Next Article in Journal
Acknowledgement to Reviewers of Molbank in 2016
Previous Article in Journal
Open AccessShort Note


Centre of Polymer Systems, University Institute, Tomas Bata University in Zlin, Tř. T. Bati 5678, 760 01, Zlin, Czech Republic
Biological Nanostructures Facility, Molecular Foundry, Lawrence Berkeley National Laboratory1 Cyclotron Rd., Berkeley, CA 94720, USA
Author to whom correspondence should be addressed.
Academic Editor: Norbert Haider
Molbank 2017, 2017(1), M925;
Received: 21 September 2016 / Revised: 26 December 2016 / Accepted: 4 January 2017 / Published: 9 January 2017
(This article belongs to the Section Organic Synthesis)
Ethyl({[acryloyl(furan-2-ylmethyl)amino]acetyl}amino)acetate was synthesized via Ugi four component (4C) reaction at ambient temperature. The protocol employs a reaction between formaldehyde, furfurylamine, acrylic acid, and ethyl 2-isocyanoacetate. The course of the reaction was found to be high yielding, and the resulting glycine ester derivative was well characterized by elemental analysis, FTIR, NMR spectroscopy, and mass spectrometric techniques. View Full-Text
Keywords: FTIR; NMR; peptides; peptoids; Ugi reaction FTIR; NMR; peptides; peptoids; Ugi reaction
MDPI and ACS Style

Ganesh, S.D.; Saha, N.; Zuckermann, R.N.; Sáha, P. Ethyl({[acryloyl(furan-2-ylmethyl)amino]acetyl}amino)acetate. Molbank 2017, 2017, M925.

Show more citation formats Show less citations formats
Note that from the first issue of 2016, MDPI journals use article numbers instead of page numbers. See further details here.

Article Access Map by Country/Region

Back to TopTop