Ring opening rections of vinyl cyclopropanes with para toluene sulphonyl iodide.
- 1 January 1988
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 29 (33) , 4173-4176
- https://doi.org/10.1016/s0040-4039(00)80448-7
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- .alpha.-Haloalkanesulfonyl bromides in organic synthesis. 5. Versatile reagents for the synthesis of conjugated polyenes, enones, and 1,3-oxathiole 1,1-dioxidesJournal of the American Chemical Society, 1986
- The Vinylcyclopropane–CyclopenteneRearrangementPublished by Wiley ,1985
- Free-radical clocksAccounts of Chemical Research, 1980
- Syntheses a l'aide de sulfones VII. Ouverture stereoselective d'alcools cyclopropaniques tertiaires.Tetrahedron Letters, 1974
- General 1,5-diene synthesis. Application to the synthesis of squaleneThe Journal of Organic Chemistry, 1974
- Synthetic proof of the structure of a proposed codling moth sex pheromoneTetrahedron Letters, 1973
- Additions of Tributyltin Hydride to TerpenesThe Journal of Organic Chemistry, 1970
- A highly stereoselective synthesis of the racemic juvenile hormoneJournal of the American Chemical Society, 1968
- A highly stereoselective synthesis of trans-trisubstituted olefinic bondsJournal of the American Chemical Society, 1968
- Jodide aromatischer SulfonsäurenEuropean Journal of Inorganic Chemistry, 1891