Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10259/7412
Título
Asymmetric Gold(I)‐Catalyzed Tandem Hydroarylation–Nazarov Cyclization: Enantioselective Access to Cyclopentenones
Publicado en
Angewandte Chemie International Edition. 2022, V. 61, n. 35, e202207406
Editorial
Wiley
Fecha de publicación
2022
ISSN
1433-7851
DOI
10.1002/anie.202207406
Abstract
The asymmetric synthesis of cyclopentachromenones from gold-catalyzed reaction of readily available skipped alkenynones is described. This cascade
reaction involves an initial anti-Michael hydroarylation
of the ynone moiety to form a gold-functionalized
dialkenylketone intermediate, followed by a Nazarov
cyclization that proceeds in an unprecedented enantioselective manner. Excellent enantiomeric ratios and chemical yields are obtained under mild reaction conditions.
Palabras clave
Asynmetric Catalysis
Cyclopentenones
Gold
Hydroarylation
Nazarov Cyclization
Materia
Química orgánica
Chemistry, Organic
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