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Org Lett ; 13(4): 576-9, 2011 Feb 18.
Article in English | MEDLINE | ID: mdl-21244043

ABSTRACT

The use of manganese(III) acetate allows the direct synthesis of diverse arrays of [4.3.0] bicyclic carbohydrate-based γ-lactone building blocks from glycals. A mechanism to explain the high regio- and stereoselectivity is proposed. The new reaction has the potential to generate libraries for biological screening.


Subject(s)
4-Butyrolactone/analogs & derivatives , 4-Butyrolactone/chemical synthesis , Carbohydrates/chemical synthesis , 4-Butyrolactone/chemistry , Acetates/chemistry , Carbohydrates/chemistry , Combinatorial Chemistry Techniques , Magnesium/chemistry , Molecular Structure , Stereoisomerism
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