4.5 Article

Synthesis of 1-Aminoisoquinolines via the Coinage Metal Cocatalyzed Reaction of 2-Alkynylbenzaldoximes with Isocyanoacetates

Journal

SYNTHESIS-STUTTGART
Volume 46, Issue 23, Pages 3213-3220

Publisher

GEORG THIEME VERLAG KG
DOI: 10.1055/s-0034-1378654

Keywords

1-aminoisoquinolines; coinage metals; deformylation; 2-alkynylbenzaldoximes; isocyanoacetates

Funding

  1. National Natural Science Foundation of China [21262018, 20862007, 21202065]
  2. Natural Science Foundation of Jiangxi Province [2010GZH0070]

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An efficient reaction of 2-alkynylbenzaldoximes with 2-isocyanoacetates cocatalyzed by silver triflate and gold(I) chloride is described, providing 1-aminoisoquinolines in good to excellent yields under mild conditions. Mechanistic experiments suggest that the gold(I) cation might play a crucial role in the activation of the isocyanide substrate. The observed reactivity and the unique pathway of substrate activation in the cocatalyzed processes are quite informative for further study.

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