Abstract
The first reported acyl and sulfonylisocyanates were developed and tested in reactions with chiral alcohols to afford diastereomeric carbamates. NMR analysis of these investigates the chemical shift discrimination that would allow these activated isocyanates to be used as diagnostic probes of enantiomeric purity.
Keywords
Publication details
- DOI
- 10.24200/squjs.vol5iss0pp11-23
- Journal
- Sultan Qaboos University Journal for Science, 5, 11
- Publisher
- Sultan Qaboos University
- Open access
- Gold open access
- License
- CC BY 4.0
Cite this article
APA 7
ROOS, G. H. P., & Donovanb, A. R. (2000). Homochiral Acyl Isocyanates as Diagnostic NMR Probes for the Enantiomeric Purity of Chiral Alcohols. Sultan Qaboos University Journal for Science, 5, 11. https://doi.org/10.24200/squjs.vol5iss0pp11-23
MLA 9
ROOS, GREGORY H. P., and Anthony R. Donovanb. "Homochiral Acyl Isocyanates as Diagnostic NMR Probes for the Enantiomeric Purity of Chiral Alcohols." Sultan Qaboos University Journal for Science, vol. 5, 2000, pp. 11. https://doi.org/10.24200/squjs.vol5iss0pp11-23.
Chicago (author–date)
ROOS, GREGORY H. P., and Anthony R. Donovanb. 2000. "Homochiral Acyl Isocyanates as Diagnostic NMR Probes for the Enantiomeric Purity of Chiral Alcohols." Sultan Qaboos University Journal for Science 5: 11. https://doi.org/10.24200/squjs.vol5iss0pp11-23.
Harvard
ROOS, G. H. P. and Donovanb, A. R. (2000) 'Homochiral Acyl Isocyanates as Diagnostic NMR Probes for the Enantiomeric Purity of Chiral Alcohols', Sultan Qaboos University Journal for Science, 5, pp. 11. doi:10.24200/squjs.vol5iss0pp11-23.
Vancouver
ROOS GHP, Donovanb AR. Homochiral Acyl Isocyanates as Diagnostic NMR Probes for the Enantiomeric Purity of Chiral Alcohols. Sultan Qaboos University Journal for Science. 2000;5:11. doi:10.24200/squjs.vol5iss0pp11-23
IEEE
G. H. P. ROOS, and A. R. Donovanb, "Homochiral Acyl Isocyanates as Diagnostic NMR Probes for the Enantiomeric Purity of Chiral Alcohols," Sultan Qaboos University Journal for Science, vol. 5, pp. 11, 2000, doi: 10.24200/squjs.vol5iss0pp11-23.