Synthesis of (±)-recifeiolide and its homologs via acetylenic lactones

Article abstract of DOI:10.1080/00397919608003797

The title compounds (7c,d) have been prepared by the Z to E isomerization (NaNO₂, HNO₃) of the corresponding Z-lactones (6c,d), which are stereoselectively available (H₂, Lindlar cat.) from the acetylenic lactones 4a-d, prepared earlier from cycloalkanones.

Full text of DOI:10.1080/00397919608003797

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Synthesis of (±)-Recifeiolide
and Its Homologs via Acetylenic
Lactones
a
a
Jaswant Rai Mahajan & Inês Sabioni Resck
a
Departament of Chemistry , University of Brasília ,
0.910–900, Brasília-DF, Brazil
7
Published online: 21 Aug 2006.
To cite this article: Jaswant Rai Mahajan & Inês Sabioni Resck (1996) Synthesis of (±)-
Recifeiolide and Its Homologs via Acetylenic Lactones, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry, 26:20,
3809-3819, DOI: 10.1080/00397919608003797
To link to this article: http://dx.doi.org/10.1080/00397919608003797
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