Visible light promoted metal and oxidant-free stereoselective synthesis of functionalized succinimides from aza-1,6-enynes†

Shivam A. Meena, Deepika Thakur, Debanik Panda, Rahul Ranjan and Akhilesh K. Verma
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Abstract

An operationally simple approach has been developed for synthesizing diversely functionalized succinimides under transition-metal and oxidant-free conditions in PEG-400. The developed strategy is promoted by visible light and proceeds via radical cascade iodo-sulfonylation of aza-1,6-enynes in an atom atom-economical manner with excellent stereoselectivity. Control experiments well support the proposed pathway for the reaction. The reaction's expedient features include operational simplicity, eco-friendly solvent, atom economy, and functional group tolerance with a broad substrate scope.

Abstract Image

可见光促进了偶氮-1,6-炔†的金属和无氧化剂立体选择性合成功能化琥珀酰亚胺
在过渡金属和无氧化剂条件下,在PEG-400中合成了一种操作简单的不同功能化琥珀酰亚胺。在可见光的催化下,氮杂-1,6-炔的碘磺酰化反应以原子-原子经济的方式进行,具有良好的立体选择性。对照实验很好地支持了所提出的反应途径。该反应具有操作简单、溶剂环保、原子经济、官能团耐受性好、底物范围广等优点。
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0.60
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