Using (-)-menthol as an auxiliary, three chiral vinylic epoxides have been synthesised from the corresponding glycidic esters via α-hydroxy-β,γ-unsaturated esters. Enzymatic resolution of α-acetoxy-β,γ-unsaturated esters using PLAP leads to optically active α-hydroxy- β,γ-unsaturated esters
Both enantiomers of cis-(+/-)-2,3-epoxyheptane 1a, cis-3,4-epoxyheptane 1b, cis-3,4-epoxynonane 1c, ...
The synthesis of a new class of epoxide derivatives from prochiral vinylidene bisphosphonate (VBP) p...
The efficient enzymatic synthesis of enantiopure 2,3-epoxypropanol (glycidol) has been achieved. The...
Glycidic esters, upon isomerisation with BF3.Et2O yield α-hydroxy-β,γ-unsaturated esters. These are ...
Enantiomerically pure terminal 1,2-diols are important synthetic intermediates.1 A number of synthet...
The synthesis of a number of β-amino tertiary alcohols has been achieved via ring-opening of an unsy...
The hydrolytic ring opening of epoxides is an important biosynthetic transformation and is also appl...
Using chiral alcohol precursors, a number of chiral vinyl ethers were prepared by mercuric acetate-c...
Epoxides are attractive intermediates for producing chiral compounds. Important biocatalytic reactio...
An overview of the synthesis and applications of chiral 2,3-epoxy alcohols containing unsaturated ch...
Optically active epoxy alcohol, (R)-2-butyryloxymethylglycidol 3 which is the precursor of a tert-al...
Use of Chiral Separations for the Determination of Enzyme Enantioselectivity Jiří Břicháč Enantiosel...
This work describes the development of enantioselective oxidation reactions of carbonyl compounds us...
"Asymmetric epoxidation holds a venerable place in the organic chemistry since chiral epoxy products...
Enantiomerically enriched trans-2,3-epoxyamides 3 were prepared by the reaction of aldehydes 2 with ...
Both enantiomers of cis-(+/-)-2,3-epoxyheptane 1a, cis-3,4-epoxyheptane 1b, cis-3,4-epoxynonane 1c, ...
The synthesis of a new class of epoxide derivatives from prochiral vinylidene bisphosphonate (VBP) p...
The efficient enzymatic synthesis of enantiopure 2,3-epoxypropanol (glycidol) has been achieved. The...
Glycidic esters, upon isomerisation with BF3.Et2O yield α-hydroxy-β,γ-unsaturated esters. These are ...
Enantiomerically pure terminal 1,2-diols are important synthetic intermediates.1 A number of synthet...
The synthesis of a number of β-amino tertiary alcohols has been achieved via ring-opening of an unsy...
The hydrolytic ring opening of epoxides is an important biosynthetic transformation and is also appl...
Using chiral alcohol precursors, a number of chiral vinyl ethers were prepared by mercuric acetate-c...
Epoxides are attractive intermediates for producing chiral compounds. Important biocatalytic reactio...
An overview of the synthesis and applications of chiral 2,3-epoxy alcohols containing unsaturated ch...
Optically active epoxy alcohol, (R)-2-butyryloxymethylglycidol 3 which is the precursor of a tert-al...
Use of Chiral Separations for the Determination of Enzyme Enantioselectivity Jiří Břicháč Enantiosel...
This work describes the development of enantioselective oxidation reactions of carbonyl compounds us...
"Asymmetric epoxidation holds a venerable place in the organic chemistry since chiral epoxy products...
Enantiomerically enriched trans-2,3-epoxyamides 3 were prepared by the reaction of aldehydes 2 with ...
Both enantiomers of cis-(+/-)-2,3-epoxyheptane 1a, cis-3,4-epoxyheptane 1b, cis-3,4-epoxynonane 1c, ...
The synthesis of a new class of epoxide derivatives from prochiral vinylidene bisphosphonate (VBP) p...
The efficient enzymatic synthesis of enantiopure 2,3-epoxypropanol (glycidol) has been achieved. The...