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Towards stable di-carba analogues of guanofosfocins
來源:黃木華長聘教授個(gè)人網(wǎng)站 發(fā)布日期:2013-03-18
作者:Jan Duchek, Mu-Hua Huang, Andrea Vasella*,
關(guān)鍵字:Antifungals,Synthesis,Carbohydrates,Heterocycles
論文來源:期刊
具體來源:Tetrahedron Letters
發(fā)表時(shí)間:2011年

Guanofosfocins are strong inhibitors of chitin synthases, but also very prone to hydrolytic cleavage. Two advanced intermediates 15 and 20 for the synthesis of stable di-carba-guanofosfocins were prepared via ester 11. Acylation of the allylic C-glycoside 6 with riburonic acid chloride 10 afforded ester 11 in 79% yield. This ester was converted to 15 in four steps and in 54% yield and to 20 in eight steps and in 20%
yield.

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