Stereoselective Functionalization at C-2 and C-3 of the Gibberellin via an Intramolecular Free Radical Cyclization Approach

An Qi Chen*, Christine L. Willis

*Corresponding author for this work

Research output: Contribution to journalArticle (Academic Journal)peer-review

1 Citation (Scopus)

Abstract

Stereoselective functionalization at C-2 and C-3 of the gibberellin skeleton was achieved via an intramolecular free radical cyclization approach using a tethered C-19 halomethyl ester as the radical precursor.

Original languageEnglish
Pages (from-to)397-398
Number of pages2
JournalChinese Chemical Letters
Volume12
Issue number5
Publication statusPublished - May 2001

Keywords

  • Free radical cyclization
  • Gibberellin
  • Lactonization

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