A new facile synthesis of 3-amidoindole derivatives and their evaluation as potential GSK-3β inhibitors

被引:57
作者
Pews-Davtyan, Anahit [2 ]
Tillack, Annegret [2 ]
Schmoele, Anne-Caroline [1 ]
Ortinau, Stefanie [1 ]
Frech, Moritz J. [1 ]
Rolfs, Arndt [1 ]
Beller, Matthias [2 ]
机构
[1] Univ Rostock, Albrecht Kossel Inst Neuroregenerat, Ctr Mental Hlth Dis, D-18147 Rostock, Germany
[2] Univ Rostock, Leibniz Inst Katalyse eV, D-18059 Rostock, Germany
关键词
ONE-POT SYNTHESIS; INTRAMOLECULAR HYDROAMINATION; INTERMOLECULAR HYDROAMINATION; TERMINAL ALKYNES; DOMINO SYNTHESIS; CATALYTIC HYDROAMINATION; BIOLOGICAL EVALUATION; CONVENIENT SYNTHESIS; REDUCTIVE ACYLATION; SUBSTITUTED INDOLES;
D O I
10.1039/b920861e
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
3-Amidoindoles were synthesized from commercially available arylhydrazines and propargylamines over Zn-salt mediated one pot procedure in excellent regioselectivity and up to 94% yield.
引用
收藏
页码:1149 / 1153
页数:5
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