A microbially-based approach for the synthesis of chiral secondary alcohols bearing the difluoromethyl or chlorodifluoromethyl group
- 5 March 1992
- journal article
- Published by Elsevier in Journal of Fluorine Chemistry
- Vol. 56 (3), 271-284
- https://doi.org/10.1016/s0022-1139(00)81174-4
Abstract
No abstract availableThis publication has 17 references indexed in Scilit:
- A microbially based approach for the preparation of chiral molecules possessing the trifluoromethyl groupThe Journal of Organic Chemistry, 1987
- Novel Ferroelectricity in Fluorinated Ferroelectric Liquid CrystalJapanese Journal of Applied Physics, 1987
- Synthetic approach to versatile chiral molecules containing a fluorine atomThe Journal of Organic Chemistry, 1986
- Microbial approach to the practical monofluorinated chiral synthonsThe Journal of Organic Chemistry, 1986
- Di‐ and Trifluoro‐Substituted Dilithium Compounds for Organic SynthesesAngewandte Chemie International Edition in English, 1986
- Nichtproteinogene Aminosäuren, II. Synthese und absolute Konfigurationsermittlung von (2S,4S)‐(‐)‐ und (2S,4R)‐(+)‐5,5,5‐TrifluorleucinEuropean Journal of Organic Chemistry, 1985
- Synthesis of (+)s-α-perfluoroethyl-α-hydroxyphenyl acetic acid and highly effective auxiliaries for use in asymmetric inductionTetrahedron Letters, 1984
- Asymmetric Reduction of Trifluoromethyl and Methyl Ketones by Yeast; An Improved MethodSynthesis, 1983
- Suicide substrates: mechanism-based enzyme inactivatorsTetrahedron, 1982
- Mechanistic studies with vinylglycine and .beta.-haloaminobutyrates as substrates for cystathionine .gamma.-synthetase from Salmonella typhimuriumBiochemistry, 1979