Research output: Contribution to Journal/Magazine › Journal article › peer-review
| <mark>Journal publication date</mark> | 15/02/2018 |
|---|---|
| <mark>Journal</mark> | Synthesis (Germany) |
| Issue number | 4 |
| Volume | 50 |
| Number of pages | 6 |
| Pages (from-to) | 803-808 |
| Publication Status | Published |
| <mark>Original language</mark> | English |
Simple, commercially available borane adducts, H 3 B·THF and H 3 B·SMe 2, have been used to catalyse the hydroboration of alkynes and alkenes with pinacolborane to give the alkenyl and alkyl boronic esters, respectively. Alkynes and terminal alkenes underwent highly regioselective hydroboration to give the linear boronic ester products. Good functional group tolerance was observed for substrates bearing ester, amine, ether and halide substituents. This catalytic process shows comparable reactivity to transition-metal-catalysed hydroboration protocols.