Abstract
Hydroboration of 3- and 4-methyl- and 3- and 4-t-butylmethylenecyelohexanes yielded, after oxidation, predominantly the axial-equatorial disubstituted cyclohexanes. Similar results were obtained when dichloroborane was used as the hydroborating agent. Dicyclohexylborane gave equal amounts of axial and equatorial products.
| Original language | English |
|---|---|
| Pages (from-to) | 2654-2656 |
| Number of pages | 3 |
| Journal | Journal of Organic Chemistry |
| Volume | 35 |
| Issue number | 8 |
| DOIs | |
| State | Published - 1 Aug 1970 |