A convenient synthesis of C(2)-substituted cephalosporins

S. Torii, H. Tanaka, N. Saitoh

Research output: Contribution to journalArticlepeer-review

6 Citations (Scopus)


Replacement of the C(2)-substituents of 2-acetoxy- or 2-methoxycephalosporin with nucleophiles was performed efficiently in dichloromethane in the presence of acid-catalysts, affording cephalosporins bearing heteroaromatic moieties, sulfenyl, and alkoxyl groups at the C(2)-position.

Original languageEnglish
Pages (from-to)2185-2186
Number of pages2
JournalBulletin of the Chemical Society of Japan
Issue number7
Publication statusPublished - Jan 1 1983

ASJC Scopus subject areas

  • Chemistry(all)


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