<P>An efficient and practical method for the direct cross-coupling between quinolones and a range of azoles was developed <I>via</I> copper-mediated C–H functionalization. This synthetic strategy provides a convenient access to...
http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
https://www.riss.kr/link?id=A107553975
2014
-
SCI,SCIE,SCOPUS
학술저널
5719-5726(8쪽)
0
상세조회0
다운로드다국어 초록 (Multilingual Abstract)
<P>An efficient and practical method for the direct cross-coupling between quinolones and a range of azoles was developed <I>via</I> copper-mediated C–H functionalization. This synthetic strategy provides a convenient access to...
<P>An efficient and practical method for the direct cross-coupling between quinolones and a range of azoles was developed <I>via</I> copper-mediated C–H functionalization. This synthetic strategy provides a convenient access to a variety of C3-heteroaryl quinolones, quinolinone, nalidixic acid, uracil, pyridone and chromone derivatives, which are prominent structural motifs in many biologically active compounds.</P>
<P>Graphic Abstract</P><P>An efficient and practical method for the direct cross-coupling between quinolones and a range of azoles was developed <I>via</I> copper-mediated C–H functionalization.
<IMG SRC='http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=c4ob00939h'>
</P>
Efficient synthesis of mibefradil analogues: an insight into in vitro stability