Correction. Configuration and Conformation of cis - and trans- 3,5-Dimethylvalerlactones.
β Scribed by Carroll, Frank I.; Mitchell, Gordon N.; Blackwell, Joseph T.; Sobti, Asha.; Meck, Ronald.
- Book ID
- 126477176
- Publisher
- American Chemical Society
- Year
- 1976
- Tongue
- English
- Weight
- 151 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0022-3263
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The configuration and conformation of some diastereomeric 4-hydroxy-cis-and -h.uns-l-oxadecalins were inferred by 'H and '3C NMR spectroscopy. The results obtained indicate that the cis-fused compounds are conformationally homogeneous, having the oxygen atom attached to the cyclohexyl ring in the ax
The con6gurations and conformations of cis-and tram-N-methyl-and -N-benzyl-4,5-and -5,6tetramethylenetetrahydm-l,3-o~es were determined by 'H and -C NMR spectroscopy. The cis isomers are conformationally homogeneous, having the hetero atom attached to the cydohexyl ring, in the axial and equatorial