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Synthesis of Aporphine Analogues via Palladium-Catalyzed Intramolecular Aryl–Aryl Dehydrogenative Coupling
The Journal of Organic Chemistry ( IF 3.3 ) Pub Date : 2021-09-09 , DOI: 10.1021/acs.joc.1c01649
Chen Su 1 , Wen-Hua Xu 1 , Rui-Li Guo 1 , Xing-Long Zhang 1 , Xue-Qing Zhu 1 , Ya-Ru Gao 1 , Yong-Qiang Wang 1
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Reported herein is an intramolecular dehydrogenative coupling of two inert aryl C–H bonds for the synthesis of aporphine analogues. The process represents a novel tool for the preparation of aporphines via palladiun-catalyzed C–H bond activation. The present reaction is compatible with various functional groups, and the coupling products have been further applied for the synthesis of natural products aporphine and zenkerine.

中文翻译:

通过钯催化的分子内芳基-芳基脱氢偶联合成阿朴啡类似物

本文报道了用于合成阿朴啡类似物的两个惰性芳基 C-H 键的分子内脱氢偶联。该过程代表了一种通过钯催化的 C-H 键活化制备阿朴啡的新工具。本反应与多种官能团相容,偶联产物已进一步应用于天然产物阿朴啡和zenkerine的合成。
更新日期:2021-10-01
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