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Enantioselective Amine-Catalyzed [4 + 2] Annulations of Allene Ketones and 2,3-Dioxopyrrolidine Derivatives: Synthesis of 4<i>H</i>‑Pyran Derivatives

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NIAID Data Ecosystem2026-03-08 收录
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https://figshare.com/articles/dataset/Enantioselective_Amine_Catalyzed_4_2_Annulations_of_Allene_Ketones_and_2_3_Dioxopyrrolidine_Derivatives_Synthesis_of_4_i_H_i_Pyran_Derivatives/2148832
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资源简介:
An efficient cinchona alkaloid-derived amine catalyzed asymmetric [4 + 2] cycloaddition is successfully developed. 4H-Pyran fused pyrrolin-2-one products are readily obtained in moderate to high yields with good enantioselectivites by employing allene ketones and 2,3-dioxopyrrolidine derivatives as substrates.
创建时间:
2016-02-13
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