Have you ever imagined reactions of alkenes with hydrogen that result in anything other than hydrogenation or hydrogenative C-C coupling? We have long sought to develop not only hydrogenation catalysts that activate H as hydride ions but also electron transfer catalysts that activate H as a direct electron donor. Here, we report the reductive cyclopropanation of alkenes using an iridium electron storage catalyst with H as the electron source without releasing metal waste from the reductant. We discuss the catalytic mechanism with selectivity to give the -isomer. These findings are based on the isolation of three complexes and density functional theory calculations.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11040560 | PMC |
http://dx.doi.org/10.1021/jacsau.4c00098 | DOI Listing |
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