| Literature DB >> 33320681 |
Ádám Márk Pálvölgyi1, Jakob Smith1, Michael Schnürch1, Katharina Bica-Schröder1.
Abstract
We report a straightforward and efficient Pd/enamine catalytic procedure for the direct asymmetric α-allylation of branched aldehydes. The use of simple chiral amines and easily prepared achiral or racemic phosphoric acids, together with a suitable Pd-source resulted in a highly active and enantioselective catalyst system for the allylation of various α-branched aldehydes with different allylic alcohols. The reported procedure could provide an easy access to both product antipodes. Furthermore, two possible orthogonal derivatizations of the enantioenriched aldehydes were performed without any decrease in enantioselectivity.Entities:
Year: 2020 PMID: 33320681 DOI: 10.1021/acs.joc.0c02385
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354