Tetrahydrofuran Ring Opening with Acid Chlorides Catalyzed by Samarium Triiodides
- 1 July 1993
- journal article
- research article
- Published by Informa UK Limited in Synthetic Communications
- Vol. 23 (14), 1973-1977
- https://doi.org/10.1080/00397919308009856
Abstract
SmI3 acts as Lewis-acid catalysts in tetrahydrofuran ring opening reactions with acid chlorides under mild conditions.Keywords
This publication has 6 references indexed in Scilit:
- Lanthanoid(III) Trichloride–Tin(II) Chloride Mediated Cydoaddition Reaction of α,α′-Dibromo Ketones with 1,3-Dienes or EnaminesBulletin of the Chemical Society of Japan, 1989
- Samarium diiodide - A versatile reagent in organic synthesis.Journal of Synthetic Organic Chemistry, Japan, 1989
- TRICHLOROLANTHANOID(LnCl3)-CATALYZED FRIEDEL–CRAFTS ALKYLATION REACTIONSChemistry Letters, 1986
- Tetrahedron report number 213Tetrahedron, 1986
- Selective cleavage of ethers by sodium iodide-acyl chlorideTetrahedron Letters, 1982
- Studies on Acid Iodides. II. The Cleavage of Aliphatic Ethers by Acid IodidesJournal of the American Chemical Society, 1933