Diversity-oriented synthesis of imidazo[2,1-a]isoquinolines
Annulation
DOI:
10.1039/c8cc05390a
Publication Date:
2018-07-19T10:35:30Z
AUTHORS (7)
ABSTRACT
Herein, we report an efficient and practical strategy for the synthesis of five types imidazo[2,1-<italic>a</italic>]isoquinolines <italic>via</italic> Cp*Rh<sup>III</sup>-catalyzed [4+2] annulation 2-arylimidazoles α-diazoketoesters, whose structural substituted diversity at 5- or 6-position can be precisely controlled by α-diazoketoester coupling partners.
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