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Intramolecular Diels–Alder route to angularly oxygenated hydrindanes. Synthesis of the functionalized bicylic skeleton present in galiellalactone.
- Source :
-
Tetrahedron . Sep2013, Vol. 69 Issue 37, p7956-7963. 8p. - Publication Year :
- 2013
-
Abstract
- Abstract: Intramolecular Diels–Alder reaction of trienones embedded in a sugar derivative with or without Me substituents on the diene part has been investigated for synthesis of hydrindanes with angular oxygen functionality. One of these adducts has been transformed to a functionalized bicyclic skeleton present in galiellalactone. [Copyright &y& Elsevier]
Details
- Language :
- English
- ISSN :
- 00404020
- Volume :
- 69
- Issue :
- 37
- Database :
- Academic Search Index
- Journal :
- Tetrahedron
- Publication Type :
- Academic Journal
- Accession number :
- 89488398
- Full Text :
- https://doi.org/10.1016/j.tet.2013.07.014