dc.contributor.author | Wood, ME | |
dc.contributor.author | Annis, VM | |
dc.contributor.author | Jones, Clifford D. | |
dc.date.accessioned | 2013-06-04T10:22:24Z | |
dc.date.issued | 2008-11-21 | |
dc.description.abstract | Crystalline samples of three N-aroyl-1,2,4-dithiazolidine-3,5-diones have been prepared as the first examples of a novel class of compound that displays the reactivity of an acyl isocyanate when treated with nucleophiles. | en_GB |
dc.identifier.citation | Organic and Biomolecular Chemistry, 2008, Vol. 6, Issue 22, pp. 4099 - 4101 | en_GB |
dc.identifier.doi | 10.1039/b814677b | |
dc.identifier.uri | http://hdl.handle.net/10871/9828 | |
dc.language.iso | en | en_GB |
dc.publisher | Royal Society of Chemistry | en_GB |
dc.relation.url | http://www.ncbi.nlm.nih.gov/pubmed/18972038 | en_GB |
dc.rights | Copyright © 2008 Royal Society of Chemistry | |
dc.subject | Imides | en_GB |
dc.subject | Isocyanates | en_GB |
dc.subject | Thiazolidines | en_GB |
dc.title | Unusual reactivity of N-acyl imides: N-aroyl-1,2,4-dithiazolidine-3,5-diones as acyl isocyanate equivalents. | en_GB |
dc.type | Article | en_GB |
dc.date.available | 2013-06-04T10:22:24Z | |
exeter.place-of-publication | England | |
dc.identifier.journal | Organic and Biomolecular Chemistry | en_GB |