Activation of the ketone of 5-cyclodecenones towards thermal transannular cyclization to give trans-hydroazulenols
- 13 October 1997
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 38 (41) , 7155-7158
- https://doi.org/10.1016/s0040-4039(97)01760-7
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Electrophilic and radical transannular cyclizations of 5-cyclodecenone to give either hydronaphthalene or hydroazulene productsThe Journal of Organic Chemistry, 1993
- Molecular modeling and NMR spectroscopic examination of (E)‐cyclodec‐5‐enone and its 2 ‐and 10‐methyl analogsMagnetic Resonance in Chemistry, 1993
- Total synthesis of (.+-.)-africanol and (.+-.)-isoafricanolThe Journal of Organic Chemistry, 1993
- Synthesis of either a cis- or trans-fused hydroazulenol from an allylstannane functionalized (E)-5-cyclodecenoneTetrahedron Letters, 1993
- Preparation of bicyclo[5.3.0]decan-1-ols from the tandem anionic oxy-Cope rearrangement/allylsilane cyclization of 1,2-divinylcyclohexanolsThe Journal of Organic Chemistry, 1990
- Pyridine-induced solvent shifts in the nuclear magnetic resonance spectra of hydroxylic compoundsJournal of the American Chemical Society, 1968