Highly Selective Synergistic Copper(I/II)‐Catalyzed A3 Cross Coupling/Decarboxylative A3 Domino Reactions in Water

A microwave‐assisted copper‐catalyzed A3 cross‐coupling/decarboxylative A3 domino reaction of a propiolic acid, an aldehyde, a formaldehyde solution and an amine is described. This strategy represents the first one‐pot cross‐coupling reaction for the direct synthesis of trisubstituted unsymmetrical...

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Veröffentlicht in:Asian journal of organic chemistry 2017-02, Vol.6 (2), p.161-164
Hauptverfasser: Feng, Huangdi, Zhao, Panfeng, Huang, Liliang, Sun, Zhihua, Tong, Minchao
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Sprache:eng
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Zusammenfassung:A microwave‐assisted copper‐catalyzed A3 cross‐coupling/decarboxylative A3 domino reaction of a propiolic acid, an aldehyde, a formaldehyde solution and an amine is described. This strategy represents the first one‐pot cross‐coupling reaction for the direct synthesis of trisubstituted unsymmetrical 2‐butynes with a broad functional group tolerance in good yields (up to 91 %) and excellent chemoselectivity. The simultaneous activation of both the C−COOH and C−H bond of propiolic acid is crucial in this approach, and only carbon dioxide and water are generated as byproducts. A microwave‐assisted copper‐catalyzed A3 cross‐coupling/decarboxylative A3 domino reaction of a propiolic acid, an aldehyde, a formaldehyde solution and an amine has been reported resulting in trisubstituted unsymmetrical 2‐butynes in good yields.
ISSN:2193-5807
2193-5815
DOI:10.1002/ajoc.201600524