Article ID Journal Published Year Pages File Type
1348335 Tetrahedron: Asymmetry 2007 4 Pages PDF
Abstract
A stereoselective synthesis of (6S)-5,6-dihydro-6-[(2R)-2-hydroxy-6-phenylhexyl]-2H-pyran-2-one is reported. The strategy utilizes an olefin cross-metathesis, syn-benzylidene acetal formation and a preferential (Z)-Wittig olefination reaction and lactonization as the key steps.
Related Topics
Physical Sciences and Engineering Chemistry Inorganic Chemistry
Preview
Stereoselective synthesis of (6S)-5,6-dihydro-6-[(2R)-2-hydroxy-6-phenylhexyl]-2H-pyran-2-one
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