A study of selectivity in the reactions of unsymmetrical trialkylboron compounds
The reaction of disiamylborane with enol acetates derived from an aldehyde bearing two α-hydrogen atoms involves a slow anti-Markownikoff hydroboration followed by rapid elimination and re-hydroboration reactions. Selectivity between reaction of the cis and trans isomers is far smaller than for the...
Saved in:
| Main Author: | |
|---|---|
| Format: | Default Thesis |
| Published: |
1967
|
| Subjects: | |
| Online Access: | https://hdl.handle.net/2134/36020 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|