Metal-Free Activation of a C(sp)−H Bond of Aryl Acetylenes

C(sp)−H Bond activation of acetylene molecule still remains a challenge for synthetic organic chemists. In practice, acetylenes are activated by strong bases and metals. The first example for activating acetylenic protons under base and metal‐free conditions is reported here. It involves a general m...

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Veröffentlicht in:Chemistry : a European journal 2016-10, Vol.22 (42), p.14812-14815
Hauptverfasser: Rout, Laxmidhar, Parida, Bibhuti Bhusan, Florent, Jean-Claude, Johannes, Ludger, Choudhury, Santosh Kumar, Phaomei, Ganngam, Scanlon, Joe, Bertounesque, Emmanuel
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Sprache:eng
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Zusammenfassung:C(sp)−H Bond activation of acetylene molecule still remains a challenge for synthetic organic chemists. In practice, acetylenes are activated by strong bases and metals. The first example for activating acetylenic protons under base and metal‐free conditions is reported here. It involves a general method for synthesizing propargylic derivatives of cotarnine. An array of tetrahydroisoquinolines alkaloids was synthesized by C(sp)−H bond activation of aromatic acetylenes with cotarnine at room temperature. A DFT‐based mechanism is proposed for the reaction. Virgin C−H bonds: The first example for activating acetylenic protons under base‐ and metal‐free conditions is reported. This includes a general method for synthesizing propargylic derivatives of cotarnine. An array of tetrahydroisoquinolines alkaloids was synthesized by C−C bond formation between cotarnine and aryl acetylenes at room temperature. A DFT‐based mechanism is proposed for the reaction.
ISSN:0947-6539
1521-3765
DOI:10.1002/chem.201603003