Asymmetric Aza Friedel–Crafts Reaction of 3,4-Dihydroisoquinolines with 1‑Naphthols Catalyzed by Chiral Phosphoric Acids

An efficient chiral phosphoric acid-catalyzed asymmetric aza Friedel–Crafts reaction of 3,4-dihydroisoquinolines and 1-naphthols is described. The reaction provides a general method for the synthesis of diverse chiral tetrahydroisoquinoline with 1-naphthol substituents at the C1-position in excellen...

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Veröffentlicht in:Journal of organic chemistry 2024-11, Vol.89 (21), p.15553-15558
Hauptverfasser: Zhang, Ye, Gan, Qiaoyu, Zhang, Xujin, Dai, Xiandong, Meng, Fanhua, Gao, Zhenhua, Si, Yujun, Guo, Yongbiao
Format: Artikel
Sprache:eng
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Zusammenfassung:An efficient chiral phosphoric acid-catalyzed asymmetric aza Friedel–Crafts reaction of 3,4-dihydroisoquinolines and 1-naphthols is described. The reaction provides a general method for the synthesis of diverse chiral tetrahydroisoquinoline with 1-naphthol substituents at the C1-position in excellent yields and enantioselectivities. Based on the conducted mechanistic experiments, a plausible catalytic mechanism was proposed. Moreover, the practicability of the reaction is successfully demonstrated by its application on a gram scale.
ISSN:0022-3263
1520-6904
1520-6904
DOI:10.1021/acs.joc.4c01617