| Download | - View final version: Alkanes with multiple asymmetric centers: synthesis, identification, and ¹³C nuclear magnetic resonance spectra (PDF, 562 KiB)
|
|---|
| DOI | Resolve DOI: https://doi.org/10.1139/v79-061 |
|---|
| Author | Search for: Lachance, Pierre1; Search for: Brownstein, S.1; Search for: Eastham, Arthur M.1 |
|---|
| Affiliation | - National Research Council of Canada
|
|---|
| Format | Text, Article |
|---|
| Abstract | The identification of aliphatic hydrocarbons containing multiple asymmetric centers can be difficult because of the complexity of the nmr spectra and because in capillary chromatography the diastereomers may be resolved to varying degrees. We suggest that the most effective method for identifying such hydrocarbons is through the pattern of retention times developed by the mixture of diastereomers on a suitable capillary glc column.This paper presents the results of some studies of a series of alkanes having the general form C₂H₅—(CH—CH₃)n—R, where n = 1 to 4, and includes the syntheses and ¹³C nmr spectra of the compounds. |
|---|
| Publication date | 1979-02-15 |
|---|
| Publisher | Canadian Science Publishing |
|---|
| In | |
|---|
| Language | English |
|---|
| Peer reviewed | Yes |
|---|
| Identifier | NRCC-17064 |
|---|
| Export citation | Export as RIS |
|---|
| Report a correction | Report a correction (opens in a new tab) |
|---|
| Record identifier | e664a9d2-d2c2-474f-825e-ebcf4ceea960 |
|---|
| Record created | 2023-09-05 |
|---|
| Record modified | 2023-09-05 |
|---|
