110220-77-4Relevant academic research and scientific papers
Regioselective opening of chalcone epoxides with nitrogen heterocycles using indium(III) chloride as an efficient catalyst
Konduru, Naveen Kumar,Ahmed, Naseem
supporting information, p. 2008 - 2018 (2013/06/27)
Indium(III) chloride catalyzes regioselective ring opening of chalcone epoxides with nitrogen heterocycles such as indole, 2-methyl indole, and pyrrole under mild conditions at room temperature to afford 1,3-diaryl-2-hydroxy-3-(1H- 3-indolyl/2-pyrrolyl)propan-1-ones in good yields (60-88%) within 20-50 min. Supplemental materials are available for this article. Go to the publisher's online edition of Synthetic Communications to view the free supplemental file.
Mild and convenient epoxidation of α,β-unsaturated ketones by amberlyst A-26 supported hydroperoxide
Lakouraj,Movassagh,Bahrami
, p. 1237 - 1242 (2007/10/03)
The epoxidation of α,β-unsaturated ketones to the corresponding epoxy ketones, using amberlyst A-26 supported hydroperoxide, which is prepared in situ from (35%) hydrogen peroxide and amberlyst A-26(OH-), is described. Reactions were carried out at room temperature and the corresponding epoxides were isolated in excellent yields.
