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Cobalt Catalyst Determines Regioselectivity in Ring Opening of Epoxides with Aryl Halides.
| Content Provider | Europe PMC |
|---|---|
| Author | Potrząsaj, Aleksandra Musiejuk, Mateusz Chaładaj, Wojciech Giedyk, Maciej Gryko, Dorota |
| Copyright Year | 2021 |
| Abstract | Ring-opening of epoxidesfurnishing either linear or branched productsbelongs to the group of classic transformations in organic synthesis.However, the regioselective cross-electrophile coupling of aryl epoxideswith aryl halides still represents a key challenge. Herein, we reportthat the vitamin B12/Ni dual-catalytic system allows forthe selective synthesis of linear products under blue-light irradiation,thus complementing methodologies that give access to branched alcohols.Experimental and theoretical studies corroborate the proposed mechanisminvolving alkylcobalamin as an intermediate in this reaction. |
| ISSN | 00027863 |
| Volume Number | 143 |
| PubMed Central reference number | PMC8297733 |
| Issue Number | 25 |
| PubMed reference number | 34081860 |
| Journal | Journal of the American Chemical Society [J. Am. Chem. Soc] |
| e-ISSN | 15205126 |
| DOI | 10.1021/jacs.1c00659 |
| Language | English |
| Publisher | American ChemicalSociety |
| Publisher Date | 2021-06-03 |
| Access Restriction | Open |
| Rights License | Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). © 2021 The Authors. Publishedby AmericanChemical Society |
| Content Type | Text |
| Resource Type | Article |
| Subject | Chemistry Colloid and Surface Chemistry Biochemistry Catalysis |