Issue 94, 2016

Tandem additions of 3,4-dihydroisoquinolines to γ-hydroxy-α,β-unsaturated ketones: a green and new access to oxazolo[2,3-a]tetrahydroisoquinolines

Abstract

Addition reaction of 3,4-dihydroisoquinolines with γ-hydroxy-α,β-unsaturated ketones furnished a variety of diastereomerically pure oxazolo[2,3-a]tetrahydro-isoquinolines, which could be purified by either recrystallization or solvent evaporation. The reaction proceeded smoothly under “green” conditions without an additive and catalyst, giving the target molecules in good to excellent yields.

Graphical abstract: Tandem additions of 3,4-dihydroisoquinolines to γ-hydroxy-α,β-unsaturated ketones: a green and new access to oxazolo[2,3-a]tetrahydroisoquinolines

Supplementary files

Article information

Article type
Communication
Submitted
17 Aug 2016
Accepted
20 Sep 2016
First published
21 Sep 2016

RSC Adv., 2016,6, 91870-91874

Tandem additions of 3,4-dihydroisoquinolines to γ-hydroxy-α,β-unsaturated ketones: a green and new access to oxazolo[2,3-a]tetrahydroisoquinolines

S. Huang, Y. Shih, W. Huang, D. Li and T. Yang, RSC Adv., 2016, 6, 91870 DOI: 10.1039/C6RA20708A

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