Highly enantioselective reduction of acetoacetylated meldrum's acid with fermenting baker's yeast
- 1 January 1990
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 31 (51) , 7463-7466
- https://doi.org/10.1016/s0040-4039(00)88516-0
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Baker’s Yeast Mediated Bioreduction of Prochiral Ketones Having 6-(4-Oxo-1,3-dioxinyl) GroupChemistry Letters, 1990
- Domino‐reactions: The tandem‐knoevenagel‐hetero‐diels‐alder reaction and its application in natural product synthesisJournal of Heterocyclic Chemistry, 1990
- Synthesis of the enantiomers of cis-2-methyl-5-hexanolide, the major component of the sex pheromone of the carpenter beeTetrahedron, 1985
- Microbial Asymmetric Catalysis—Enantioselective Reduction of Ketones [New Synthetic Methods (45)]Angewandte Chemie International Edition in English, 1984
- Notiz zur Darstellung von 4-Hydroxy-6-methyl-5,6-dihydro-2H-pyran-2-onMonatshefte für Chemie / Chemical Monthly, 1982
- Enantiomerically pure lactones. 3. Synthesis of and stereospecific conjugate additions to .alpha.,.beta.-unsaturated lactonesThe Journal of Organic Chemistry, 1980
- Hydrogenations of triacetic acid lactone. A new synthesis of the carpenter bee ( ) sex pheromoneTetrahedron Letters, 1980
- Meldrum's acid in organic synthesis. 2. A general and versatile synthesis of .beta.-keto estersThe Journal of Organic Chemistry, 1978
- Meldrum's acidChemical Society Reviews, 1978
- Specification of the stereospecificity of some oxido-reductases by diamond lattice sectionsPure and Applied Chemistry, 1964