A Mild and Efficient Alumina-Promoted Synthesis of t-Butyl Esters
- 1 July 1990
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 20 (13) , 2033-2040
- https://doi.org/10.1080/00397919008053134
Abstract
A wide variety of aliphatic acid chlorides including an optically active one has been efficiently converted to their t-butyl esters under very mild reaction conditions by employing activated alumina as a catalyst.Keywords
This publication has 7 references indexed in Scilit:
- Reactions of unsaturated compounds with iodine and bromine on .gamma. aluminaThe Journal of Organic Chemistry, 1988
- Chemical Reactions on ClaysScience, 1987
- A novel and efficient synthesis of 5-substituted and 5,6-disubstituted 4-methylcoumarins using organocerium(III) reagentsTetrahedron Letters, 1985
- a highly stereoselective synthesis of carbocyclic compounds by the michael induced intramolecular alkylation a stereocontrol of extracyclic chiral centersTetrahedron Letters, 1985
- Organic Reactions at Alumina SurfacesAngewandte Chemie International Edition in English, 1978
- Reaction of lithio tert-butyl trimethylsilylacetate with acyl imidazoles. A synthesis of β-keto esters.Tetrahedron Letters, 1976
- Condensation of tert-butyl .alpha.-lithioisobutyrate with acid chlorides. Synthesis for .beta.-keto acids and ketonesThe Journal of Organic Chemistry, 1974