En Route to Thromboxane Compounds from Carbohydrates, II. Halolactonization of 4‐c‐Branched Alkyl Hex‐2‐enopyranosides

István F. Pelyvás, Thisbe K. Lindhorst, G. Batta, Joachim Thiem

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

Bromolactonization of alkyl 4‐C‐(aminocarbonylmethyl)hex‐2‐enopyranosides 1a and 4a in nonaqueous medium results in an unexpected α‐bromination in the C‐4 side chain.

Original languageEnglish
Pages (from-to)33-37
Number of pages5
JournalLiebigs Annalen der Chemie
Volume1992
Issue number1
DOIs
Publication statusPublished - 1992

Keywords

  • Halolactonization
  • Hexenopyranoside, α‐D‐erythro‐
  • α‐Bromolactones

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Organic Chemistry

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