Concise synthesis of pyrrolophenanthridine alkaloids using a Pd-mediated biaryl coupling reaction with regioselective C-H activation via the intramolecular coordination of the amine to Pd

被引:47
作者
Harayama, T [1 ]
Hori, A [1 ]
Abe, H [1 ]
Takeuchi, Y [1 ]
机构
[1] Okayama Univ, Fac Pharmaceut Sci, Okayama 7008530, Japan
关键词
coodination; palladium; regioselectivity; anhydrolycorine; assoanine;
D O I
10.1016/j.tet.2003.11.093
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The concise synthesis of Amaryllidaceae alkaloids, such as anhydrolycorinone, anhydrolycorin-7-one, assoanine, and oxoassoanine, which have a pyrrolophenanthridine skeleton, was achieved in moderate yield using the Pd-mediated biaryl coupling reaction of 1-(2-halobenzyl)-2,3-dihydroindole, which applied the regioselective C-H activation method with intramolecular coordination of the benzylamino group to Pd. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1611 / 1616
页数:6
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