Concise and selective: the title one-pot sequence allows formation of the enone functionality and subsequent cross-coupling. The process provides access to highly functionalized cyclic enolones and enaminones from readily accessible β-heteroatom-substituted cyclic ketones.
Mit einer Tandemsequenz (siehe Schema) gelingt in einem einzigen Synthesegang die Einführung einer Enon‐Funktionalität durch Dehydrierung und die anschließende Kreuzkupplung der Zwischenstufe. Der Prozess erzeugt hoch funktionalisierte cyclische Enolone und Enaminone aus einfach zugänglichen heterocyclischen Ketonen.
Palladium-Catalyzed Dehydrogenation/Oxidative Cross-Coupling Sequence of β-Heteroatom-Substituted Ketones. -The title sequence is studied for various heterocyclic systems such as (VII), (X), (XIII) and (XV) and leads to C-3 functionalized systems. Additionally, a dehydrogenation/arylation of the chromanone scaffold (I) or (IV) becomes possible after a slight variation in the conditions to produce C-2 substituted derivatives. -(MOON, Y.; KWON, D.; HONG*, S.; Angew. Chem., Int. Ed. 51 (2012) 45, 11333-11336, http://dx.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.