Enantioselective synthesis of valoneic acid derivative

Hitoshi Abe, Yusuke Sahara, Yuki Matsuzaki, Yasuo Takeuchi, Takashi Harayama

Research output: Contribution to journalArticle

15 Citations (Scopus)

Abstract

The enantioselective synthesis of trimethyl octa-O-methylvaloneate (1) was accomplished using the Bringmann's 'lactone concept', which involves the intramolecular biaryl coupling reaction of a phenyl benzoate derivative and the asymmetric lactone-opening reaction.

Original languageEnglish
Pages (from-to)605-609
Number of pages5
JournalTetrahedron Letters
Volume49
Issue number4
DOIs
Publication statusPublished - Jan 21 2008

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Lactones
Derivatives
Acids
Benzoates

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Enantioselective synthesis of valoneic acid derivative. / Abe, Hitoshi; Sahara, Yusuke; Matsuzaki, Yuki; Takeuchi, Yasuo; Harayama, Takashi.

In: Tetrahedron Letters, Vol. 49, No. 4, 21.01.2008, p. 605-609.

Research output: Contribution to journalArticle

Abe, H, Sahara, Y, Matsuzaki, Y, Takeuchi, Y & Harayama, T 2008, 'Enantioselective synthesis of valoneic acid derivative', Tetrahedron Letters, vol. 49, no. 4, pp. 605-609. https://doi.org/10.1016/j.tetlet.2007.11.154
Abe, Hitoshi ; Sahara, Yusuke ; Matsuzaki, Yuki ; Takeuchi, Yasuo ; Harayama, Takashi. / Enantioselective synthesis of valoneic acid derivative. In: Tetrahedron Letters. 2008 ; Vol. 49, No. 4. pp. 605-609.
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