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Highly diastereoselective thioglycosylation of functionalized peracetylated glycosides catalyzed by MoO2Cl2
Journal article   Peer reviewed

Highly diastereoselective thioglycosylation of functionalized peracetylated glycosides catalyzed by MoO2Cl2

Shiue-Shien Weng, Yow-Dzer Lin and Chien-Tien Chen
Organic Letters, Vol.8(24), pp.5633-5636
23/11/2006

Abstract

Among 18 oxometallic species, MoO 2 Cl 2 was found to be the most reactive in catalytic thioglycosylation of O-acetylated glycosides with functionalized thiols in CH 2 Cl 2 , leading cleanly to 1,2-trans-thioglycosides with exclusive diastereocontrol. The new catalytic protocol is applicable to a monoglycoside building block and β-(1→6)-S-linked-thiodisaccharide synthesis. © 2006 American Chemical Society.

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