Rhodium‐Catalyzed Synthesis of Polycyclic Spiroindolines via Intramolecular 1,2‐Acyloxy Migration‐Cyclization Cascade

Abstract Herein, a novel and efficient protocol for the synthesis of polycyclic spiroindolines is realized through a 1,2‐acyloxy migration‐cyclization cascade starting from ester‐tethered 1,2,3‐triazoles. [6,5,5,6] and [6,5,6,6] ring skeleton are constructed in moderate to excellent yields.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2024-09-06
DOI
https://doi.org/10.1002/ejoc.202400944
Citations
4
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
1.00
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article

Rhodium‐Catalyzed Synthesis of Polycyclic Spiroindolines via Intramolecular 1,2‐Acyloxy Migration‐Cyclization Cascade

Ze‐Feng Xu, Chuan‐Ying Li, Jing Chen, Mingming Yu et al.
4 citations
European Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
1.00
article

Rhodium‐Catalyzed Synthesis of Polycyclic Spiroindolines via Intramolecular 1,2‐Acyloxy Migration‐Cyclization Cascade

Ze‐Feng Xu, Chuan‐Ying Li, Jing Chen, Mingming Yu, Zhuoya Chen
article en
4 citations

Abstract

Abstract Herein, a novel and efficient protocol for the synthesis of polycyclic spiroindolines is realized through a 1,2‐acyloxy migration‐cyclization cascade starting from ester‐tethered 1,2,3‐triazoles. [6,5,5,6] and [6,5,6,6] ring skeleton are constructed in moderate to excellent yields.

European Journal of Organic ChemistryVol. 27(48)
Zhejiang Sci-Tech University (CN)
Openalex Percentile: Top 27%
Catalytic C–H Functionalization Methods
1.00
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