Enders, C.
Grondal and M. R. M. H¨ttl, Angew. Chem. Int. Ed., 2007, 46, 1570; and (g) N.
Shindoh, Y. Takemoto and K. Takasu, Chem. Eur. J., 2009, 15, 12168.
39 A. Français, D. Urban and J.-M. Beau, Angew. Chem. Int. Ed., 2007, 46,
8662.
40 A similar work using TMSOTf as catalyst was also reported: C.-C. Wang, J.-C.
Lee, S.-Y. Luo, S. S. Kulkarni, Y.-W. Huang, C.-C. Lee, K.-L. Chang and S.-C.
Hung, Nature, 2007, 446, 896.
41 Y. Bourdreux, A. Lem
´
tais, D. Urban and J.-M. Beau, Chem. Commun., 2011,
47, 2146.
42 J. Guiard, A. Collmann, M. Gilleron, L. Mori, G. De Libero, J. Prandi and G.
Puzo, Angew. Chem. Int. Ed., 2008, 47, 9734.
43 M. Gilleron, S. Stenger, Z Mazorra, F. Wittke, S. Mariotti, G. B
¨
hmer, J.
Prandi, L. Mori, G. Puzo and G. De Libero, J. Exp. Med., 2004, 199, 649.
44 A. Lem´tais, Y. Bourdreux, P. Lesot, J. Farjon and J.-M. Beau, J. Org. Chem.,
2013, 78, 7648.
45 B. Gau, A. Lem´tais, M. Lepore, L. F. Garcia-Alles, Y. Bourdreux, L. Mori,
M. Gilleron, G. De Libero, G. Puzo, J.-M. Beau and J. Prandi, ChemBioChem,
2013, 14, 2413.
46 For the selective removal of benzyl groups in the presence of benzylidene
acetals using ammonium formate as a hydrogen donor, see for example:
(a) T. Bieg and W. Szeja, Synthesis, 1985, 76; (b) D. Beaupere, I. Boutbaiba,
G. Demailly and R. Uzan, Carbohydr. Res., 1988, 180, 152.
47 For another synthesis of a di-O-acylated sulfoglycolipid see: D. Geerdink, B.
ter Horst, M. Lepore, L. Mori, G. Puzo, A. K. H. Hirsch, M. Gilleron, G. De
Libero and A. J. Minnaard, Chem. Sci., 2013, 4, 709.
48 M. Sakagami and H. Hamana, Tetrahedron Lett., 2000, 41, 5547.
49 X. M. Zhu and R. R. Schmidt, Angew. Chem. Int. Ed., 2009, 48, 1900.
50 B. Ernst, G. W. Hart, P. Sina¨, ed., Carbohydrates in Chemistry and Biology,
Wiley-VCH, 2000, Vol. 1, p. 1064.
51 D. B. Werz, R. Ranzinger, S. Herget, A. Adibekian, C.-W. Lieth and P. H.
Seeberger, ACS Chem. Biol., 2007, 2, 685.
52 A. V. Demchenko, ed., Handbook of Chemical Glycosylation, Wiley-VCH, 2008,
p. 501.
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