Carbohydrate research

Deoxygenation at the C3 position of d-and l-arabinofuranose: stereospecific access to enantiomeric cordycepose derivatives

F da Paixão Soares, MJ e Silva, B Doboszewski

Index: Da Paixao Soares, Fabio; Silva, Maria Joselice E; Doboszewski, Bogdan Carbohydrate Research, 2013 , vol. 380, p. 143 - 148

Full Text: HTML

Citation Number: 1

Abstract

Abstract Efficient synthesis of 3-deoxy-1, 2-O-isopropylidene-β-d-and β-l-threo- pentofuranose (1, 2-O-isopropylidene-β-d-and β-l-cordycepose) was accomplished starting from d-and l-arabinofuranose derivatives, respectively, by the action of LiBH (Et) 3 on corresponding intermediate 3-O-lyxofuranosyl trifluoromethanesulfonates.

Related Articles:

An efficient synthesis of sulfonylhydrazides and sulfonylsemicarbazides by utilizing alumina as a catalyst

[Safaei-Ghomi, Javad Journal of the Chinese Chemical Society, 2007 , vol. 54, # 6 p. 1561 - 1563]

Controlled release of volatile aldehydes and ketones from dynamic mixtures generated by reversible hydrazone formation

[Helvetica Chimica Acta, , vol. 90, # 12 p. 2281 - 2314]

Importance of repulsion of lone electron pairs in the enhanced reactivity of 1, 8-naphthyridine and the large α-effect of hydrazine in the aminolyses of p-toluenesulfonyl …

[Canadian Journal of Chemistry, , vol. 64, p. 1184 - 1188]

More Articles...