
Tetrahedron (2021)
Update date:2022-08-02
Topics:
Shibasaki, Kaho
Togo, Hideo
Treatment of aryl 2-iodophenyl ketones with TMS2NH in the presence of Sc(OTf)3 at warming conditions, followed by the reaction with styrenes and NIS gave N-(1-aryl-2-iodoethyl) aryl 2-iodophenyl ketimines. Further treatment of N-(1-aryl-2-iodoethyl) aryl 2-iodophenyl ketimines with tBuOK in the presence of 1,10-phenanthroline at 120 °C generated 1,3-diarylisoquinolines in moderate yields through SET from tBuOK onto the iodophenyl group to form aryl radicals, their 6-endo-trig cyclization onto the vinyl groups, and aromatization of the cyclized intermediates. The present method is a novel approach for the preparation of the isoquinoline core via two steps from aryl 2-iodophenyl ketones.
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Doi:10.1021/ol100161n
(2010)Doi:10.1021/cc900157w
(2010)Doi:10.1016/j.tetasy.2010.01.020
(2010)Doi:10.1021/ol026761j
(2002)Doi:10.1039/c0ob00592d
(2011)Doi:10.1016/j.ejmech.2009.12.051
(2010)