A Highly Diastereoselective Synthesis of α-Substituted-β-hydroxy Compounds from Corresponding β-Stannyl Compounds
Access this Article
Search this Article
Anti-β-stannyl-α-substituted carbonyl compounds were completely converted to its syn-analogues, and each diastereomer was oxidized to its β-hydroxylated analogues with retention of the stereochemistry.
- Chemistry Letters
Chemistry Letters 1997(10), 1035-1036, 1997-10
The Chemical Society of Japan