The relative configuration of a methylated undecanehexaol, a fragment of amycin B, with five chirality centers was determined by a complete 1 H and 13 C signal assignment and interpretation of its acetonide derivatives.
13C NMR of coumarins. II—Khellactones: Spectroscopic criteria to establish the relative configuration of the dihydropyran ring
✍ Scribed by F. A. Macías; G. M. Massanet; F. Rodríguez-Luis; J. Salvá; F. R. Fronczek
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- English
- Weight
- 365 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
The "C NMR data of several khellactone derivatives are reported. 'H NMR-based stereochemical criteria are evaluated, and a new criterion based on "C NMR is proposed to establish the relative configuration at C-3' and (2-4' using A6C-3' between trans and cis isomers and AGgem(Me), values. The structure of bans-4'methylkhellactone was determined by x-ray analysis.
📜 SIMILAR VOLUMES
An assignment of relative configurations has been achieved for the diastereomeric racernates(lR2R,lS2S) and (1R2S, 1S2R) of 3,3-dimethyl-l,2-diphenylbuta~-l-ol through the comparative analysis of the respective chemical shifts induced by Eu(fod), in the 'H and '"C NMR spectra, and the corresponding