Abstract
Addition of Grignard and organolithium reagents to O-phenethyl aldoximes in the presence of boron trifluoride etherate gives secondary hydroxylamines in 21-84% yield with 38-95% diastereomeric excess.
| Original language | English |
|---|---|
| Pages (from-to) | 445-446 |
| Number of pages | 2 |
| Journal | Synlett |
| Issue number | 5 |
| Publication status | Published - May 1995 |
Keywords
- ASYMMETRIC ADDITION
- CHIRAL OXIME ETHER
- HYDROXYLAMINE
- ALDEHYDE-SAMP HYDRAZONES
- ALPHA-IMINO ESTERS
- OXIME ETHERS
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