Abstract
Chemical conversion of penicillin into cephalosporin has been a subject of intensive studies. The problems laid on elaborating synthesis of cephalosporin are as follows: (1) construction of cephem nuclea, (2) introduction of C(3) pendants, and (3) modification of C(7) amide pendants. We found that electrolytic ene-type chlorination of thiazolineazetidinones derived from penicillins is an efficient procedure to prove problem (2) and to solve problem (3).
| Original language | English |
|---|---|
| Number of pages | 1 |
| Journal | Electrochemical Society Extended Abstracts |
| Volume | 84-1 |
| Publication status | Published - Dec 1 1984 |
ASJC Scopus subject areas
- Engineering(all)