Additive‐Free and Diastereoselective Synthesis for <i>Trans</i>‐Disubstituted‐2,3‐Dihydro‐Benzofurans <i>via</i> [4+1] Annulation between <i>p</i>‐QMs and TFISYs

Abstract An additive‐free and diastereoselective [4+1] annulation between ortho ‐hydroxyphenyl‐substituted para ‐quinone methides and CF 3 ‐substituted imidoyl sulfoxonium ylides is developed, providing a facile and practical route to diverse trans ‐2,3‐dihydrobenzofurans with high efficiency. This protocol features mild conditions, broad substrate scope and easy to operate.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2024-10-14
DOI
https://doi.org/10.1002/ejoc.202400946
Citations
3
Primary Topic
Asymmetric Synthesis and Catalysis
Type
article
Field-Weighted Citation Impact
0.75

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article

Additive‐Free and Diastereoselective Synthesis for Trans‐Disubstituted‐2,3‐Dihydro‐Benzofurans via [4+1] Annulation between p‐QMs and TFISYs

Chuan‐Chuan Wang, Mengru Ren, Qinglong Wang, Yajing Chen et al.
3 citations
European Journal of Organic Chemistry
Asymmetric Synthesis and Catalysis
0.75
article

Additive‐Free and Diastereoselective Synthesis for Trans‐Disubstituted‐2,3‐Dihydro‐Benzofurans via [4+1] Annulation between p‐QMs and TFISYs

Chuan‐Chuan Wang, Mengru Ren, Qinglong Wang, Yajing Chen, Yi‐Hui Li
article en
3 citations

Abstract

Abstract An additive‐free and diastereoselective [4+1] annulation between ortho ‐hydroxyphenyl‐substituted para ‐quinone methides and CF 3 ‐substituted imidoyl sulfoxonium ylides is developed, providing a facile and practical route to diverse trans ‐2,3‐dihydrobenzofurans with high efficiency. This protocol features mild conditions, broad substrate scope and easy to operate.

European Journal of Organic ChemistryVol. 27(48)
Henan University (CN), Zhengzhou University (CN), Henan Agricultural University (CN)
National Natural Science Foundation of China, Shanghai University of Traditional Chinese Medicine
Openalex Percentile: Top 32%
Asymmetric Synthesis and Catalysis
0.75
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