Efficient ring opening of 3,4-epoxyesters with alcohols to produce 4-alkoxy-3-hydroxyesters and their isomerization into 4-ketoesters using boron trifluoride as the catalyst are presented. Both transformations are simple and efficient methods for the synthesis of the above named synthetically useful compounds
International audienceThe ring opening of mono, di or tri-substituted epoxides by acetic anhydride t...
Acid catalysed reaction of carvone epoxide 2 resulted in dimericproducts 3 and 4, in contrast to the...
N-Bromosuccinimide (NBS) catalyses the ring opening of various epoxides with different thiols in CH3...
A C-3 aminolysis of epoxy homoallylic alcohols has been accomplished, which was catalyzed by a comme...
Borinic acid catalysis has been used by our group to effect ring-opening and rearrangement reactions...
By applying a catalytic amount of indium trichloride, regioselective ring-opening of epoxides to β-h...
<p>SbF<sub>3</sub> as an efficient catalyst has been used for regioselective alcoholysis, acetolysis...
Tetrabutylammonium fluoride (1) catalyses under mild conditions the opening of epoxides 2a-k with th...
Tetrabutylammonium dihydrogentrifluoride, Bu(4)N(+)H(2)F(3)(-), was found to be a very efficient cat...
Unsaturated fatty esters can be easily transformed into ketoesters through a two-step process. The h...
A study on the hydrofluorination of epoxyaldonolactones with Bu4N+H2F3- (1) under solid-liquid PTC a...
Isomerisation of 2,3-epoxy alcohols possessing an arylgroupat1 and/or 3 position, with Pd(PPh3)4 lea...
The syntheses and acid catalysed rearrangements of cis- and trans-3,4-epoxypentan-1-ols (28,22), 4,5...
Diarylborinic acids (Ar2BOH) catalyze the C3-selective ring opening of 3,4-epoxy alcohols with anili...
The stereoselective synthesis of a 2-substituted tetrahydropyran with adjacent alkoxy-bearing stereo...
International audienceThe ring opening of mono, di or tri-substituted epoxides by acetic anhydride t...
Acid catalysed reaction of carvone epoxide 2 resulted in dimericproducts 3 and 4, in contrast to the...
N-Bromosuccinimide (NBS) catalyses the ring opening of various epoxides with different thiols in CH3...
A C-3 aminolysis of epoxy homoallylic alcohols has been accomplished, which was catalyzed by a comme...
Borinic acid catalysis has been used by our group to effect ring-opening and rearrangement reactions...
By applying a catalytic amount of indium trichloride, regioselective ring-opening of epoxides to β-h...
<p>SbF<sub>3</sub> as an efficient catalyst has been used for regioselective alcoholysis, acetolysis...
Tetrabutylammonium fluoride (1) catalyses under mild conditions the opening of epoxides 2a-k with th...
Tetrabutylammonium dihydrogentrifluoride, Bu(4)N(+)H(2)F(3)(-), was found to be a very efficient cat...
Unsaturated fatty esters can be easily transformed into ketoesters through a two-step process. The h...
A study on the hydrofluorination of epoxyaldonolactones with Bu4N+H2F3- (1) under solid-liquid PTC a...
Isomerisation of 2,3-epoxy alcohols possessing an arylgroupat1 and/or 3 position, with Pd(PPh3)4 lea...
The syntheses and acid catalysed rearrangements of cis- and trans-3,4-epoxypentan-1-ols (28,22), 4,5...
Diarylborinic acids (Ar2BOH) catalyze the C3-selective ring opening of 3,4-epoxy alcohols with anili...
The stereoselective synthesis of a 2-substituted tetrahydropyran with adjacent alkoxy-bearing stereo...
International audienceThe ring opening of mono, di or tri-substituted epoxides by acetic anhydride t...
Acid catalysed reaction of carvone epoxide 2 resulted in dimericproducts 3 and 4, in contrast to the...
N-Bromosuccinimide (NBS) catalyses the ring opening of various epoxides with different thiols in CH3...