Four novel stereoisomers of 7-(1-phenylethyl)-2-oxa-7-azabicyclo[3.2.0]heptan-6-one were prepared under high pressure from [2 ] 2] cycloaddition of the pure enantiomers of 1-phenylethyl isocyanate and 2,3dihydrofuran. Their conformational preferences in solution and the absolute conÐgurations of the
The use of chiral shift reagents in an NMR study of 2,2′,6,6′-tetrasubstituted biphenyls
✍ Scribed by E. Diaz; E. Rojas-Dávila; A. Guzmán; P. Joseph-Nathan
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- English
- Weight
- 429 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The determination of the enantiomeric composition of 2,2′,6′6′‐tetrasubstituted biphenyls using ^1^H NMR spectroscopy, in combination with chiral lanthanide shift reagents, has been studied. In general, the S compounds give largeer induced shifts than the correspondind R isomers when d‐camphor derived shift reagents are used.
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