Synthesis of (±)-Jasmine Ketolactone by transannular Michael reaction

Isao Shimizu, Hiroya Nakagawa

Research output: Contribution to journalArticle

21 Citations (Scopus)

Abstract

Transannular Micheal reaction of (2E,9Z)-6-oxo-2,9-dodecadienolide gave (±)- Jasmine Ketolactone in 69 % yield.

Original languageEnglish
Pages (from-to)4957-4958
Number of pages2
JournalTetrahedron Letters
Volume33
Issue number34
DOIs
Publication statusPublished - 1992 Aug 18

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Jasminum

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Synthesis of (±)-Jasmine Ketolactone by transannular Michael reaction. / Shimizu, Isao; Nakagawa, Hiroya.

In: Tetrahedron Letters, Vol. 33, No. 34, 18.08.1992, p. 4957-4958.

Research output: Contribution to journalArticle

Shimizu, Isao ; Nakagawa, Hiroya. / Synthesis of (±)-Jasmine Ketolactone by transannular Michael reaction. In: Tetrahedron Letters. 1992 ; Vol. 33, No. 34. pp. 4957-4958.
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abstract = "Transannular Micheal reaction of (2E,9Z)-6-oxo-2,9-dodecadienolide gave (±)- Jasmine Ketolactone in 69 {\%} yield.",
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