Synthese funktionalisierter hydroazulene - ein neuer zugang zum lactaran-gerüst
- 1 January 1994
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 50 (32) , 9657-9670
- https://doi.org/10.1016/s0040-4020(01)85534-4
Abstract
No abstract availableKeywords
This publication has 35 references indexed in Scilit:
- Synthesis of New Terpene Skeletons by Chemical Cyclization of Epoxy OlefinsEuropean Journal of Organic Chemistry, 1994
- A concise route to the tetracyclic core of phorbolTetrahedron, 1994
- Stereoselective synthesis of (±)-clavukerin A and (±)-isoclavukerin A based on palladium-catalyzed reductive cleavage of alkenylcyclopropanes with formic acidTetrahedron Letters, 1994
- Novel cyclizations involving vinyl sulfones: Stereoselective construction of perhydroazulenes and trans-hydrindanes.Tetrahedron Letters, 1993
- (Trimethylsilyl)methyl allylic sulfones in intramolecular 4 + 3 cycloadditionsThe Journal of Organic Chemistry, 1993
- Stereocontrolled double ring expansion of fused allylidenecyclopropanes. A novel route to hydroazulenes and other fused bicyclic systemsJournal of the American Chemical Society, 1993
- Allylsilane-based annulations. Direct stereoselective syntheses of (.+-.)-graveolide and (.+-.)-aromaticinThe Journal of Organic Chemistry, 1993
- Palladium-catalysed Synthesis of PerhydroazulenesSynlett, 1993
- The Structure of a Novel Fungal Sesquiterpene, Elucidated by Spectral and Computational Methods.Acta Chemica Scandinavica, 1988
- The Sesquiterpenes of Lactarius vellereus and Their Role in a Proposed Chemical Defense SystemJournal of Natural Products, 1985