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Lewis Acid and (Hypo)iodite Relay Catalysis Allows a Strategy for the Synthesis of Polysubstituted Azetidines and Tetrahydroquinolines

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NIAID Data Ecosystem2026-03-09 收录
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https://figshare.com/articles/dataset/Lewis_Acid_and_Hypo_iodite_Relay_Catalysis_Allows_a_Strategy_for_the_Synthesis_of_Polysubstituted_Azetidines_and_Tetrahydroquinolines/4003983
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资源简介:
A catalytic [3 + 1]-annulation reaction between cyclopropane 1,1-diester and aromatic amine is developed based on the relay catalysis strategy. Lewis acid-catalyzed nucleophilic ring opening of cyclopropane 1,1-diester with aromatic amine and (hypo)­iodite-catalyzed C–N bond formation are combined successfully in one reaction. Using this reaction, biologically important azetidines and tetrahydroquinolines can be prepared directly.
创建时间:
2016-10-17
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