A Transition Metal-Free Minisci Reaction: Acylation of Isoquinolines, Quinolines, and Quinoxaline


Autoria(s): Siddaraju, Yogesh; Lamani, Manjunath; Prabhu, Kandikere Ramaiah
Data(s)

2014

Resumo

Transition metal-free acylation of isoquinoline, quinoline, and quinoxaline derivatives has been developed employing a cross dehydrogenative coupling (CDC) reaction with aldehydes using substoichiometric amount of TBAB (tetrabutylammonium bromide, 30 mol %) and K2S2O8 as an oxidant. This intermolecular acylation of electron-deficient heteroarenes provides an easy access and a novel acylation method of heterocyclic compounds. The application of this CDC strategy for acylation strategy has been illustrated in synthesizing isoquinoline-derived natural products.

Formato

application/pdf

Identificador

http://eprints.iisc.ernet.in/49218/1/jou_org_che_79-9_3856_2014.pdf

Siddaraju, Yogesh and Lamani, Manjunath and Prabhu, Kandikere Ramaiah (2014) A Transition Metal-Free Minisci Reaction: Acylation of Isoquinolines, Quinolines, and Quinoxaline. In: JOURNAL OF ORGANIC CHEMISTRY, 79 (9). pp. 3856-3865.

Publicador

AMER CHEMICAL SOC

Relação

http://dx.doi.org/10.1021/jo500294z

http://eprints.iisc.ernet.in/49218/

Palavras-Chave #Organic Chemistry
Tipo

Journal Article

PeerReviewed