Ethyl({[acryloyl(furan-2-ylmethyl)amino]acetyl}amino)acetate

Shimoga Dinesh, Ganesh; Saha, Nabanita; Zuckermann, Ronald N.; Sáha, Petr

dc.title	Ethyl({[acryloyl(furan-2-ylmethyl)amino]acetyl}amino)acetate	en
dc.contributor.author	Shimoga Dinesh, Ganesh
dc.contributor.author	Saha, Nabanita
dc.contributor.author	Zuckermann, Ronald N.
dc.contributor.author	Sáha, Petr
dc.relation.ispartof	MolBank
dc.identifier.issn	1422-8599 Scopus Sources, Sherpa/RoMEO, JCR
dc.date.issued	2017
utb.relation.volume	2017
utb.relation.issue	1
dc.type	article
dc.language.iso	en
dc.publisher	MDPI AG
dc.identifier.doi	10.3390/M925
dc.relation.uri	http://www.mdpi.com/1422-8599/2017/1/M925
dc.subject	FTIR	en
dc.subject	NMR	en
dc.subject	peptides	en
dc.subject	peptoids	en
dc.subject	Ugi reaction	en
dc.description.abstract	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. © 2017 by the authors; licensee MDPI, Basel, Switzerland.	en
utb.faculty	University Institute
dc.identifier.uri	http://hdl.handle.net/10563/1006899
utb.identifier.obdid	43877202
utb.identifier.scopus	2-s2.0-85009730038
utb.identifier.wok	000418113500004
utb.source	j-scopus
dc.date.accessioned	2017-06-27T08:13:10Z
dc.date.available	2017-06-27T08:13:10Z
dc.description.sponsorship	DE-AC02-05CH11231, DOE, U.S. Department of Energy; MŠMT, Ministerstvo Školství, Mládeže a Tělovýchovy
dc.description.sponsorship	MSMT CR-USA Kontakt II [LH14050]; Molecular Foundry, Office of Science, Office of Basic Energy Sciences, of the U.S. Department of Energy [DE-AC02-05CH11231]; Ministry of Education, Youth and Sports of the Czech Republic - NPU Program I [LO1504]
dc.rights	Attribution 4.0 International
dc.rights.uri	https://creativecommons.org/licenses/by/4.0/
dc.rights.access	openAccess
utb.ou	Centre of Polymer Systems
utb.contributor.internalauthor	Shimoga Dinesh, Ganesh
utb.contributor.internalauthor	Saha, Nabanita
utb.contributor.internalauthor	Sáha, Petr
utb.fulltext.affiliation	Shimoga D. Ganesh 1 , Nabanita Saha 1, , Ronald N. Zuckermann 2 and Petr Sáha 1 1 Centre of Polymer Systems, University Institute, Tomas Bata University in Zlin, Tř. T. Bati 5678, 760 01, Zlin, Czech Republic; icganeshin@gmail.com (S.D.G.); saha@utb.cz (P.S.) 2 Biological Nanostructures Facility, Molecular Foundry, Lawrence Berkeley National Laboratory1 Cyclotron Rd., Berkeley, CA 94720, USA; rnzuckermann@lbl.gov Correspondence: nabanita@ft.utb.cz; Tel.: +420-576-038-156
utb.fulltext.dates	Received: 21 September 2016 Accepted: 4 January 2017 Published: 9 January 2017
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utb.fulltext.sponsorship	The work is supported by MŠMT CR-USA Kontakt II (LH14050) and the Molecular Foundry, Office of Science, Office of Basic Energy Sciences, of the U.S. Department of Energy under Contract No. DE-AC02-05CH11231. This research is also supported in part by a grant from the Ministry of Education, Youth and Sports of the Czech Republic - NPU Program I (LO1504). We also acknowledge Pavel Kucharczyk, Centre of Polymer Systems, University Institute, Tomas Bata University in Zlin, Tř. T. Bati 5678, 760 01, Zlin, Czech Republic, for LCMS measurement.
utb.wos.affiliation	[Ganesh, Shimoga D.; Saha, Nabanita; Saha, Petr] Tomas Bata Univ Zlin, Univ Inst, Ctr Polymer Syst, Tr T Bati 5678, Zlin 76001, Czech Republic; [Zuckermann, Ronald N.] Lawrence Berkeley Natl Lab, Biol Nanostruct Facil Mol Foundry, 1 Cyclotron Rd, Berkeley, CA 94720 USA
utb.fulltext.projects	LH14050
utb.fulltext.projects	DE-AC02-05CH11231
utb.fulltext.projects	LO1504