Abstract
A convenient procedure for the synthesis of very expensive (R)-lactic acid from relatively inexpensive (R)-alanine is described. Its subsequent conversion into a chiral dioxolanone can be carried out by using an inexpensive pivalaldehyde–tert-butanol mixture.
| Original language | English |
|---|---|
| Pages (from-to) | 1557-1559 |
| Number of pages | 3 |
| Journal | Synthesis |
| Volume | 47 |
| Issue number | 11 |
| Early online date | 2 Apr 2015 |
| DOIs | |
| Publication status | Published - 1 Jun 2015 |
Keywords
- Chiral pool
- Stereoselective synthesis
- (R)-lactic acid
- (R)-alanine
- Diazotization
- 1,3-dioxolan-4-one
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