Catalytic Enantioselective Cyclopropanation of α‑Fluoroacrylates: An Experimental and Theoretical Study

Herein, we report the catalytic asymmetric synthesis of functionalized fluorocyclopropanes from α-fluoroacrylates. The method using Rh2((S)-TCPTTL)4 allowed the difficult reaction of an in situ-generated electrophilic Rh-carbene with an electron-poor α-fluoroacrylate. The desired fluorocyclopropanes...

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Veröffentlicht in:ACS catalysis 2019-03, Vol.9 (3), p.2594-2598
Hauptverfasser: Pons, Amandine, Tognetti, Vincent, Joubert, Laurent, Poisson, Thomas, Pannecoucke, Xavier, Charette, André B, Jubault, Philippe
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Sprache:eng
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Zusammenfassung:Herein, we report the catalytic asymmetric synthesis of functionalized fluorocyclopropanes from α-fluoroacrylates. The method using Rh2((S)-TCPTTL)4 allowed the difficult reaction of an in situ-generated electrophilic Rh-carbene with an electron-poor α-fluoroacrylate. The desired fluorocyclopropanes were obtained in good yields, excellent dr and ee. Finally, the mechanism of this transformation was studied by density functional theory (DFT) calculations to explain the particular reactivity of the donor–acceptor diazo compounds with electron-deficient α-fluoroacrylates.
ISSN:2155-5435
2155-5435
DOI:10.1021/acscatal.9b00354