Ag(I)‐Catalyzed Intramolecular Cascade Cyclization to Construct [6–5–7–6] Heterotetracyclic (−N and −O) Indole Fused Scaffolds

Abstract Herein, we report a silver‐catalyzed intramolecular cascade reaction of 2‐alkynylaniline tethered heteroenone systems to achieve the synthesis of [6–5–7–6] heterotetracyclic indole fused benzoxepino‐ and benzoazepino scaffolds. The reaction proceeded through a silver(I)‐initiation cascade intramolecular 5‐endo‐dig cyclization followed by 7‐exo‐trig cyclization to enable the structurally diverse [6–5–7–6] heterotetracyclic adducts in modest to good yields.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2025-03-24
DOI
https://doi.org/10.1002/adsc.202500140
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.00

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article

Ag(I)‐Catalyzed Intramolecular Cascade Cyclization to Construct [6–5–7–6] Heterotetracyclic (−N and −O) Indole Fused Scaffolds

Avijit Goswami, Madan Kumar, Ankush Kumar, Soni Devi
Advanced Synthesis & Catalysis
Catalytic C–H Functionalization Methods
article

Ag(I)‐Catalyzed Intramolecular Cascade Cyclization to Construct [6–5–7–6] Heterotetracyclic (−N and −O) Indole Fused Scaffolds

Avijit Goswami, Madan Kumar, Ankush Kumar, Soni Devi
article en

Abstract

Abstract Herein, we report a silver‐catalyzed intramolecular cascade reaction of 2‐alkynylaniline tethered heteroenone systems to achieve the synthesis of [6–5–7–6] heterotetracyclic indole fused benzoxepino‐ and benzoazepino scaffolds. The reaction proceeded through a silver(I)‐initiation cascade intramolecular 5‐endo‐dig cyclization followed by 7‐exo‐trig cyclization to enable the structurally diverse [6–5–7–6] heterotetracyclic adducts in modest to good yields.

Advanced Synthesis & CatalysisVol. 367(12)
Indian Institute of Technology Ropar (IN)
Science and Engineering Research Board
Openalex Percentile: Top 96%
Catalytic C–H Functionalization Methods
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