Highly Diastereoselective Synthesis of 2,3-Dihydropyrroles via Formal [4 + 1] Annulation Reaction of α,β-Unsaturated Imines and <i>in Situ</i> Generated Pyridinium Ylide

We report a cascade approach for the synthesis of 2,3-dihydropyrroles derivatives via a formal [4 + 1] annulation reaction of α,β-unsaturated imines with <i>in situ</i> generated pyridinium ylides. Importantly, this protocol is compatible with diverse substituted imines as well as pyridinium ylides, constructing 2,3-dihydropyrroles with excellent yield and selectivity. Thereafter, the Merrifield resin-supported pyridinium ylide as a potential C1 synthon was also employed in our strategy and reused several times, resulting in products with excellent yield and diastereoselectivity.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2024-12-20
DOI
https://doi.org/10.1021/acs.joc.4c02320
Citations
2
Primary Topic
Cyclopropane Reaction Mechanisms
Type
article
Field-Weighted Citation Impact
0.50

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article

Highly Diastereoselective Synthesis of 2,3-Dihydropyrroles via Formal [4 + 1] Annulation Reaction of α,β-Unsaturated Imines and in Situ Generated Pyridinium Ylide

Anupriya Bera, Akanksha Kumari, Khyati Shukla, Nirmal K. Rana et al.
2 citations
The Journal of Organic Chemistry
Cyclopropane Reaction Mechanisms
0.50
article

Highly Diastereoselective Synthesis of 2,3-Dihydropyrroles via Formal [4 + 1] Annulation Reaction of α,β-Unsaturated Imines and in Situ Generated Pyridinium Ylide

Anupriya Bera, Akanksha Kumari, Khyati Shukla, Nirmal K. Rana, Suman Saha
article en
2 citations

Abstract

We report a cascade approach for the synthesis of 2,3-dihydropyrroles derivatives via a formal [4 + 1] annulation reaction of α,β-unsaturated imines with <i>in situ</i> generated pyridinium ylides. Importantly, this protocol is compatible with diverse substituted imines as well as pyridinium ylides, constructing 2,3-dihydropyrroles with excellent yield and selectivity. Thereafter, the Merrifield resin-supported pyridinium ylide as a potential C1 synthon was also employed in our strategy and reused several times, resulting in products with excellent yield and diastereoselectivity.

The Journal of Organic ChemistryVol. 90(1)
Indian Institute of Technology Jodhpur (IN)
Ministry of Education, India, Science and Engineering Research Board
Openalex Percentile: Top 37%
Cyclopropane Reaction Mechanisms
0.50
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Highly Diastereoselective Synthesis of 2,3-Dihydropyrroles via Formal [4 + 1] Annulation Reaction of α,β-Unsaturated Imines and <i>in Situ</i> Generated Pyridinium Ylide — Anupriya Bera, Akanksha Kumari, et al. · The Journal of Organic Chemistry (2024) | TGRS Research Map | TGRS