Stereoselective synthesis of C-glycosides from carboxylic acids: the tandem Tebbe–Claisen approach†
Abstract
A variety of β- or α-C-glycosides may be readily accessed in an entirely stereoselective fashion from
* Corresponding authors
a Dyson Perrins Laboratory, Oxford University, South Parks Road, Oxford, UK
b Celltech R & D, Granta Park, Great Abington, Cambridge, UK
A variety of β- or α-C-glycosides may be readily accessed in an entirely stereoselective fashion from
H. Y. Godage, D. J. Chambers, G. R. Evans and A. J. Fairbanks, Org. Biomol. Chem., 2003, 1, 3772 DOI: 10.1039/B306675B
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