2023
DOI: 10.1039/d3gc02326e
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CO2-facilitated radical sequential (3 + 2) annulation of 1,6-enynes via cooperation of sulfinate catalysis and photocatalysis

Abstract: Reported here is the CO2-facilitated radical sequential (3+2) annulation of 1,6-enynes that proceeds under the concerted catalysis of sulfinate and photocatalyst (PC) to construct benzo-fused tricyclic scaffolds, that is, tetrahydrofluorenes...

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Cited by 6 publications
(1 citation statement)
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References 86 publications
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“…According to previous literature, 10 a ,15 the reaction might undergo oxidative addition of H 2 O with Ni(0) to form a stable Ni–OH bond and constrained the reaction. Inspired by previous studies on CO 2 promoted reactions, 16 we assumed that CO 2 might convert the hydroxyl group into an easy leaving bicarbonate group, which accelerated the reaction.…”
mentioning
confidence: 99%
“…According to previous literature, 10 a ,15 the reaction might undergo oxidative addition of H 2 O with Ni(0) to form a stable Ni–OH bond and constrained the reaction. Inspired by previous studies on CO 2 promoted reactions, 16 we assumed that CO 2 might convert the hydroxyl group into an easy leaving bicarbonate group, which accelerated the reaction.…”
mentioning
confidence: 99%