Synthetic studies toward the total synthesis of tedanolide: assembly of the C1-C23 carbon backbone

Chek Ming Wong, Teck Peng Loh*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

17 Citations (Scopus)

Abstract

A stereoselective assembly of the C1-C23 fragment representing the carbon backbone of tedanolide was accomplished utilizing a chiral boron reagent to effect the aldol coupling of the C1-C12 diketoester fragment with the C13-C23 aldehyde fragment.

Original languageEnglish
Pages (from-to)4485-4489
Number of pages5
JournalTetrahedron Letters
Volume47
Issue number26
DOIs
Publication statusPublished - Jun 26 2006
Externally publishedYes

ASJC Scopus Subject Areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

Keywords

  • Aldol
  • Boron reagent
  • Fragment assembly
  • Stereoselective
  • Tedanolide

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