4.8 Article

Construction of Vicinal Tertiary and All-Carbon Quaternary Stereocenters via Ir-Catalyzed Regio-, Diastereo-, and Enantioselective Allylic Alkylation and Applications in Sequential Pd Catalysis

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JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 135, 期 29, 页码 10626-10629

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AMER CHEMICAL SOC
DOI: 10.1021/ja4052075

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资金

  1. NIH-NIGMS [R01GM080269]
  2. Amgen
  3. Gordon and Betty Moore Foundation
  4. Caltech
  5. Shanghai Institute of Organic Chemistry (SIOC)

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Highly congested vicinal stereocenters comprised of tertiary and all-carbon quaternary centers were generated via Ir-catalyzed asymmetric allylic alkylation of beta-ketoesters. These catalytic reactions proceed in excellent yields with a broad scope on either reaction partner and with outstanding regio-, diastereo-, and enantiocontrol. Implementation of a subsequent Pd-catalyzed alkylation affords dialkylated products with pinpoint stereochemical control of both chiral centers.

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