Cobalt-catalysed alkene hydrogenation: a metallacycle can explain the hydroxyl activating effect and the diastereoselectivity. Issue 22 (11th May 2018)

• Record Type: Journal Article
• Authors: Morello, Glenn R.; Zhong, Hongyu; Chirik, Paul J.; Hopmann, Kathrin H.
• Is Part Of: Chemical science. Volume 9:Issue 22(2018)
• Page Start: 4977
• Page End: 4982
• Publication Date: 2018-05-11
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c8sc01315b
• Languages: English
• ISSNs: 2041-6520

Abstract

Abstract : A new non-redox metallacycle mechanism explains the substrate preference, the diastereoselectivity, and the hydroxyl activating effect in cobalt-catalyzed alkene hydrogenation. Abstract : Bis(phosphine)cobalt dialkyl complexes have been reported to be highly active in the hydrogenation of tri-substituted alkenes bearing hydroxyl substituents. Alkene substrates containing ether, ester, or ketone substituents show minimal reactivity, indicating an activating effect of the hydroxyl group. The mechanistic details of bis(phosphine)cobalt-catalysed hydrogenation were recently evaluated computationally (X. Ma, M. Lei, J. Org. Chem. 2017, 82, 2703–2712) and a Co(0)–Co(ii ) redox mechanism was proposed. However, the activating effect of the hydroxyl substituent and the accompanying high diastereoselectivity were not studied. Here we report a computational study rationalizing the role of the hydroxyl group through a key metallacycle species. The metallacycle is part of a non-redox catalytic pathway proceeding through Co(ii ) intermediates throughout. The preference for alcohol over ether substrates and the high diastereoselectivity of terpinen-4-ol hydrogenation are correctly predicted in computations adopting the new pathway, whereas the alternative redox mechanism predicts ethers rather than alcohols to be more reactive substrates. Additional experimental evidence supports the role of the hydroxyl group in the metallacycle mechanism. Our work highlights the importance of employing known substrate preferences and stereoselectivities to test the validity of computationally proposed reaction pathways.