Highly regioselective intramolecular biaryl coupling reaction of a phenyl benzoate derivative for the synthesis of graphislactone g

Hitoshi Abe, Takuya Matsukihira, Tomoko Fukumoto, Yoshikazu Horino, Yasuo Takeuchi, Takashi Harayama

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

The 6H-dibenzo[b,d]pyran-6-one type natural product graphislactone G was synthesized using a palladium-mediated aryl-aryl coupling reaction of the phenyl benzoate derivative. The regioselectivity in the coupling step was also investigated.

Original languageEnglish
Pages (from-to)323-326
Number of pages4
JournalHeterocycles
Volume84
Issue number1
DOIs
Publication statusPublished - Dec 22 2011

Fingerprint

Regioselectivity
Benzoates
Palladium
Biological Products
Derivatives
6H-dibenzo-(b,d)-pyran-6-one

ASJC Scopus subject areas

  • Analytical Chemistry
  • Organic Chemistry
  • Pharmacology

Cite this

Highly regioselective intramolecular biaryl coupling reaction of a phenyl benzoate derivative for the synthesis of graphislactone g. / Abe, Hitoshi; Matsukihira, Takuya; Fukumoto, Tomoko; Horino, Yoshikazu; Takeuchi, Yasuo; Harayama, Takashi.

In: Heterocycles, Vol. 84, No. 1, 22.12.2011, p. 323-326.

Research output: Contribution to journalArticle

Abe, Hitoshi ; Matsukihira, Takuya ; Fukumoto, Tomoko ; Horino, Yoshikazu ; Takeuchi, Yasuo ; Harayama, Takashi. / Highly regioselective intramolecular biaryl coupling reaction of a phenyl benzoate derivative for the synthesis of graphislactone g. In: Heterocycles. 2011 ; Vol. 84, No. 1. pp. 323-326.
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