Abstract
We reported herein a practical approach to acyclic tertiary α-hydroxy carbonyl compounds in only two chemical steps from alkynes with excellent diastereoselectivity through the oxidation of stereodefined polysubstituted silyl ketone aminals. The products could be smoothly converted to synthetically useful enantiomerically enriched 1,2-diol derivatives.
| Original language | English |
|---|---|
| Pages (from-to) | 614-618 |
| Number of pages | 5 |
| Journal | European Journal of Organic Chemistry |
| Volume | 2018 |
| Issue number | 5 |
| DOIs | |
| State | Published - 7 Feb 2018 |
Keywords
- -Hydroxy carbonyls
- Chirality
- Diols
- Oxidation
- Silylketone aminals
- Synthetic methods
- α-Hydroxy carbonyls
All Science Journal Classification (ASJC) codes
- Physical and Theoretical Chemistry
- Organic Chemistry