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Octahydro-1H,5H,7H-dipyrrolo[1,2-c:1',2'-f][1,3,6]oxadiazocine-5-thione
Item metadata
| dc.contributor.author | Aitken, R. Alan | |
| dc.contributor.author | Ali, Karamat | |
| dc.date.accessioned | 2018-04-30T10:30:08Z | |
| dc.date.available | 2018-04-30T10:30:08Z | |
| dc.date.issued | 2018-04-27 | |
| dc.identifier.citation | Aitken , R A & Ali , K 2018 , ' Octahydro-1 H ,5 H ,7 H -dipyrrolo[1,2-c:1',2'- f ][1,3,6]oxadiazocine-5-thione ' , Molbank , vol. 2018 , M993 . https://doi.org/10.3390/M993 | en |
| dc.identifier.issn | 1422-8599 | |
| dc.identifier.other | PURE: 252933976 | |
| dc.identifier.other | PURE UUID: 7fcb0eb5-fae2-4909-b1a2-9e275471eaa4 | |
| dc.identifier.other | Scopus: 85047433112 | |
| dc.identifier.other | ORCID: /0000-0001-6959-5311/work/44130494 | |
| dc.identifier.other | WOS: 000436155900006 | |
| dc.identifier.uri | https://hdl.handle.net/10023/13261 | |
| dc.description.abstract | A minor byproduct in the reaction of (S)-prolinol with thiophosgene in the presence of triethylamine is identified as a novel tricyclic dipyrrolidino-1,3,6-oxadiazocane-2-thione, the first example of such a ring system, and a representative of the uncommon but useful 1,3,6-oxadiazocanes. A mechanism is proposed for its formation. | |
| dc.format.extent | 5 | |
| dc.language.iso | eng | |
| dc.relation.ispartof | Molbank | en |
| dc.rights | © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). | en |
| dc.subject | 1,3,6-oxadiazocane | en |
| dc.subject | 1,3,6-oxadiazocine-2-thione | en |
| dc.subject | NMR spectra | en |
| dc.subject | QD Chemistry | en |
| dc.subject | NDAS | en |
| dc.subject.lcc | QD | en |
| dc.title | Octahydro-1H,5H,7H-dipyrrolo[1,2-c:1',2'-f][1,3,6]oxadiazocine-5-thione | en |
| dc.type | Journal article | en |
| dc.description.version | Publisher PDF | 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/10.3390/M993 | |
| dc.description.status | Peer reviewed | en |
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