Abstract
Chemoselective electrochlorination of the methyl group on the 3-methyl-3-butenoate moiety of thiazoline-azetidinone derivatives derived from penicillins G and V has been performed in a CH2Cl2-H2O-NaCl-H2SO4 -(Pt or C electrodes) system by adjusting the amount of electricity passed as well as the concentration of Cl- in the media.
Original language | English |
---|---|
Pages (from-to) | 3193-3196 |
Number of pages | 4 |
Journal | Tetrahedron Letters |
Volume | 22 |
Issue number | 33 |
DOIs | |
Publication status | Published - 1981 |
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry