ChemInform Abstract: Enantioselective Cascade Formal Reductive Insertion of Allylic Alcohols into the C(O)-C Bond of 1,3-Diketones: Ready Access to Synthetically Valuable 3-Alkylpentanol Units

Functionalized γ‐chiral alcohols are prepared via an unprecedented cascade reaction which combines dual iron—amine‐catalyzed enantioselective functionalization of allylic alcohols and chemoselective acyl transfer.

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Veröffentlicht in:ChemInform 2014-12, Vol.45 (48), p.no-no
Hauptverfasser: Roudier, Mylene, Constantieux, Thierry, Quintard, Adrien, Rodriguez, Jean
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container_title ChemInform
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creator Roudier, Mylene
Constantieux, Thierry
Quintard, Adrien
Rodriguez, Jean
description Functionalized γ‐chiral alcohols are prepared via an unprecedented cascade reaction which combines dual iron—amine‐catalyzed enantioselective functionalization of allylic alcohols and chemoselective acyl transfer.
doi_str_mv 10.1002/chin.201448022
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source Wiley Online Library Journals Frontfile Complete
subjects C-C bond formation
catalysis
catalysis, phase‐transfer catalysis
diastereoselective syntheses
diastereoselective syntheses, enantioselective syntheses (incl. cis/trans‐isomerism)
enantioselective syntheses (incl. cis/trans-isomerism)
insertion reactions
phase-transfer catalysis
title ChemInform Abstract: Enantioselective Cascade Formal Reductive Insertion of Allylic Alcohols into the C(O)-C Bond of 1,3-Diketones: Ready Access to Synthetically Valuable 3-Alkylpentanol Units
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