872326-49-3Relevant academic research and scientific papers
De novo asymmetric syntheses of D- and L-talose via an iterative dihydroxylation of dienoates
Ahmed, Md. Moinuddin,O'Doherty, George A.
, p. 10576 - 10578 (2005)
A short and highly efficient route to D- and L-tafo-γ-lactones has been developed. The key transformation was the sequential osmium-catalyzed bis-dihydroxylation reaction of substituted 2,4-dienoates. When the first dihydroxylation reaction is performed o
