Carbene‐Catalyzed Enantioselective Synthesis of 1‐Oxyacylated‐2,4‐Disubstituted Cyclopentenes

Herein, we report the first carbene‐catalyzed enantioselective synthesis of multi‐functionalized oxyacylated cyclopentenes through [3 + 2] cycloaddition of α‐functionalized vinyl ketones and enals. The trisubstituted cyclopentenes were obtained with excellent enantioselectivity that could be readily converted to functionalized cyclopentenols.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2026-04-17
DOI
https://doi.org/10.1002/ejoc.70445
Primary Topic
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
Type
article
Field-Weighted Citation Impact
0.00

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article

Carbene‐Catalyzed Enantioselective Synthesis of 1‐Oxyacylated‐2,4‐Disubstituted Cyclopentenes

Hemlata Mourya, Bal Krishna Mishra, Bhoopendra Tiwari, Kajal Verma
European Journal of Organic Chemistry
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
article

Carbene‐Catalyzed Enantioselective Synthesis of 1‐Oxyacylated‐2,4‐Disubstituted Cyclopentenes

Hemlata Mourya, Bal Krishna Mishra, Bhoopendra Tiwari, Kajal Verma
article en

Abstract

Herein, we report the first carbene‐catalyzed enantioselective synthesis of multi‐functionalized oxyacylated cyclopentenes through [3 + 2] cycloaddition of α‐functionalized vinyl ketones and enals. The trisubstituted cyclopentenes were obtained with excellent enantioselectivity that could be readily converted to functionalized cyclopentenols.

European Journal of Organic Chemistry
Centre of Biomedical Research (IN), Academy of Scientific and Innovative Research (IN)
Science and Engineering Research Board
Openalex Percentile: Top 12%
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
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