Abstract
13C NMR spectroscopy was used for the unequivocal analysis of the mixture of products of RuCl2[P(C6H5)3]3‐catalysed transfer deuteriation of benzylideneacetophenone by (a) DCOONa/H2O, (b) HCOONa/D2O and (c) DCOONa/D2O. Signal assignments in the 13C spectra were obtained mainly from the deuterium‐induced 13C isotope shifts. The geminal 13C2H shift of the β‐carbon of deuteriated 1,3‐diphenylpropan‐1‐one is almost twice that for the α‐carbon.
| Original language | English |
|---|---|
| Pages (from-to) | 565-568 |
| Number of pages | 4 |
| Journal | Organic Magnetic Resonance |
| Volume | 22 |
| Issue number | 9 |
| DOIs | |
| State | Published - Sep 1984 |
Fingerprint
Dive into the research topics of 'Use of 13C isotope shifts for assignment of deuterium labelling sites in 1,3‐diphenylpropan‐1‐one'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver