| Literature DB >> 29874413 |
Fábio M S Rodrigues1, Peter K Kucmierczyk2,3, Marta Pineiro1, Ralf Jackstell2, Robert Franke3,4, Mariette M Pereira1, Matthias Beller2.
Abstract
An active and selective dual catalytic system to promote domino hydroformylation-reduction reactions is described. Apart from terminal, di- and trisubstituted olefins, for the first time the less active internal C-C double bond of tetrasubstituted alkenes can also be utilized. As an example, 2,3-dimethylbut-2-ene is converted into the corresponding n-alcohol with high yield (90 %) as well as regio- and chemoselectivity (>97 %). Key for this development is the use of a combination of Rh complexes with bulky monophosphite ligands and the Ru-based Shvo's complex. A variety of aromatic and aliphatic alkenes can be directly used to obtain mainly linear alcohols.Entities:
Keywords: alcohols; homogeneous catalysis; rhodium; ruthenium; tandem reactions
Year: 2018 PMID: 29874413 DOI: 10.1002/cssc.201800488
Source DB: PubMed Journal: ChemSusChem ISSN: 1864-5631 Impact factor: 8.928