کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1254565 | 971381 | 2016 | 6 صفحه PDF | دانلود رایگان |

2-Amino-3-nitrile-chromenes with potential antitumor activity were constructed by a novel catalytic system. In combination with α-naphthol, quinine could effectively promote the Michael-cyclization process of malononitrile with functionalized chalcones in high yields and moderate to good enantioselectivity (up to 84% ee). It is notable that the enantioselectivity could be greatly improved when α-naphthol was employed as additive.
The natural cinchona alkaloid quinine could efficiently promote a tandem conversion of chalcones and 2-amino-3-nitrile-chromenes were furnished in high yields (75%–99%) and moderate to good enantioselectivity (49%–84% ee). In particularly, achiral α-naphthol exerted a positive impact on the stereoselectivity and a significant enantioselectivity improvement was observed.Figure optionsDownload as PowerPoint slide
Journal: Chinese Chemical Letters - Volume 27, Issue 1, January 2016, Pages 25–30