Diastereoselectivity in the directed ald
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Charles W. Jefford; Danielle Jaggi; John Boukouvalas
📂
Article
📅
1987
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Elsevier Science
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French
⚖ 247 KB
Threo and erythro-6-hydroxy-a,fi-unsaturated -y-lactones are obtained with useful diastereoselection by condensing 2-trimethylsiloxyfuran and aldehydes by varying the reaction reaction conditions. A stereomechanistic rationale is presented together with a practical two-step synthesis of the threo a