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The rapid generation of isothiocyanates in flow
- Source :
- Beilstein journal of organic chemistry, 2013, Vol.9, pp.1613-1619 [Peer Reviewed Journal], Beilstein Journal of Organic Chemistry, Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 1613-1619 (2013)
- Publication Year :
- 2013
- Publisher :
- Beilstein Institut, 2013.
-
Abstract
- Isothiocyanates are versatile starting materials for a wide range of chemical reactions. However, their high nucleophilic susceptibility means they are best prepared and used immediately. We report here on a flow platform for the fast and efficient formation of isothiocyanates by the direct conversion of easily prepared chloroximes. To expedite this chemistry a flow insert cartridge containing two immobilised reagents is used to affect the chemical transformation which typically eliminates the requirements for any conventional work-up or purification of the reaction stream.
- Subjects :
- Chemical transformation
Nitrile oxide
flow chemistry
flow synthesis
Chemical reaction
Full Research Paper
lcsh:QD241-441
chemistry.chemical_compound
Cartridge
immobilised reagents
Isothiocyanate
lcsh:Organic chemistry
Nucleophile
Organic chemistry
lcsh:Science
Flow chemistry
Chemistry
Organic Chemistry
Chloroxime
chloroxime
Dipolar cycloaddition
dipolar cycloaddition
nitrile oxide
Reagent
lcsh:Q
Immobilised reagents
isothiocyanate
Flow synthesis
Subjects
Details
- Database :
- OpenAIRE
- Journal :
- Beilstein journal of organic chemistry, 2013, Vol.9, pp.1613-1619 [Peer Reviewed Journal], Beilstein Journal of Organic Chemistry, Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 1613-1619 (2013)
- Accession number :
- edsair.doi.dedup.....ec1d1cbedf3f85b254e1766dc1c87b8b