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Fabien Roussel Mauricette Hilly Françoise Chrétien Jean-Pierre Mauger Yves Chapleur 《Journal of carbohydrate chemistry》2013,32(6):697-707
ABSTRACT (2-Hydroxyethyl) 2-deoxy-α-D-threo-pentopyranoside 3,4,2′-trisphosphate (3) has been prepared starting from allyl-α-D-xylopyranoside. The suitably protected 2-deoxy intermediate obtained by judicious selective protection and deprotection has been phosphorylated using the phosphoramidite methodology. Final deprotection gave the expected analogue of myo-inositol 1,4,5-trisphosphate. 相似文献
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