Photocatalytic Dehydrogenative Lactonization of 2-Arylbenzoic Acids


Autoria(s): Ramírez, Nieves P.; Bosque, Irene; Gonzalez-Gomez, Jose C.
Contribuinte(s)

Universidad de Alicante. Departamento de Química Orgánica

Universidad de Alicante. Instituto Universitario de Síntesis Orgánica

Catálisis Estereoselectiva en Síntesis Orgánica (CESO)

Síntesis Asimétrica (SINTAS)

Data(s)

08/02/2016

08/02/2016

31/08/2015

Resumo

A metal-free dehydrogenative lactonization of 2-arylbenzoic acids at room temperature was developed. This work illustrates the first application of visible-light photoredox catalysis in the preparation of benzo-3,4-coumarins, an important structural motif in bioactive molecules. The combination of photocatalyst [Acr+-Mes] with (NH4)2S2O8 as a terminal oxidant provides an economical and environmentally benign entry to different substituted benzocoumarins. Preliminary mechanistic studies suggest that this reaction most likely occurs through a homolytic aromatic substitution pathway.

We thank the Spanish Ministerio de Ciencia e Innovación (CTQ2011-24165) for financial support. I.B. acknowledges the Generalitat Valenciana for a postdoctoral fellowship (ACIF/2011/159).

Identificador

Organic Letters. 2015, 17(18): 4550-4553. doi:10.1021/acs.orglett.5b02269

1523-7060 (Print)

1523-7052 (Online)

http://hdl.handle.net/10045/52884

10.1021/acs.orglett.5b02269

Idioma(s)

eng

Publicador

American Chemical Society

Relação

http://dx.doi.org/10.1021/acs.orglett.5b02269

Direitos

© 2015 American Chemical Society

info:eu-repo/semantics/openAccess

Palavras-Chave #Photocatalytic #Dehydrogenative #Lactonization #2-arylbenzoic acids #Química Orgánica
Tipo

info:eu-repo/semantics/article