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A transition-metal-free fast track to flavones and 3-arylcoumarins

Citation

Golshani, M and Khoobi, M and Jalalimanesh, N and Jafarpour, F and Ariafard, A, A transition-metal-free fast track to flavones and 3-arylcoumarins, Chemical Communications, 53, (77) pp. 10676-10679. ISSN 1359-7345 (2017) [Refereed Article]

Copyright Statement

Copyright 2017 The Royal Society of Chemistry

DOI: doi:10.1039/c7cc02107k

Abstract

A highly regioselective and transition-metal free one-pot arylation of chromenones with arylboronic acids has been achieved employing K2S2O8. The procedure consists of a sequence of some reactions including an arylation/decarboxylation cascade and proceeds well in aqueous media to afford biologically interesting flavones and 3-arylcoumarins. This method exhibited excellent selectivity and functional group tolerance under mild conditions. The reaction also showed perfect efficacy for the preparation of styryl coumarins.

Item Details

Item Type:Refereed Article
Keywords:transition-metal-free, catalysis, DFT calculation, arylboronic acid, decarboxylation, redox process
Research Division:Chemical Sciences
Research Group:Physical Chemistry (incl. Structural)
Research Field:Catalysis and Mechanisms of Reactions
Objective Division:Expanding Knowledge
Objective Group:Expanding Knowledge
Objective Field:Expanding Knowledge in the Chemical Sciences
Author:Ariafard, A (Associate Professor Alireza Ariafard)
ID Code:123466
Year Published:2017
Web of Science® Times Cited:1
Deposited By:Chemistry
Deposited On:2018-01-09
Last Modified:2018-03-27
Downloads:0

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