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 |
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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