| Literature DB >> 28809505 |
Konrad Gebauer1, Franziska Reuß1, Matthias Spanka1, Christoph Schneider1.
Abstract
The combination of an in situ formed MnL3 complex (HL = Hacac or R(C═O)CH2CO2R) and a chiral phosphoric acid HX* allows for a fully catalytic, asymmetric synthesis of 4H-chromenes starting from 2-alkyl-substituted phenols. The aerobic oxidation toward a transient ortho-quinone methide was efficiently catalyzed by a manganese(III) species MnL3 while the ensuing Michael addition of β-dicarbonyl compounds proved to be catalyzed by a chiral manganese phosphate MnL2X*.Entities:
Year: 2017 PMID: 28809505 DOI: 10.1021/acs.orglett.7b02185
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005