A FACILE PREPARATION OF TELLUROL ESTERS FROM PHENYLTELLUROTRIMETHYLSILANE AND ACYL CHLORIDES
- 5 June 1986
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 15 (6) , 977-978
- https://doi.org/10.1246/cl.1986.977
Abstract
Phenyltellurotrimethylsilane cleanly reacted with acyl chloride, giving tellurol ester in an excellent yield. The high reactivity of tellurol ester toward lithium organocuprate was demonstrated.This publication has 11 references indexed in Scilit:
- Selenoesters in organic synthesis. 2. Synthesis of α,β -unsaturated ketones.Tetrahedron Letters, 1983
- Selenoesters in organic synthesis. 1. A novel synthesis of ketones.Tetrahedron Letters, 1983
- Steroids and sex hormones. Part 262. The radical induced stannane reduction of selenoesters and selenocarbonates: A new method for the degradation of carboxylic acids to nor‐alkanes and for desoxygenation of alcohols to alkanesHelvetica Chimica Acta, 1980
- Synthesis and properties of tellurium(II) compounds: Diaryltelluroesters, ArCOTeAr′Journal of Organometallic Chemistry, 1980
- Copper(I) promoted acylation reactions. A transition metal mediated version of the Friedel-Crafts reactionJournal of the American Chemical Society, 1980
- Dimethylaluminum methylselenolate: a remarkable reagent for the preparation of active acyl-transfer agentsThe Journal of Organic Chemistry, 1978
- Macrolides. Recent Progress in Chemistry and BiochemistryAngewandte Chemie International Edition in English, 1977
- The synthesis of macrocyclic lactonesTetrahedron, 1977
- Synthesis of macrolidesTetrahedron, 1977
- Synthèses de tellurolestersBulletin des Sociétés Chimiques Belges, 1970