A Transition Metal-Free Minisci Reaction: Acylation of Isoquinolines, Quinolines, and Quinoxaline
Data(s) |
2014
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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 |