Files in this item
Conformational preferences of Ac-Gly-NHMe in solution
Item metadata
dc.contributor.author | Cormanich, Rodrigo Antonio | |
dc.contributor.author | Rittner, Roberto | |
dc.contributor.author | Buehl, Michael | |
dc.date.accessioned | 2016-01-13T00:12:08Z | |
dc.date.available | 2016-01-13T00:12:08Z | |
dc.date.issued | 2015 | |
dc.identifier.citation | Cormanich , R A , Rittner , R & Buehl , M 2015 , ' Conformational preferences of Ac-Gly-NHMe in solution ' , RSC Advances , vol. 5 , no. 16 , pp. 13052-13060 . https://doi.org/10.1039/C4RA16472E | en |
dc.identifier.issn | 2046-2069 | |
dc.identifier.other | PURE: 161860563 | |
dc.identifier.other | PURE UUID: 0cb56d5e-a2a4-4cf4-ac4a-0f1b58e06477 | |
dc.identifier.other | WOS: 000348987700072 | |
dc.identifier.other | Scopus: 84961365703 | |
dc.identifier.other | ORCID: /0000-0002-1095-7143/work/48131806 | |
dc.identifier.uri | https://hdl.handle.net/10023/8010 | |
dc.description | The authors thank a Grant # 2012/03933-5, São Paulo Research Foundation (FAPESP) for providing financial support for this research and a scholarship to RAC #2011/01170-1 (FAPESP). CNPq is also acknowledged, such as for fellowships (to RR) and a studentship (to RAC). | en |
dc.description.abstract | The conformational behaviour of Ac-Gly-NHMe in nonpolar, polar and polar protic solutions was systematically studied in this work by theoretical calculations and experimental infrared and 1H NMR spectroscopies. Ac-Gly-NHMe prefers a gauche conformer with a strong seven-membered intramolecular hydrogen bond for the isolated compound and in nonpolar solvents, but such preference changes in polar and polar protic solvents. Elucidation of Ac-Gly-NHMe preferences was also supported by studying the conformers of its CF3-C(O)-Gly-NHMe and Ac-Gly-N(Me)2 derivatives in solution. | |
dc.language.iso | eng | |
dc.relation.ispartof | RSC Advances | en |
dc.rights | © Royal Society of Chemistry 2015. No further copies may be made or distributed. This work is made available online in accordance with the publisher’s policies. This is the author created, accepted version manuscript following peer review and may differ slightly from the final published version. The final published version of this work is available at http://dx.doi.org/10.1039/C4RA16472E | en |
dc.subject | QD Chemistry | en |
dc.subject | NDAS | en |
dc.subject.lcc | QD | en |
dc.title | Conformational preferences of Ac-Gly-NHMe in solution | en |
dc.type | Journal article | en |
dc.description.version | Postprint | en |
dc.contributor.institution | University of St Andrews. School of Chemistry | en |
dc.contributor.institution | University of St Andrews. EaSTCHEM | en |
dc.identifier.doi | https://doi.org/10.1039/C4RA16472E | |
dc.description.status | Peer reviewed | en |
dc.date.embargoedUntil | 2016-01-13 |
This item appears in the following Collection(s)
Items in the St Andrews Research Repository are protected by copyright, with all rights reserved, unless otherwise indicated.