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Synthesis 2020; 52(11): 1625-1633
DOI: 10.1055/s-0039-1690866
DOI: 10.1055/s-0039-1690866
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Cobalt(III)-Catalyzed Redox-Neutral Coupling of Acrylamides with Activated Alkenes via C–H Bond Activation
We thank the Department of Science and Technology, Science and Engineering Research Board (DST-SERB, CRG/2018/000606), India for the support of this research. M.S.K. thanks the Indian Institute of Technology Madras (IITM) for an HTRA Fellowship.Further Information
Publication History
Received: 18 December 2019
Accepted after revision: 04 March 2020
Publication Date:
30 March 2020 (online)
We would like to dedicate this work to Prof. Chien-Hong Cheng on the occasion of his 70th birthday.
Abstract
A cobalt(III)-catalyzed coupling of substituted acrylamides with maleimides in the presence of 30 mol% pivalic acid providing olefin-migrated succinimide derivatives in a redox-neutral manner is described. The coupling reaction was examined with various substituted acrylamides and maleimides. The scope of the C–H alkylation reaction was also examined with substituted acrylates. A possible reaction mechanism involving a five-membered cobaltocycle as a key intermediate is proposed.
Key words
acrylamides - maleimides - C–H activation - alkylation - succinimides - acrylates - cobaltSupporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/s-0039-1690866.
- Supporting Information
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