P <sub>4</sub> S <sub>10</sub> ‐Promoted [5+1] Spiroannulation of 2‐(2‐Nitrophenyl)‐indoles with Cyclic Ketones to Access Spirocyclic Tetrahydrocarbolines

A P 4 S 10 ‐promoted [5 + 1] spiroannulation of 2‐(2‐nitrophenyl)‐indoles with cyclic ketones for the preparation of spirocyclic tetrahydrocarbolines has been described. The present approach afforded a series of structurally valuable spirocyclic tetrahydrocarbolines in moderate to good yields under metal‐free conditions. In this work, nitro reduction, C–N condensation, and spiroannulation were realized in one pot.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2025-11-24
DOI
https://doi.org/10.1002/adsc.70244
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
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article

P 4 S 10 ‐Promoted [5+1] Spiroannulation of 2‐(2‐Nitrophenyl)‐indoles with Cyclic Ketones to Access Spirocyclic Tetrahydrocarbolines

Xueao Wang, Bin Tan, Shanping Chen, Guo‐Jun Deng et al.
Advanced Synthesis & Catalysis
Catalytic C–H Functionalization Methods
article

P 4 S 10 ‐Promoted [5+1] Spiroannulation of 2‐(2‐Nitrophenyl)‐indoles with Cyclic Ketones to Access Spirocyclic Tetrahydrocarbolines

Xueao Wang, Bin Tan, Shanping Chen, Guo‐Jun Deng, Jiao Liu, Yidong Liu, Qi Yin
article en

Abstract

A P 4 S 10 ‐promoted [5 + 1] spiroannulation of 2‐(2‐nitrophenyl)‐indoles with cyclic ketones for the preparation of spirocyclic tetrahydrocarbolines has been described. The present approach afforded a series of structurally valuable spirocyclic tetrahydrocarbolines in moderate to good yields under metal‐free conditions. In this work, nitro reduction, C–N condensation, and spiroannulation were realized in one pot.

Advanced Synthesis & CatalysisVol. 368(2)
Xiangtan University (CN), Henan Normal University (CN)
Openalex Percentile: Top 73%
Catalytic C–H Functionalization Methods
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