Abstract
Copper catalyzed enantioselective [4 + 2] annulations of D-A cyclobutanes and aldehydes have been developed. In the presence of a side arm modified chiral bisoxazoline (SaBOX) ligand, the [4 + 2] annulations proceeded smoothly with a broad substrate scope. 22 examples were studied, leading to the corresponding products with various functional groups in 41%–99% yields with >99/1 dr and 90%–96% ee. The resulting product with two ester groups was mono-reduced, giving the corresponding product in excellent diastereoselectivity without loss of the enantiopurity.
| Original language | English |
|---|---|
| Pages (from-to) | 47-50 |
| Number of pages | 4 |
| Journal | Chinese Journal of Chemistry |
| Volume | 36 |
| Issue number | 1 |
| DOIs | |
| State | Published - 1 Jan 2018 |
| Externally published | Yes |
Keywords
- [4 + 2] annulation
- bisoxazoline
- copper
- cyclobutane
- enantioselective