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Rh(iii)-catalyzed synthesis of tetracyclic isoquinolinium salts via C-H activation and [4+2] annulation of 1-phenyl-3,4-dihydroisoquinolines and alkynes in ethanol.


ABSTRACT: An efficient and convenient method to construct tetracyclic isoquinolinium salts via [Cp*RhCl2]2 catalyzed C-H activation and [4 + 2] annulation reactions in ethanol is described. This reaction is very fast and highly efficient in the green solvent ethanol. The reaction works with a broad substrate scope affording the products in good to excellent yields in a short time. Moreover, a ratio of S/C up to 10 000 could be achieved with gram scale synthesis.

SUBMITTER: Dang X 

PROVIDER: S-EPMC9085511 | biostudies-literature | 2018 Aug

REPOSITORIES: biostudies-literature

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Rh(iii)-catalyzed synthesis of tetracyclic isoquinolinium salts <i>via</i> C-H activation and [4+2] annulation of 1-phenyl-3,4-dihydroisoquinolines and alkynes in ethanol.

Dang Xinxin X   He Yu Y   Liu Yingtian Y   Chen Xuehong X   Li Jun-Long JL   Zhou Xian-Li XL   Jiang Hezhong H   Li Jiahong J  

RSC advances 20180824 52


An efficient and convenient method to construct tetracyclic isoquinolinium salts <i>via</i> [Cp*RhCl<sub>2</sub>]<sub>2</sub> catalyzed C-H activation and [4 + 2] annulation reactions in ethanol is described. This reaction is very fast and highly efficient in the green solvent ethanol. The reaction works with a broad substrate scope affording the products in good to excellent yields in a short time. Moreover, a ratio of S/C up to 10 000 could be achieved with gram scale synthesis. ...[more]

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