| dc.contributor.author | Bakka, Thomas Aleksander | |
| dc.contributor.author | Gautun, Odd Reidar | |
| dc.date.accessioned | 2018-04-12T06:17:05Z | |
| dc.date.available | 2018-04-12T06:17:05Z | |
| dc.date.created | 2017-01-09T09:59:19Z | |
| dc.date.issued | 2017 | |
| dc.identifier.citation | Synthetic Communications. 2017, 47 (2), 169-172. | nb_NO |
| dc.identifier.issn | 0039-7911 | |
| dc.identifier.uri | http://hdl.handle.net/11250/2493734 | |
| dc.description.abstract | Improved reaction conditions for the electrophile reaction between a free aliphatic amine and 1H-pyrazole carboxamidine have been discovered. The surfactant-like guanidine salts, which are often hard to work with, were obtained in decent yield with short reaction times, minimal workup, and high level of purity. | nb_NO |
| dc.language.iso | eng | nb_NO |
| dc.publisher | Taylor & Francis | nb_NO |
| dc.title | Simple generalized reaction conditions for the conversion of primary aliphatic amines to surfactant-like guanidine salts with 1H-pyrazole carboxamidine hydrochloride | nb_NO |
| dc.type | Journal article | nb_NO |
| dc.description.version | submittedVersion | nb_NO |
| dc.source.pagenumber | 169-172 | nb_NO |
| dc.source.volume | 47 | nb_NO |
| dc.source.journal | Synthetic Communications | nb_NO |
| dc.source.issue | 2 | nb_NO |
| dc.identifier.doi | 10.1080/00397911.2016.1257724 | |
| dc.identifier.cristin | 1423021 | |
| dc.relation.project | Norges forskningsråd: 224790 | nb_NO |
| dc.description.localcode | This is an [Original Manuscript] of an article published by Taylor & Francis in [Synthetic Communications] on [11 Nov 2016], available at https://www.tandfonline.com/doi/full/10.1080/00397911.2016.1257724 | nb_NO |
| cristin.unitcode | 194,66,25,0 | |
| cristin.unitname | Institutt for kjemi | |
| cristin.ispublished | true | |
| cristin.fulltext | preprint | |
| cristin.qualitycode | 1 | |
