| Literature DB >> 27487331 |
Igor Iriarte1, Silvia Vera1, Eider Badiola1, Antonia Mielgo1, Mikel Oiarbide2, Jesús M García3, José M Odriozola3, Claudio Palomo4.
Abstract
An efficient, highly diastereo- and enantioselective assembly of acyclic carbonyl fragments possessing nonadjacent all-carbon tertiary/quaternary stereoarrays is reported based on a Brønsted base catalyzed Michael addition/α-protonation sequence involving α-cyanoacetates and 2,4-dimethyl-4-hydroxypenten-3-one as novel methacrylate equivalent.Entities:
Keywords: Brønsted bases; Michael reactions; asymmetric organocatalysis; quaternary stereocenters; stereoselective protonation
Year: 2016 PMID: 27487331 DOI: 10.1002/chem.201603082
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236