| Literature DB >> 28378401 |
Mária Bakos1, Ádám Gyömöre1, Attila Domján1, Tibor Soós1.
Abstract
Herein we report that a single frustrated Lewis pair (FLP) catalyst can promote the reductive etherification of aldehydes and ketones. The reaction does not require an exogenous acid catalyst, but the combined action of FLP on H2 , R-OH or H2 O generates the required Brønsted acid in a reversible, "turn on" manner. The method is not only a complementary metal-free reductive etherification, but also a niche procedure for ethers that would be either synthetically inconvenient or even intractable to access by alternative synthetic protocols.Entities:
Keywords: boranes; catalysis; frustrated Lewis pairs; hydrogenation; reductive etherification
Year: 2017 PMID: 28378401 DOI: 10.1002/anie.201700231
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336