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
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Cite this
Torii, S., Tanaka, H., Saitoh, N., Siroi, T., Sasaoka, M., & Nokami, J. (1981). Chemoselective electrolytic chlorination of methyl group of 3-methyl-3-butenoate moiety of thiazoline-azetidinone homologues. Tetrahedron Letters, 22(33), 3193-3196. https://doi.org/10.1016/S0040-4039(01)81861-X