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Synthesis 2021; 53(18): 3290-3298
DOI: 10.1055/a-1521-5800
DOI: 10.1055/a-1521-5800
special topic
Bond Activation – in Honor of Prof. Shinji Murai
Cobalt-Catalyzed Oxidative [4+2] Annulation of Benzamides with Dihydrofuran: A Facile Route to Tetrahydrofuro[2,3-c]isoquinolinones
This work was supported by Chengdu University (2081919140) and Outstanding Young Talents of Zhejiang Province High Level Personnel of Special Support (ZJWR0108).
Abstract
A cobalt-catalyzed oxidative [4+2] annulation of benzamides with dihydrofuran was developed for the expeditious synthesis of tetrahydrofuro[2,3-c]isoquinolinones. Commercially available and inexpensive Co(OAc)2·4H2O was used as an efficient catalyst. Various functional groups were tolerated, affording the desired products in good yields with excellent regioselectivity and good diastereoselectivity under mild conditions.
Key words
cobalt - oxidative annulations - C–H activation - tetrahydrofuro[2,3-c]isoquinolinone - dihydrofuranSupporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/a-1521-5800.
- Supporting Information
Publication History
Received: 08 May 2021
Accepted after revision: 01 June 2021
Accepted Manuscript online:
01 June 2021
Article published online:
24 June 2021
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For the pioneering development of bidentate directing groups, see:
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For selected reviews, see: