A general strategy for diverse syntheses of anhydrolandomycinone, tetrangulol, and landomycinone

  • Cheng Jhe Sie
  • , Venukumar Patteti
  • , Yi Ru Yang
  • , Kwok-Kong Mong*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

A general synthetic strategy based on a protecting group-promoted CH arylation method was developed for total syntheses of anhydrolandomycinone (1), tetrangulol (2), and landomycinone (3) from the same set of starting materials.

Original languageEnglish
Pages (from-to)1885-1888
Number of pages4
JournalChemical Communications
Volume54
Issue number15
DOIs
StatePublished - 2018

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