Carbohydrate Chemistry by Rauter, Amelia Pilar; Lindhorst, Thisbe; Queneau, Yves

By Rauter, Amelia Pilar; Lindhorst, Thisbe; Queneau, Yves

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A major contribution of Lubineau in water-promoted organic reactions was the pioneering work concerning the acceleration of aldolisation 12 | Carbohydr. , 2014, 40, 11–30 View Online Ph O O O O O OA ll O OBn 16 h MO 2C re face facial selectivity: 97/3 MO2C sugar 60 °C 99 % M = (-)-menthyl 12/04/2014 11:51:13. 1039/9781849739986-00011 Scheme 1 O OSiMe3 O OH Ph OH Ph + + PhCHO anti syn Scheme 2 O + + COMe COMe endo exo activation parameters (kJ . 9 Stereoselectivity was reversed in water affording syn adducts as the major isomers.

M. Trost, Science, 1991, 254, 1471. R. A. Sheldon, Chem. , London, 1992, 903. 11: PBT Assessment – May 2008. echa. pdf? vers= 20_08_08. (a) D. Specker and V. Wittmann, Top. Curr. , 2007, 267, 65; and (b) P. Compain and O. R. Martin, Bioorg. Med. , 2001, 9, 3077. F. Rodrigues, Y. Canac and A. Lubineau, Chem. , 2000, 2049. D. E. Levy, The Organic Chemistry of Sugars, CRC Press LLC, 2006, 269. ´me ´ria, (a) Y. Hersant, R. Abou-Jneid, Y. Canac, A. Lubineau, M. Philippe, D. Se X. Radisson and M-C. Scherrmann, Carbohydr.

Auge ´, Top. Curr. , 1999, 206, 1. Lubineau and J. Auge (a) F. Garcia Calvo-Flores, ChemSusChem, 2009, 2, 905; and (b) P. Anastas and N. Eghbali, Chem. Soc. , 2010, 39, 301. , 2008, 10, 225; and (b) J. -C. (a) J. Auge Scherrmann, New J. , 2012, 36, 1091. 26 | Carbohydr. , 2014, 40, 11–30 View Online 5 6 7 12/04/2014 11:51:13. 1039/9781849739986-00011 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 `le, New J. , 1980, 4, 547. S. David, A. Lubineau and J-M.

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