Synthesis of neo-tanshinlactone Via the palladium-mediated intramolecular biaryl coupling reaction

Hitoshi Abe, Toshitaka Kawai, Yoshinori Komatsu, Mayu Kamimura, Yasuo Takeuchi, Yoshikazu Horino

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

Neo-tanshinlactone (1) was synthesized by the intramolecular aryl-aryl coupling reaction of the precursor ester, which was prepared from the corresponding furan carboxylic acid (13) and naphthol (3), using a palladium reagent.

Original languageEnglish
Pages (from-to)785-789
Number of pages5
JournalHeterocycles
Volume86
Issue number1
DOIs
Publication statusPublished - 2012

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Naphthols
Palladium
Carboxylic Acids
Esters
neotanshinlactone
furan

ASJC Scopus subject areas

  • Analytical Chemistry
  • Organic Chemistry
  • Pharmacology

Cite this

Synthesis of neo-tanshinlactone Via the palladium-mediated intramolecular biaryl coupling reaction. / Abe, Hitoshi; Kawai, Toshitaka; Komatsu, Yoshinori; Kamimura, Mayu; Takeuchi, Yasuo; Horino, Yoshikazu.

In: Heterocycles, Vol. 86, No. 1, 2012, p. 785-789.

Research output: Contribution to journalArticle

Abe, Hitoshi ; Kawai, Toshitaka ; Komatsu, Yoshinori ; Kamimura, Mayu ; Takeuchi, Yasuo ; Horino, Yoshikazu. / Synthesis of neo-tanshinlactone Via the palladium-mediated intramolecular biaryl coupling reaction. In: Heterocycles. 2012 ; Vol. 86, No. 1. pp. 785-789.
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AU - Horino, Yoshikazu

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