Double Isocyanide Insertion with 3‐Indolylmethanols Enabled by C–O Bond Cleavage

Comprehensive Summary The efficient construction of valuable N ‐heterocycles is one of the most important tasks in organic synthesis. Pyrrolo[2,3‐ b ]indoles represent a privileged skeleton, which are extensively found in natural products, pharmaceuticals and luminescent materials. Nevertheless, their synthesis suffers from pre‐functionalized starting materials and multi‐step synthesis. On the other hand, despite significant progress in isocyanide insertions, it remains underdeveloped for multiple isocyanide insertion initiated from inert C–O bond activation. Herein, we report an unprecedented TMSOTf‐catalyzed domino reaction enabled by C–O bond activation, where double isocyanide insertion with 3‐indolylmethanols and sequential intramolecular cyclization are involved to afford cyano‐substituted pyrrolo[2,3‐ b ]indoles. Isocyanides, which have generally been utilized as the sole C1 building block, are employed as both C ‐nucleophiles and masked N ‐nucleophiles to produce the cyano‐substituted pyrrole skeleton. The crucial chloranil oxidant assists the electronic property variation of the indole motif, facilitating the nucleophilic attack at both benzylic and C2 positions of 3‐indolylmethanols. This newly established protocol features mild conditions, good functional group tolerance and broad substrate scope. Depending on the substituent of the isocyanide, corresponding amide and cyclopenta[ b ]indole scaffold could also be accessed. Moreover, diverse transformations of the obtained product are illustrated, including deprotection and hydrolysis. The successful formation of various types of N ‐containing polycyclic compounds further demonstrates the remarkable synthetic potential inherent of the given protocol. After careful mechanistic studies, the enamine compound, generated from double isocyanide insertion with 3‐indolylmethanols, is proposed as the key intermediate for this reaction.

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Publication Details

Journal
Chinese Journal of Chemistry
Published
2025-10-27
DOI
https://doi.org/10.1002/cjoc.70342
Citations
1
Primary Topic
Synthesis of Indole Derivatives
Type
article
Field-Weighted Citation Impact
0.94

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article

Double Isocyanide Insertion with 3‐Indolylmethanols Enabled by C–O Bond Cleavage

Chang‐Hua Ding, Xiaomei Huang, Bin Xu, Zhenkun Yang et al.
1 citations
Chinese Journal of Chemistry
Synthesis of Indole Derivatives
0.94
article

Double Isocyanide Insertion with 3‐Indolylmethanols Enabled by C–O Bond Cleavage

Chang‐Hua Ding, Xiaomei Huang, Bin Xu, Zhenkun Yang, Mingchun Gao, Zhicheng Chen
article en
1 citations

Abstract

Comprehensive Summary The efficient construction of valuable N ‐heterocycles is one of the most important tasks in organic synthesis. Pyrrolo[2,3‐ b ]indoles represent a privileged skeleton, which are extensively found in natural products, pharmaceuticals and luminescent materials. Nevertheless, their synthesis suffers from pre‐functionalized starting materials and multi‐step synthesis. On the other hand, despite significant progress in isocyanide insertions, it remains underdeveloped for multiple isocyanide insertion initiated from inert C–O bond activation. Herein, we report an unprecedented TMSOTf‐catalyzed domino reaction enabled by C–O bond activation, where double isocyanide insertion with 3‐indolylmethanols and sequential intramolecular cyclization are involved to afford cyano‐substituted pyrrolo[2,3‐ b ]indoles. Isocyanides, which have generally been utilized as the sole C1 building block, are employed as both C ‐nucleophiles and masked N ‐nucleophiles to produce the cyano‐substituted pyrrole skeleton. The crucial chloranil oxidant assists the electronic property variation of the indole motif, facilitating the nucleophilic attack at both benzylic and C2 positions of 3‐indolylmethanols. This newly established protocol features mild conditions, good functional group tolerance and broad substrate scope. Depending on the substituent of the isocyanide, corresponding amide and cyclopenta[ b ]indole scaffold could also be accessed. Moreover, diverse transformations of the obtained product are illustrated, including deprotection and hydrolysis. The successful formation of various types of N ‐containing polycyclic compounds further demonstrates the remarkable synthetic potential inherent of the given protocol. After careful mechanistic studies, the enamine compound, generated from double isocyanide insertion with 3‐indolylmethanols, is proposed as the key intermediate for this reaction.

Chinese Journal of ChemistryVol. 44(2)
Shanghai University (CN), Shanghai University of Engineering Science (CN), Chinese Academy of Sciences (CN), Guangdong Academy of Agricultural Sciences (CN), Shanghai Institute of Organic Chemistry (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 20%
Synthesis of Indole Derivatives
0.94
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