Blay et al., 2000 - Google Patents
Synthesis of 3-Oxa-guaianolides from SantoninBlay et al., 2000
- Document ID
- 3560923021569399584
- Author
- Blay G
- Cardona L
- Garcı́a B
- Lahoz L
- Monje B
- Pedro J
- Publication year
- Publication venue
- Tetrahedron
External Links
Snippet
This article reports on the transformation of santonin into two C10-epimeric 3-oxa- guaianolides which are 8-deoxyderivatives of several natural 3-oxaguaianolides isolated from Achillea species. The synthesis involved the photochemical rearrangement of the …
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 C([C@]1(C)CC2)=CC(=O)C(C)=C1[C@@H]1[C@@H]2[C@H](C)C(=O)O1 0 title abstract description 11
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
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