Synthesis and revised structure of garuganin III

György M. Keserü, Zoltán Dienes, Mihály Nógrádi, M. Kajtár-Peredy

Research output: Contribution to journalArticle

23 Citations (Scopus)

Abstract

Macrocyclic β-methoxy enones 6 and 1-3, i.e., garuganin III and its constitutional and stereoisomers, were synthesized using an isoxazole synthon for the introduction of the β-methoxy enone function. Ring closure was accomplished by an intramolecular Wittig reaction. Compound 6 rather than 1, as suggested previously, was found to have an 1H-NMR spectrum and a mp identical to those of garuganin III.

Original languageEnglish
Pages (from-to)6725-6728
Number of pages4
JournalJournal of Organic Chemistry
Volume58
Issue number24
Publication statusPublished - 1993

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Isoxazoles
Stereoisomerism
Nuclear magnetic resonance
garuganin

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

Keserü, G. M., Dienes, Z., Nógrádi, M., & Kajtár-Peredy, M. (1993). Synthesis and revised structure of garuganin III. Journal of Organic Chemistry, 58(24), 6725-6728.

Synthesis and revised structure of garuganin III. / Keserü, György M.; Dienes, Zoltán; Nógrádi, Mihály; Kajtár-Peredy, M.

In: Journal of Organic Chemistry, Vol. 58, No. 24, 1993, p. 6725-6728.

Research output: Contribution to journalArticle

Keserü, GM, Dienes, Z, Nógrádi, M & Kajtár-Peredy, M 1993, 'Synthesis and revised structure of garuganin III', Journal of Organic Chemistry, vol. 58, no. 24, pp. 6725-6728.
Keserü, György M. ; Dienes, Zoltán ; Nógrádi, Mihály ; Kajtár-Peredy, M. / Synthesis and revised structure of garuganin III. In: Journal of Organic Chemistry. 1993 ; Vol. 58, No. 24. pp. 6725-6728.
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