Selective Synthesis of Alkynylated Isoquinolines and Biisoquinolines via Rh III Catalyzed C-H Activation/1,3-Diyne Strategy

Described herein is a convenient and highly selective synthesis of alkynylated isoquinolines and biisoquinolines from various aryl ketone O-pivaloyloxime derivatives and 1,3-diynes via rhodium-catalyzed C-H bond activation. In this transformations, alkynylated isoquinolines, 3,4'- and 3,3'...

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Veröffentlicht in:Journal of organic chemistry 2017-10, Vol.82 (19), p.10408-10417
Hauptverfasser: Feng, Ruokun, Ning, Hanqi, Su, Han, Gao, Yuan, Yin, Haotian, Wang, Yudan, Yang, Zhen, Qi, Chenze
Format: Artikel
Sprache:eng
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Zusammenfassung:Described herein is a convenient and highly selective synthesis of alkynylated isoquinolines and biisoquinolines from various aryl ketone O-pivaloyloxime derivatives and 1,3-diynes via rhodium-catalyzed C-H bond activation. In this transformations, alkynylated isoquinolines, 3,4'- and 3,3'-biisoquinolines could be obtained respectively through changing the reaction conditions. Mechanistic investigation revealed that the C-H activation of aryl ketone O-pivaloyloxime was the key step to this reaction.
ISSN:0022-3263
1520-6904
DOI:10.1021/acs.joc.7b01867