Stereoselective synthesis of (±)-cedranediol via intramolecular double michael reaction
- 21 July 1997
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 38 (29) , 5197-5200
- https://doi.org/10.1016/s0040-4039(97)01126-x
Abstract
No abstract availableThis publication has 17 references indexed in Scilit:
- Domino Reactions in Organic SynthesisChemical Reviews, 1996
- Stereoselective Construction of Copaborneol and Longiborneol Frameworks by Intramolecular Double Michael ReactionThe Journal of Organic Chemistry, 1996
- Syntheses of Polycyclic Natural Products Employing the Intramolecular Double Michael ReactionAngewandte Chemie International Edition in English, 1993
- Total synthesis of (±)-pentalenic acid via intramolecular double Michael reactionJournal of the Chemical Society, Chemical Communications, 1987
- The intramolecular diels-alder reactions of (E)- and (Z)-methyl 5-12-methyl-4-(trihethylsilyloxy)-2,4-cyclopentadienyl]-2-pentenoate. A stereoselective synthesis of (±)-sativeneTetrahedron, 1986
- A new strategy for the synthesis of spiro ketalsThe Journal of Organic Chemistry, 1983
- Total synthesis of (±)-8S, 14-cedranediolTetrahedron, 1983
- Total synthesis of (.+-.)-cedrol and (.+-.)-cedrene via an intramolecular Diels-Alder reactionThe Journal of Organic Chemistry, 1978
- Synthesen in der reihe der tricyclischen sesquiterpene synthese von 4-desmethyl-11-norseychellanonTetrahedron Letters, 1978
- Some new cedrane derivatives from Juniperus foetidissima willd.Tetrahedron, 1968