Regioselective synthesis of maturone via Lewis acid catalyzed Diels-Alder reaction

Mariko Aso, Akio Ojida, Guang Yang, Ken Kanematsu

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

Total synthesis of maturone (1) by the regioselective Dials-Alder reaction of benzofuranquinone (7) is described. Compound (7) was easily obtained by an application of the fused furan constructing method using allenic sulfonium salt (3) and cyclic 1,3-dicarbonyl compound.

Original languageEnglish
Pages (from-to)33-36
Number of pages4
JournalHeterocycles
Volume35
Issue number1
Publication statusPublished - Jan 1 1993

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Lewis Acids
Cycloaddition Reaction
Salts
furan

All Science Journal Classification (ASJC) codes

  • Organic Chemistry

Cite this

Regioselective synthesis of maturone via Lewis acid catalyzed Diels-Alder reaction. / Aso, Mariko; Ojida, Akio; Yang, Guang; Kanematsu, Ken.

In: Heterocycles, Vol. 35, No. 1, 01.01.1993, p. 33-36.

Research output: Contribution to journalArticle

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