The Construction of Novel Spirocyclic Frameworks with Cyclobutane through Rh(III)-Catalyzed [3 + 2]-Annulation between Quinoxalines and Alkynylcyclobutanols

An effective synthesis strategy for the preparation of 1'<i>H</i>-spiro[indene-1,2'-quinoxaline] has been developed. This involves a Rh(III)-catalyzed [3 + 2]-annulation of quinoxalines with alkynylcyclobutanols. The developed protocol offers a straightforward method for the preparation of versatile heterocyclic compounds with a four-membered ring and is compatible with a wide range of functional groups.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2024-09-03
DOI
https://doi.org/10.1021/acs.joc.4c00505
Citations
2
Primary Topic
Synthesis and Biological Evaluation
Type
article
Field-Weighted Citation Impact
0.50

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article

The Construction of Novel Spirocyclic Frameworks with Cyclobutane through Rh(III)-Catalyzed [3 + 2]-Annulation between Quinoxalines and Alkynylcyclobutanols

Lin Dong, Yi-Chi Gang
2 citations
The Journal of Organic Chemistry
Synthesis and Biological Evaluation
0.50
article

The Construction of Novel Spirocyclic Frameworks with Cyclobutane through Rh(III)-Catalyzed [3 + 2]-Annulation between Quinoxalines and Alkynylcyclobutanols

Lin Dong, Yi-Chi Gang
article en
2 citations

Abstract

An effective synthesis strategy for the preparation of 1'<i>H</i>-spiro[indene-1,2'-quinoxaline] has been developed. This involves a Rh(III)-catalyzed [3 + 2]-annulation of quinoxalines with alkynylcyclobutanols. The developed protocol offers a straightforward method for the preparation of versatile heterocyclic compounds with a four-membered ring and is compatible with a wide range of functional groups.

The Journal of Organic ChemistryVol. 89(18)
Sichuan University (CN)
Higher Education Discipline Innovation Project, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 40%
Synthesis and Biological Evaluation
0.50
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