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

IF 3.6 2区 化学 Q1 CHEMISTRY, ORGANIC Journal of Organic Chemistry Pub Date : 2024-12-20 DOI:10.1021/acs.joc.4c02320
Suman K. Saha, Anupriya Bera, Akanksha Kumari, Khyati Shukla, Nirmal K. Rana
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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 in situ 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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α,β-不饱和亚胺与原位生成吡啶的正[4 + 1]环化反应合成2,3-二氢吡咯的高度非对映选择性
我们报道了一种通过α,β-不饱和亚胺与原位生成的吡啶类化合物的形式[4 + 1]环反应合成2,3-二氢吡咯衍生物的级联方法。重要的是,该方法与多种取代亚胺以及吡啶类化合物兼容,构建了具有优异收率和选择性的2,3-二氢吡咯。此后,我们的策略中也采用了Merrifield树脂负载的吡啶ylide作为潜在的C1合成物,并多次重复使用,得到了收率和非对映选择性都很好的产品。
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来源期刊
Journal of Organic Chemistry
Journal of Organic Chemistry 化学-有机化学
CiteScore
6.20
自引率
11.10%
发文量
1467
审稿时长
2 months
期刊介绍: Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.
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