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Protecting Group Manipulations on Glycosyl Phosphate Triesters
Authors:Frédéric R. Carrel
Affiliation:Laboratory of Organic Chemistry , Swiss Federal Institute of Technology (ETH) , Wolfgang‐Pauli‐Strasse 10, Zürich, Switzerland
Abstract:

Glucosyl and mannosyl phosphate triester building blocks were differentially protected by protecting group manipulations on competent glycosyl donors. Dibutyl 3,4‐di‐O‐benzyl‐6‐O‐(fluorenylmethoxycarbonyl)‐2‐O‐pivaloyl‐β‐D‐glucopyranoside phosphate, not accessible by other methods, was prepared this way.
Keywords:Glycosyl phosphate triester  Protecting group manipulation
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