A facile and selective synthesis of β-keto esters via zeolite catalysed transesterification
- 1 January 1996
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- No. 6,p. 707-708
- https://doi.org/10.1039/cc9960000707
Abstract
Crystalline microporous aluminosilicates (zeolites) efficiently catalyse the transesterification of β-keto esters with high selectivity under environmentally safe reaction conditions.Keywords
This publication has 19 references indexed in Scilit:
- Mastering .beta.-Keto EstersChemical Reviews, 1995
- Facile synthesis of β-ketoesters mediated by SmI2: Reformatsky reaction type selfcondensationTetrahedron Letters, 1995
- TransesterificationChemical Reviews, 1993
- A Safe, Economical Method for the Preparation of β-Oxo EstersSynthesis, 1993
- Synthesis of .beta.-keto esters by the Reformatsky reaction of 3-acyloxazolidin-2-ones and -thiazolidine-2-thionesThe Journal of Organic Chemistry, 1993
- Synthesis of Podophyllotoxin and Related CompoundsSynthesis, 1992
- A selective method for the direct conversion of aldehydes into .beta.-keto esters with ethyl diazoacetate catalyzed by tin(II) chlorideThe Journal of Organic Chemistry, 1989
- Transesterification of 3-oxo esters with allylic alcoholsThe Journal of Organic Chemistry, 1988
- The Rearrangement of Allyl-Type Esters of β-Keto AcidsJournal of the American Chemical Society, 1943
- 131. Addition of αβ-unsaturated alcohols to the active methylene group. Part I. The action of ethyl acetoacetate on linalool and geraniolJournal of the Chemical Society, 1940