Acetoxylation of β-lactams with lead(IV) acetate

Le Thanh Giang, J. Fetter, M. Kajtár-Peredy, Károly Lempert, Gábor Czira

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

1-(4-Methoxyphenyl)azetidin-2-ones 5a-5g were acetoxylated by lead(IV) acetate to afford the corresponding compounds 6a, 6b, 6c' and 6d-6g. In the d series elimination products 9 and 10 were also formed. Ring homologue 7a afforded the hydroxylated derivative 8'a.

Original languageEnglish
Pages (from-to)13741-13748
Number of pages8
JournalTetrahedron
Volume55
Issue number48
DOIs
Publication statusPublished - Nov 26 1999

Fingerprint

Lactams
Acetates
Derivatives
Lead
lead acetate

Keywords

  • Azetidin-2-ones
  • Oxidative Acetoxylation
  • Pyrrolidin-2-ones

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Acetoxylation of β-lactams with lead(IV) acetate. / Giang, Le Thanh; Fetter, J.; Kajtár-Peredy, M.; Lempert, Károly; Czira, Gábor.

In: Tetrahedron, Vol. 55, No. 48, 26.11.1999, p. 13741-13748.

Research output: Contribution to journalArticle

Giang, Le Thanh ; Fetter, J. ; Kajtár-Peredy, M. ; Lempert, Károly ; Czira, Gábor. / Acetoxylation of β-lactams with lead(IV) acetate. In: Tetrahedron. 1999 ; Vol. 55, No. 48. pp. 13741-13748.
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