New Simple Synthesis of N-Substituted 1,3-Oxazinan-2-ones

Trifunovic S, Dimitrijevic D, Vasic G, Radulovic N, Vukicevic M, Heinemann FW, Vukicevic RD (2010)


Publication Status: Published

Publication Type: Journal article

Publication year: 2010

Journal

Publisher: GEORG THIEME VERLAG KG

Pages Range: 943-946

Journal Issue: 6

DOI: 10.1055/s-0029-1218642

Abstract

An efficient and simple synthesis of N-substituted 1,3-oxazinan-2-ones was developed that involves a three-component, one-pot reaction of readily available tetraethylammonium bicarbonate, 1,3-dibromopropane, and a primary amine in methanol at room temperature. L-Alanine can be used as the amino component to give the chiral product (2S)-2-(2-oxo-1,3-oxazinan-3-yl)propanoic acid.

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APA:

Trifunovic, S., Dimitrijevic, D., Vasic, G., Radulovic, N., Vukicevic, M., Heinemann, F.W., & Vukicevic, R.D. (2010). New Simple Synthesis of N-Substituted 1,3-Oxazinan-2-ones. Synthesis-Stuttgart, 6, 943-946. https://dx.doi.org/10.1055/s-0029-1218642

MLA:

Trifunovic, Srecko, et al. "New Simple Synthesis of N-Substituted 1,3-Oxazinan-2-ones." Synthesis-Stuttgart 6 (2010): 943-946.

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