Abstract
The stereoselective hydrogenation of alkynes to alkenes is an extremely useful transformation in synthetic chemistry. Despite numerous reports for the synthesis of Zalkenes, the hydrogenation of alkynes to give E-alkenes is still not well resolved. In particular, selective preparation of both Z- and E-alkenes by the same catalytic hydrogenation system using molecular H2 has rarely been reported. In this paper, a novel strategy of using simple alkenes as promoters for the HB(C6F5)2-catalyzed metal-free hydrogenation of alkynes was adopted. Significantly, both Z - and E-alkenes can be furnished by hydrogenation with molecular H2 in high yields with excellent stereoselectivities. Further experimental and theoretical mechanistic studies suggest that interactions between H and F atoms of the alkene promoter, borane intermediate, and H2 play an essential role in promoting the hydrogenolysis reaction.
| Original language | English |
|---|---|
| Pages (from-to) | 3495-3501 |
| Number of pages | 7 |
| Journal | Chemistry - A European Journal |
| Volume | 21 |
| Issue number | 8 |
| DOIs | |
| State | Published - 16 Feb 2015 |
| Externally published | Yes |
Keywords
- Alkene
- Alkyne
- Hydrogenation
- Metal-free catalysis
- Stereoselectivity