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March 3, 2026Organic Letters6 citations

Catalytic Asymmetric Synthesis of 1,2-Fused Tricyclic Indoles Containing an Eight-Membered Biaryl Bridge

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HFHao FengSun Yat-sen UniversityHHHeyu HuJiangxi University of Traditional Chinese MedicineJZJunling ZhaoSun Yat-sen University

Key Points

  • Products exhibit both central and axial chirality, indicating a complex structure.
  • High yields and stereoselectivities were achieved through the Friedel-Crafts alkylation process.
  • Catalyzed by In(OTf)3-pybox complex, showcasing an effective method for synthesis.
  • The study demonstrates potential for scale-up reactions and product derivatization.

Abstract

We disclose herein a diastereo- and enantioselective synthesis of tricyclic indoles containing an eight-membered-ring-bridged biaryl architecture from 2-(2-aminoaryl)indoles and β,γ-unsaturated α-ketoesters. This Friedel-Crafts alkylation/dehydration process was efficiently catalyzed by an In(OTf)3-pybox complex to give the products featuring both central and axial chirality in generally high yields and stereoselectivities. A scale-up reaction and derivatization of the representative products were performed to study the synthetic potential of this transformation.

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Cite This Study

Feng et al. (2026) studied this question.

synapsesocial.com/papers/69a75c20c6e9836116a249fehttps://doi.org/10.1021/acs.orglett.5c05359
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