Preparation of Rearranged Allylic Isocyanates from the Reaction of Allylic Alcohols with 1-Cyano-4-dimethylaminopyridinium Bromide
dc.contributor.author | Baidilov, Daler | |
dc.contributor.author | Makarova, Mariia | |
dc.contributor.author | Rycek, Lukas | |
dc.contributor.author | Hudlicky, Tomas | |
dc.date.accessioned | 2019-01-16T18:44:10Z | |
dc.date.available | 2019-01-16T18:44:10Z | |
dc.date.issued | 2018-10-11 | |
dc.identifier.citation | Synthesis 2018, 50, 4606–4610 | en_US |
dc.identifier.issn | 1437-210X | |
dc.identifier.uri | http://hdl.handle.net/10464/13885 | |
dc.description.abstract | A shorter and less costly alternative to Ichikawa’s [1,3]-transposition protocol for cyanates to isocyanates is described. | en_US |
dc.description.sponsorship | Natural Sciences and Engineering Research Council of Canada (NSERC) (Idea to Innovation and Discovery Grants), Canada Research Chair Program, Canada Foundation for Innovation (CFI), TDC Research, Inc., TDC Research Foundation, the Ontario Partnership for Innovation and Commercialization (OPIC), and The Advanced Biomanufacturing Centre (Brock University). | en_US |
dc.language.iso | en | en_US |
dc.publisher | Thieme | en_US |
dc.subject | sigmatropic rearrangement | en_US |
dc.subject | [1,3]-transposition | en_US |
dc.subject | allylic alcohol | en_US |
dc.subject | methodology | en_US |
dc.subject | total synthesis | en_US |
dc.title | Preparation of Rearranged Allylic Isocyanates from the Reaction of Allylic Alcohols with 1-Cyano-4-dimethylaminopyridinium Bromide | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1055/s-0037-1610659 | |
refterms.dateFOA | 2019-10-11T00:00:00Z |