TY - JOUR
T1 - Pd(II)-Catalyzed Asymmetric [4 + 1] Annulation via Ligand Relay-Enabled Carbenylative Insertion/E1cB-Type Heck Cascade
AU - Luo, Zhou
AU - Zhang, Yi Hao
AU - Zhang, Chao
AU - Dong, Kewei
AU - Pramanick, Pranab K.
AU - Zhao, Shen
AU - Liu, Yuanyuan
AU - Yang, Guoqiang
N1 - Publisher Copyright:
© 2026 American Chemical Society
PY - 2026/2/4
Y1 - 2026/2/4
N2 - 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.
AB - 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.
UR - https://www.scopus.com/pages/publications/105029188647
U2 - 10.1021/jacs.5c20265
DO - 10.1021/jacs.5c20265
M3 - 文章
C2 - 41571622
AN - SCOPUS:105029188647
SN - 0002-7863
VL - 148
SP - 4605
EP - 4614
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 4
ER -