4.7 Article

Catalyst-controlled synthesis of 4-amino-isoquinolin-1(2H)-one and oxazole derivatives

期刊

ORGANIC CHEMISTRY FRONTIERS
卷 5, 期 9, 页码 1466-1470

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c8qo00125a

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资金

  1. National Basic Research Program of China (973) [2015CB856603]
  2. Chinese Academy of Sciences [XDB20000000, sioczz201808]
  3. National Natural Science Foundation of China [20472096, 21372241, 21572052, 20672127, 21421091, 21372250, 21121062, 21302203, 20732008, 21772037, 21772226]
  4. Fundamental Research Funds for the Central Universities [222201717003]

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A facile synthetic method to access 4-amino-isoquinolin-1(2H)-one and oxazole derivatives was disclosed in this paper. The reaction of N-(pivaloyloxy)-amides with ynamides produced 4-amino-isoquinolin-1(2H)-ones in good yields in the presence of (CpRh)-Rh-star(III) catalyst through a C-H bond functionalization. Using Sc(OTf)(3) as the catalyst, oxazole derivatives were obtained in good yields from the same reaction. This protocol features good functional group tolerance and excellent regioselectivity.

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