Facile syntheses of some trans-hydroazulenes by means of electrochemical methodology coupled with base-catalyzed fragmentation reaction

Shojiro Maki, Nobuyuki Asaba, Seiji Kosemura, Shosuke Yamamura

研究成果: Article

18 引用 (Scopus)

抄録

Some phenols with an olefinic side chain have been electrolyzed under various conditions to afford tricyclo[5.3.1.01,5]undec-9-en-8,11-diones. These products were treated with potassium carbonate in methanol to give rise to the corresponding trans-hydroazulenes which are regarded as a promising synthetic intermediate of bioactive sesqui- and diterpenoids.

元の言語English
ページ(範囲)4169-4172
ページ数4
ジャーナルTetrahedron Letters
33
発行部数29
DOI
出版物ステータスPublished - 1992 7 14

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Diterpenes
Phenols
Methanol
potassium carbonate

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

これを引用

Facile syntheses of some trans-hydroazulenes by means of electrochemical methodology coupled with base-catalyzed fragmentation reaction. / Maki, Shojiro; Asaba, Nobuyuki; Kosemura, Seiji; Yamamura, Shosuke.

:: Tetrahedron Letters, 巻 33, 番号 29, 14.07.1992, p. 4169-4172.

研究成果: Article

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