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.
Authors
- Anupriya Bera
- Akanksha Kumari (ORCID: https://orcid.org/0000-0003-2531-2329)
- Khyati Shukla (ORCID: https://orcid.org/0000-0001-5106-925X)
- Nirmal K. Rana (ORCID: https://orcid.org/0000-0001-9224-2725)
- Suman Saha (ORCID: https://orcid.org/0000-0001-8829-1815)
Institutions
- Indian Institute of Technology Jodhpur (IN)
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
Funders
- Ministry of Education, India
- Science and Engineering Research Board