Direct Mannich and nitro-Mannich reactions with non-activated imines:: AgOTf-catalyzed addition of pronucleophiles to ortho-alkynylaryl aldimines leading to 1,2-dihydroisoquinolines

被引:218
作者
Asao, N [1 ]
Yudha, S [1 ]
Nogami, T [1 ]
Yamamoto, Y [1 ]
机构
[1] Tohoku Univ, Grad Sch Sci, Dept Chem, Sendai, Miyagi 9808578, Japan
关键词
imines; Mannich reaction; nitrogen heterocycles; pronucleophiles; synthetic methods;
D O I
10.1002/anie.200500795
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
(Chemical Equation Presented) A variety of 1,2-dihydroisoquinoline derivatives 3 have been prepared in good to high yields by the AgOTf-catalyzed reaction of ortho-alkynylaryl aldimines 1 with various pronucleophiles 2 (see scheme). Treatment of 1 with a stoichiometric amount of AgOTf followed by protonation with TfOH produced 4, which suggests the formation of an isoquinolinium intermediate in the present direct addition reaction. Tf=trifluoromethanesulfonyl. © 2005 Wiley-VCH Verlag GmbH & Co. KGaA.
引用
收藏
页码:5526 / 5528
页数:3
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