2015
DOI: 10.1021/jacs.5b06077
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Iron-Catalyzed Reduction of CO2 into Methylene: Formation of C–N, C–O, and C–C Bonds

Abstract: We report herein the use of the (dihydrido)iron catalyst, Fe(H)2(dmpe)2, for the selective reduction of CO2 into either bis(boryl)acetal or methoxyborane depending on the hydroborane used as a reductant. In a one-pot two-step procedure, the in situ generated bis(boryl)acetal was shown to be a reactive and versatile source of methylene to create new C-N but also C-O and C-C bonds.

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Cited by 140 publications
(103 citation statements)
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“…In the course of these studies, we reported the first formation of bis(boryl)acetal . Subsequently, we described a rare selective generation of the bis(boryl)acetal 1 (Scheme b) and proved that this compound reacts as a surrogate of formaldehyde in the case of condensation processes and Wittig reaction . We report herein the first generation of asymmetric carbon centres from CO 2 , with the synthesis of a borylated C 3 carbohydrate.…”
Section: Introductionmentioning
confidence: 87%
“…In the course of these studies, we reported the first formation of bis(boryl)acetal . Subsequently, we described a rare selective generation of the bis(boryl)acetal 1 (Scheme b) and proved that this compound reacts as a surrogate of formaldehyde in the case of condensation processes and Wittig reaction . We report herein the first generation of asymmetric carbon centres from CO 2 , with the synthesis of a borylated C 3 carbohydrate.…”
Section: Introductionmentioning
confidence: 87%
“…Later the authors showed that an iron catalysed pathway involving metal hydride catalyst is also feasible for the generation of borylmethylene derivatives with good selectivities. 65 Likewise most recently in 2016, Cantat and Berthet showed that besides iron, also copper and cobalt phosphine complexes are active for the borylation of CO2 yielding mixtures of bisboryl acetal and methoxy borane with a broad range of selectivity for these two products. 66 Please do not adjust margins Please do not adjust margins Scheme 10.…”
Section: Formaldehyde Derivativesmentioning
confidence: 99%
“…5i-k, 8 Based on our interest in iron catalysis involving hydroboranes, namely hydroboration of alkenes, 12d C-H borylation of arenes, 18 and CO 2 functionalization, 19 we decided to test the newly prepared complexes in the reaction of styrene with pinacolborane (HBpin). 5i-k, 8 Based on our interest in iron catalysis involving hydroboranes, namely hydroboration of alkenes, 12d C-H borylation of arenes, 18 and CO 2 functionalization, 19 we decided to test the newly prepared complexes in the reaction of styrene with pinacolborane (HBpin).…”
Section: Characterization Of the Complexesmentioning
confidence: 99%