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Pd(II)-Catalyzed Asymmetric [4 + 1] Annulation via Ligand Relay-Enabled Carbenylative Insertion/E1cB-Type Heck Cascade

  • Zhou Luo
  • , Yi Hao Zhang
  • , Chao Zhang
  • , Kewei Dong
  • , Pranab K. Pramanick
  • , Shen Zhao
  • , Yuanyuan Liu*
  • , Guoqiang Yang*
  • *Corresponding author for this work
  • East China Normal University
  • Shanghai Jiao Tong University

Research output: Contribution to journalArticlepeer-review

Abstract

Pd-catalyzed asymmetric annulation via metal carbene is highly desired for efficient access to chiral cyclic compounds; however, such a strategy remains a considerable challenge. In this study, we report an unprecedented Pd-catalyzed asymmetric [4 + 1] annulation through a tandem carbene migratory insertion/Heck reaction, facilitated by an asymmetric ligand relay strategy. This approach provides an efficient protocol to access enantio-enriched α-alkylidene 3-substituted indanones. A wide range of substrates could be tolerated in the catalytic system, furnishing products with good to excellent enantioselectivity. A mechanistic study has also been conducted, which offers insights into the ligand relay catalytic system. Control experiments and DFT calculations elucidated a plausible novel E1cB mechanism for the elimination step of the Heck process, well explaining the generation of the olefin product of the Heck reaction bearing an unusual configuration. The enantio-determining step is revealed by DFT calculations to be a concerted process involving carbene formation and migratory insertion.

Original languageEnglish
Pages (from-to)4605-4614
Number of pages10
JournalJournal of the American Chemical Society
Volume148
Issue number4
DOIs
StatePublished - 4 Feb 2026

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