| Literature DB >> 22555554 |
Steven Giboulot1, Frédéric Liron, Guillaume Prestat, Benoit Wahl, Mathieu Sauthier, Yves Castanet, André Mortreux, Giovanni Poli.
Abstract
In the presence of an allyl alcohol, α-chloroacetophenones undergo an allyloxycarbonylation reaction followed by in situ decarboxylative allylation to selectively afford the corresponding monoallylated ketones via a Pd-catalyzed domino sequence. The scope of the reaction was extended to substituted α-chloroacetophenones as well as various allyl alcohols.Entities:
Year: 2012 PMID: 22555554 DOI: 10.1039/c2cc32391e
Source DB: PubMed Journal: Chem Commun (Camb) ISSN: 1359-7345 Impact factor: 6.222