852611-12-2Relevant academic research and scientific papers
De novo asymmetric syntheses of C-4-substituted sugars via an iterative dihydroxylation strategy
Ahmed, Md. Moinuddin,O'Doherty, George A.
, p. 1505 - 1521 (2007/10/03)
A short and highly efficient route to various C-4 substituted sugar lactones has been developed. The key to the overall transformation is the sequential osmium-catalyzed dihydroxylation reaction of substituted 2,4-dienoates and an allylic substitution at
De novo synthesis of galacto-sugar δ-lactones via a catalytic osmium/palladium/osmium reaction sequence
Ahmed, Md. Moinuddin,O'Doherty, George A.
, p. 3015 - 3019 (2007/10/03)
A highly efficient route to various 1,5-galacto-sugar lactones from dienoates has been developed by using three catalytic reactions. These reactions include (i) an enantioselective osmium-catalyzed dihydroxylation, (ii) a regio- and diastereoselective pal
