Accessing [6,6,5,6] tetracyclic indeno-quinolines via photomediated cascade reaction of electron-rich 1,7-enynes

P. Ashok Yadav; Anand Varma; Purushothaman Gopinath

doi:10.1039/d5cc04023j

January 1, 2025Chemical CommunicationsOpen Access

Accessing [6,6,5,6] tetracyclic indeno-quinolines via photomediated cascade reaction of electron-rich 1,7-enynes

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Key Points

The reaction produces various sulfonyl and trifluoromethyl decorated tetracyclic indeno-quinolines.
It demonstrates a broad substrate scope, indicating versatility in chemical synthesis.
The method involves a cascade radical addition-cyclization-aromatization sequence, enhancing synthetic efficiency.
Good functional group tolerance is evident, suggesting wide applicability for complex molecular structures.

Implication

Synthesis reveals broad substrate scope and good functional group tolerance in indeno-quinolines.

Abstract

Synthesisof various sulfonyl and trifluoromethyl decorated tetracyclic indeno-quinolines from 1,7-enynes via a cascade radical addition-cyclization-aromatization sequence is presented. The reaction shows broad substrate scope with good functional group tolerance on...

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Cite This Study

Yadav et al. (2025) studied this question.

synapsesocial.com/papers/68c198cd9b7b07f3a061ade9 https://doi.org/10.1039/d5cc04023j

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Accessing [6,6,5,6] tetracyclic indeno-quinolines via photomediated cascade reaction of electron-rich 1,7-enynes

Key Points

Implication

Abstract

Discussion

Cite This Study

Accessing [6,6,5,6] tetracyclic indeno-quinolines via photomediated cascade reaction of electron-rich 1,7-enynes

Key Points

Implication

Abstract

Discussion

Cite This Study

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