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Highly Stereoselective Synthesis of α-d-Mannopyranosyl Phosphosugars

[Image: see text] α-Mannopyranosyl phosphosugars are obtained in 61 to 90 % yields from 4,6-O-benzylidene-protected mannosyl thioglycosides bearing ester functionality in the 3-O-position by coupling reactions with ammonium salts of phosphosugars on activation with 1-benzenesulfinyl piperidine, 2,4,...

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Autors principals: Crich, David, Picard, Sébastien
Format: Artigo
Idioma:Inglês
Publicat: 2009
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC2852025/
https://ncbi.nlm.nih.gov/pubmed/19924835
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/jo902254w
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