Dasgupta, Ayan, Stefkova, Katarína, Babaahmadi, Rasool, Gierlichs, Lukas, Ariafard, Alireza and Melen, Rebecca ORCID: https://orcid.org/0000-0003-3142-2831 2020. Triarylborane-catalysed alkenylation reaction of aryl esters with diazo compounds. Angewandte Chemie International Edition 59 (36) , pp. 15492-15496. 10.1002/anie.202007176 |
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Official URL: http://dx.doi.org/10.1002/anie.202007176
Abstract
Herein we report a facile, mild reaction protocol to form carbon‐carbon bonds in the absence of transition metal catalysts. We demonstrate the metal‐free alkenylation reactions of aryl esters with α‐diazoesters to give highly functionalized enyne products. Catalytic amounts of tris(pentafluorophenyl)borane (10–20 mol%) are employed to afford the C=C coupled products (31 examples) in good to excellent yields (36–87%). DFT studies have been undertaken to elucidate the mechanism for this alkenylation reaction.
Item Type: | Article |
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Date Type: | Publication |
Status: | Published |
Schools: | Chemistry Cardiff Catalysis Institute (CCI) |
Publisher: | Wiley |
ISSN: | 1433-7851 |
Funders: | EPSRC |
Date of First Compliant Deposit: | 15 June 2020 |
Date of Acceptance: | 2 June 2020 |
Last Modified: | 25 Jul 2024 13:14 |
URI: | https://orca.cardiff.ac.uk/id/eprint/132446 |
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