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Rhodium-Catalyzed Regio‑, Diastereo‑, and Enantioselective Three-Component Carboamination of Dienes via C–H Activation

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acs.figshare.com2023-06-05 更新2025-01-21 收录
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https://acs.figshare.com/articles/dataset/Rhodium-Catalyzed_Regio_Diastereo_and_Enantioselective_Three-Component_Carboamination_of_Dienes_via_C_H_Activation/14663605/1
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Reported herein is the rhodium-catalyzed enantioselective three-component coupling of arene, diene, and dioxazolone that occurs via C–H activation en route to allyl intermediate. This carboamination reaction affords chiral allylic amines in 1,2-selectivity, E-selectivity, and enantioselectivity, with electrophilic amination of the π-allyl species being both regio- and enantio-determining.

本文报道了一种通过C-H活化途径至烯丙基中间体的过程中发生的钯催化、手性选择性的三组分偶联反应,该反应涉及芳烃、二烯和二氧杂唑酮。该羰基氨化反应能够以1,2选择性、E选择性和对映选择性合成手性烯丙基胺,其中π-烯丙基物种的亲电氨化反应同时决定了区域选择性和对映选择性。
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