Synthesis of Novel Annulated Hymenialdisine Analogues via Palladium-Catalyzed Cross-Coupling Reactions with Aryl Boronic Acids

被引：4
|
作者：
Mangu, Naveenkumar [1 ,2 ]
Spannenberg, Anke [1 ]
Beller, Matthias [1 ,2 ]
Tse, Man-Kin [1 ,2 ]
机构：
[1] Univ Rostock, Leibniz Inst Katalyse eV, D-18059 Rostock, Germany
[2] Univ Rostock, Ctr Life Sci Automat CELISCA, D-18119 Rostock, Germany
来源：
SYNLETT | 2010年 / 02期
关键词：
hymenialdisine analogues; cross-coupling; silica gel; palladium; heterocycles; ASYMMETRIC EPOXIDATION; EFFICIENT SYNTHESIS; HYDROGEN-PEROXIDE; AROMATIC ALKENES; SOLVENT-FREE; OLEFINS; INHIBITION; KINASES; H2O2;
D O I：
10.1055/s-0029-1218573
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
Palladium-catalyzed Suzuki cross-coupling reactions of an indole vinyl triflate provides an efficient pathway for the synthesis of a diverse class of novel hymenialdisine analogues.
引用
收藏
页码：211 / 214
页数：4
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