1993•Bulletin of the Chemical Society of JapanRequires access

Reductive Deconjugation of α-Bromo α,β-Unsaturated Esters Based on Redox Tautomerism of Diethyl Phosphonate

Toshikazu Hirao, Keisuke Hirano, Yoshiki Ohshiro

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Abstract

Abstract Reductive deconjugation of α-bromo α,β-unsaturated esters was performed by DP(O)(OEt)2 or P(OEt)3–H2O in the presence of triethylamine from mechanistic viewpoint and was applied to the synthesis of a precursor of (±)-patulolide A.

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Abstract Reductive deconjugation of α-bromo α,β-unsaturated esters was performed by DP(O)(OEt)2 or P(OEt)3–H2O in the presence of triethylamine from mechanistic viewpoint and was applied to the synthesis of a precursor of (±)-patulolide A.

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Available abstract

Abstract Reductive deconjugation of α-bromo α,β-unsaturated esters was performed by DP(O)(OEt)2 or P(OEt)3–H2O in the presence of triethylamine from mechanistic viewpoint and was applied to the synthesis of a precursor of (±)-patulolide A.

Key concepts: Chemistry, Phosphonate, Tautomer, Redox, Medicinal chemistry, Stereochemistry, Organic chemistry, Photochemistry

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Reductive Deconjugation of α-Bromo α,β-Unsaturated Esters Based on Redox Tautomerism of Diethyl Phosphonate — Research Paper | ScholarLens