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dc.contributor.authorBaidilov, Daler
dc.contributor.authorMakarova, Mariia
dc.contributor.authorRycek, Lukas
dc.contributor.authorHudlicky, Tomas
dc.date.accessioned2019-01-16T18:44:10Z
dc.date.available2019-01-16T18:44:10Z
dc.date.issued2018-10-11
dc.identifier.citationSynthesis 2018, 50, 4606–4610en_US
dc.identifier.issn1437-210X
dc.identifier.urihttp://hdl.handle.net/10464/13885
dc.description.abstractA shorter and less costly alternative to Ichikawa’s [1,3]-transposition protocol for cyanates to isocyanates is described.en_US
dc.description.sponsorshipNatural 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.isoenen_US
dc.publisherThiemeen_US
dc.subjectsigmatropic rearrangementen_US
dc.subject[1,3]-transpositionen_US
dc.subjectallylic alcoholen_US
dc.subjectmethodologyen_US
dc.subjecttotal synthesisen_US
dc.titlePreparation of Rearranged Allylic Isocyanates from the Reaction of Allylic Alcohols with 1-Cyano-4-dimethylaminopyridinium Bromideen_US
dc.typeArticleen_US
dc.identifier.doi10.1055/s-0037-1610659


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