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Toward a mild dehydroformylation using base-metal catalysis

Author(s): Abrams, Dylan J.; West, Julian G.; Sorensen, Erik J.

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dc.contributor.authorAbrams, Dylan J.-
dc.contributor.authorWest, Julian G.-
dc.contributor.authorSorensen, Erik J.-
dc.date.accessioned2020-10-30T19:05:21Z-
dc.date.available2020-10-30T19:05:21Z-
dc.date.issued2017en_US
dc.identifier.citationAbrams, Dylan J, West, Julian G, Sorensen, Erik J. (2017). Toward a mild dehydroformylation using base-metal catalysis. Chemical Science, 8 (3), 1954 - 1959. doi:10.1039/C6SC04607Jen_US
dc.identifier.issn2041-6520-
dc.identifier.urihttp://arks.princeton.edu/ark:/88435/pr1tv5j-
dc.description.abstractDehydroformylation, or the reaction of aldehydes to produce alkenes, hydrogen gas, and carbon monoxide, is a powerful transformation that is underdeveloped despite the high industrial importance of the reverse reaction, hydroformylation. Interestingly, nature routinely performs a related transformation, oxidative dehydroformylation, in the biosynthesis of cholesterol and related sterols under mild conditions using base-metal catalysts. In contrast, chemists have recently developed a non-oxidative dehydroformylation method; however, it requires high temperatures and a precious-metal catalyst. Careful study of both approaches has informed our efforts to design a base-metal catalyzed, mild dehydroformylation method that incorporates benefits from each while avoiding several of their respective disadvantages. Importantly, we show that cooperative base metal catalysis presents a powerful, mechanistically unique approach to reactions which are difficult to achieve using conventional catalyst design.en_US
dc.format.extent1954 - 1959en_US
dc.language.isoen_USen_US
dc.relation.ispartofChemical Scienceen_US
dc.rightsFinal published version. This is an open access article.en_US
dc.titleToward a mild dehydroformylation using base-metal catalysisen_US
dc.typeJournal Articleen_US
dc.identifier.doidoi:10.1039/C6SC04607J-
dc.date.eissued2017en_US
dc.identifier.eissn2041-6539-
pu.type.symplectichttp://www.symplectic.co.uk/publications/atom-terms/1.0/journal-articleen_US

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