Heteroarylation of Organophosphonium Salts with Indoles in Water: Synthesis of Symmetrical and Unsymmetrical 3,3′‐Bisindolylmethane Derivatives.

Abstract A method for the synthesis of symmetrical and unsymmetrical 3,3′‐bis(indolyl)methanes (3,3′‐BIMs) has been developed through the direct heteroarylation of indolyl‐containing di(hetero)aryl phosphonium salts with indole derivatives in aqueous media. This metal‐free reaction proceeds smoothly under mild conditions, eliminating the need for hazardous solvents and expensive additives/catalysts typically used in conventional synthesis routes, thereby highlighting the synthetic practicality and efficiency of the process. The success of this approach is largely attributed to the role of water as a promoter, facilitating the C−P bond functionalization of the phosphonium salts. Furthermore, the reaction demonstrates a broad substrate scope, good functional group tolerance, and excellent scalability. Moreover, the protocol can also be extended to the synthesis of triindolylmethane compound and diarylmethylated indole.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2024-10-16
DOI
https://doi.org/10.1002/ejoc.202400964
Citations
4
Primary Topic
Synthesis of Indole Derivatives
Type
article
Field-Weighted Citation Impact
1.00

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article

Heteroarylation of Organophosphonium Salts with Indoles in Water: Synthesis of Symmetrical and Unsymmetrical 3,3′‐Bisindolylmethane Derivatives.

Xin-Long Luo, Danhua Ge, Chao-Bin Pang, Zi-Lun Yu et al.
4 citations
European Journal of Organic Chemistry
Synthesis of Indole Derivatives
1.00
article

Heteroarylation of Organophosphonium Salts with Indoles in Water: Synthesis of Symmetrical and Unsymmetrical 3,3′‐Bisindolylmethane Derivatives.

Xin-Long Luo, Danhua Ge, Chao-Bin Pang, Zi-Lun Yu, Wen-Jun Ji, Mingming Wang
article en
4 citations

Abstract

Abstract A method for the synthesis of symmetrical and unsymmetrical 3,3′‐bis(indolyl)methanes (3,3′‐BIMs) has been developed through the direct heteroarylation of indolyl‐containing di(hetero)aryl phosphonium salts with indole derivatives in aqueous media. This metal‐free reaction proceeds smoothly under mild conditions, eliminating the need for hazardous solvents and expensive additives/catalysts typically used in conventional synthesis routes, thereby highlighting the synthetic practicality and efficiency of the process. The success of this approach is largely attributed to the role of water as a promoter, facilitating the C−P bond functionalization of the phosphonium salts. Furthermore, the reaction demonstrates a broad substrate scope, good functional group tolerance, and excellent scalability. Moreover, the protocol can also be extended to the synthesis of triindolylmethane compound and diarylmethylated indole.

European Journal of Organic ChemistryVol. 27(48)
Nanjing Tech University (CN)
National Natural Science Foundation of China, Nanjing Tech University
Openalex Percentile: Top 27%
Synthesis of Indole Derivatives
1.00
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Heteroarylation of Organophosphonium Salts with Indoles in Water: Synthesis of Symmetrical and Unsymmetrical 3,3′‐Bisindolylmethane Derivatives. — Xin-Long Luo, Danhua Ge, et al. · European Journal of Organic Chemistry (2024) | TGRS Research Map | TGRS