The synthesis of fused and bridged ring systems by free radical carbocyclization. A general route to masked 1,4-diketones.
- 31 December 1983
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 24 (18), 1871-1874
- https://doi.org/10.1016/s0040-4039(00)81793-1
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Reductive cyclization of mercurial enonesThe Journal of Organic Chemistry, 1982
- (12S)-7,12-Secoishwaran-12-ol, a new type of sesquiterpene from Aristolochia indica LinnThe Journal of Organic Chemistry, 1980
- Structure of shikodonin, a unique anti-tumor spirosecokaurene diterpenoidJournal of the American Chemical Society, 1978
- Intramolecular [4+2] and [3+2] Cycloadditions in Organic SynthesisAngewandte Chemie International Edition in English, 1977
- Regiospecific alkylation of cyclic .beta.-diketone enol ethers. General synthesis of 4-alkylcyclohexenonesThe Journal of Organic Chemistry, 1973
- Cyclization of 5-hexenyl radicalsJournal of the American Chemical Society, 1972
- Interconversion of 1-phenyl-5-hexenyl, 2-phenylcyclopentylmethyl, and 3-phenylcyclohexyl radicalsJournal of the American Chemical Society, 1972
- Free-radical cyclizationsAccounts of Chemical Research, 1971
- Organotin hydrides and organic free radicalsAccounts of Chemical Research, 1968
- A Molecular Orbital Theory of Saturated Compounds. I. Ionization Potential and Bond Dissociation EnergyBulletin of the Chemical Society of Japan, 1960