Radical annulation methodology. 2-Vinylcyclopentane derivative formation by a 3 + 2 cycloaddition reaction
- 31 December 1990
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 31 (29) , 4203-4206
- https://doi.org/10.1016/s0040-4039(00)97582-8
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- Phenylthio radical mediated synthesis of substituted 3-vinylcyclohexanones. Interruption of the ring-opening polymerization of 1,3-dioxolan-4-yl radicals.Tetrahedron Letters, 1990
- Atom-transfer addition and annulation reactions of iodomalonatesJournal of the American Chemical Society, 1989
- A strategy for radical annulation based on allyl and vinyl stannanesTetrahedron Letters, 1989
- Cyclopentane synthesis via free radical mediated addition of functionalized alkenes to substituted vinyl cyclopropanesJournal of the American Chemical Society, 1988
- Synthesis of vinylcyclopentanes from vinylcyclopropanes and alkenes promoted by benzenethiyl radicalTetrahedron Letters, 1988
- The Design and Application of Free Radical Chain Reactions in Organic Synthesis. Part 2Synthesis, 1988
- The Design and Application of Free Radical Chain Reactions in Organic Synthesis. Part 1Synthesis, 1988
- Radical reactions in organic synthesisTetrahedron, 1987
- Free radical annulation of cyclopentane ringTetrahedron Letters, 1986
- Radical annulation: a method for preparation of carbocyclesJournal of the Chemical Society, Chemical Communications, 1985