通过Friedel-Crafts烷基化/环化不对称合成7-元环桥3,4-氟三环吲哚†

Bai-Yu Xue , Chen-Ying Hou , Xiao-Bing Wang , Ming-Sheng Xie , Hai-Ming Guo
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引用次数: 0

摘要

以N-甲基-4-氨基吲哚为1,4-双亲核试剂,用5mol%Ni(ii)-PyBPI配合物报道了与β,γ-不饱和α-酮酯的区域和对映选择性Friedel–Crafts烷基化/N-半缩醛化和脱水序列,得到了各种手性的7-元环桥3,4-氟三环吲哚,结果良好(产率高达91%,ee高达97%)。副产物是6-元环桥4,5-氟三环吲哚。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Asymmetric synthesis of 7-membered-ring-bridged 3,4-fused tricyclic indoles via Friedel–Crafts alkylation/annulation†

Asymmetric synthesis of 7-membered-ring-bridged 3,4-fused tricyclic indoles via Friedel–Crafts alkylation/annulation†

With N-methyl-4-aminoindole as the 1,4-bisnucleophile, the regio- and enantioselective Friedel–Crafts alkylation/N-hemiacetalization and dehydration sequence with β,γ-unsaturated α-ketoesters was reported using 5 mol% Ni(ii)-PyBPI complex, affording diverse chiral 7-membered-ring-bridged 3,4-fused tricyclic indoles in good results (up to 91% yield and 97% ee). The by-products were 6-membered-ring-bridged 4,5-fused tricyclic indoles.

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