Synthetic applications of the tandem aldol condensation-radical cyclization sequence. A new and highly convergent method for the annulation of carbocycles
- 31 December 1985
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 26 (52) , 6431-6434
- https://doi.org/10.1016/s0040-4039(00)99019-1
Abstract
No abstract availableKeywords
This publication has 2 references indexed in Scilit:
- Tandem conjugate addition. Aldol reactions employing 9-(phenylseleno)-9-borabicyclononane: a novel method for effecting formal aldol condensations at the .alpha.-carbon of .alpha.,.beta.-unsaturated ketonesThe Journal of Organic Chemistry, 1985
- Aldol Reaction of Aluminium Enolate Resulting from 1,4-Addition of R2AlX to α,β-Unsaturated Carbonyl Compound. A 1-Acylethenyl Anion EquivalentBulletin of the Chemical Society of Japan, 1981