4.7 Review

Enantioselective palladium-catalyzed allylic alkylation reactions in the synthesis of Aspidosperma and structurally related monoterpene indole alkaloids

期刊

NATURAL PRODUCT REPORTS
卷 35, 期 6, 页码 559-574

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7np00069c

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资金

  1. NIH-NIGMS [R01GM080269]
  2. Amgen
  3. Gordon and Betty Moore Foundation
  4. Caltech
  5. NSF [DGE-1144469]
  6. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM080269] Funding Source: NIH RePORTER

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Enantioselective Pd-catalyzed allylic alkylations of prochiral enolates represent a powerful tool for the construction of all-carbon quaternary stereocenters. This review describes the emergence of such reactions as strategic linchpins that enable efficient, stereocontrolled syntheses of Aspidosperma and related monoterpene indole alkaloids.

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