Controlling chemoselectivity in copper-catalyzed decarboxylative A3/A3 cross-couplings: direct formation of unsymmetrical 1,4-diamino-2-butynes

Literature Information

Publication Date 2016-10-10
DOI 10.1039/C6QO00499G
Impact Factor 5.281
Authors

Panfeng Zhao, Huangdi Feng, Haoran Pan, Zhihua Sun, Minchao Tong


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Abstract

A direct cross-coupling of propiolic acid with two kinds of in situ formed iminiums has been achieved via the CuI/CuCl2-catalyzed decarboxylative A3/A3 domino process. This novel protocol to synthesise unsymmetrical 1,4-diamino-2-butynes is operationally simple in an atom- and step-economical manner, and provides products in moderate to excellent yields with high chemoselectivity.

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DOI: 10.1039/C0CP90038A

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DOI: 10.1039/C0CP90052D

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