Trans-Selective and Switchable Arene Hydrogenation of Phenol Derivatives

Wollenburg M., Heusler A., Bergander K., Glorius F.

Research article (journal) | Peer reviewed

Abstract

A trans-selective arene hydrogenation of abundant phenol derivatives catalyzed by a commercially available heterogeneous palladium catalyst is reported. The described method tolerates a variety of functional groups and provides access to a broad scope of trans-configurated cyclohexanols as potential building blocks for life sciences and beyond in a one-step procedure. The transformation is strategically important because arene hydrogenation preferentially delivers the opposite cis-isomers. The diastereoselectivity of the phenol hydrogenation can be switched to the cis-isomers by employing rhodium-based catalysts. Moreover, a protocol for the chemoselective hydrogenation of phenols to cyclohexanones was developed.

Details about the publication

JournalACS Catalysis
Volume10
Issue19
Page range11365-11370
StatusPublished
Release year2020
Language in which the publication is writtenEnglish
DOI10.1021/acscatal.0c03423
Link to the full texthttps://api.elsevier.com/content/abstract/scopus_id/85096351606
Keywordscyclohexanols; palladium catalysis; arene hydrogenation; switchability; trans-selective

Authors from the University of Münster

Bergander, Klaus
Organic Chemistry Institute