A catalytic decarbonylation reaction for epoxyaldehydes is reported. This reaction may be sequentially used with known asymmetric methods to access optically active mono- and disubstituted terminal epoxides, as illustrated for a key example
The epoxide function plays an important role in metabolic processes. It is surprising therefore that...
In this article the first enantioselective epoxidation reaction of acyclic and cyclic 2-arylidene-1,...
Modern epoxidation methods are able to create two adjacent stereocenters with very high enantioselec...
A catalytic decarbonylation reaction for epoxyaldehydes is reported. This reaction may be sequential...
We report the regioselective carbonylation of 2,2-disubstituted epoxides to β,β-disubstituted β-lact...
Reaction of a variety of epoxides with DMSO-Oxalyl chloride in the presence of a catalytic amount of...
A systematically varied series of conformationally restricted ketones, readily prepared from N-acety...
Enantiomerically pure terminal 1,2-diols are important synthetic intermediates.1 A number of synthet...
The area of asymmetric epoxidation of ,-unsaturated carbonyl compounds is extensively studied owing ...
Epoxides are versatile building blocks in organic chemistry due to their inherent reactivity and syn...
Epoxides are attractive intermediates for producing chiral compounds. Important biocatalytic reactio...
"Asymmetric epoxidation holds a venerable place in the organic chemistry since chiral epoxy products...
This thesis presents our investigations into the catalytic asymmetric epoxidation of alkenes. An int...
In this Minireview recent advances in the asymmetric reactions of meso and racemic epoxides promoted...
1. Catalyst used in the kinetic resolution of racemic, terminal epoxides yielding a chiral diol and ...
The epoxide function plays an important role in metabolic processes. It is surprising therefore that...
In this article the first enantioselective epoxidation reaction of acyclic and cyclic 2-arylidene-1,...
Modern epoxidation methods are able to create two adjacent stereocenters with very high enantioselec...
A catalytic decarbonylation reaction for epoxyaldehydes is reported. This reaction may be sequential...
We report the regioselective carbonylation of 2,2-disubstituted epoxides to β,β-disubstituted β-lact...
Reaction of a variety of epoxides with DMSO-Oxalyl chloride in the presence of a catalytic amount of...
A systematically varied series of conformationally restricted ketones, readily prepared from N-acety...
Enantiomerically pure terminal 1,2-diols are important synthetic intermediates.1 A number of synthet...
The area of asymmetric epoxidation of ,-unsaturated carbonyl compounds is extensively studied owing ...
Epoxides are versatile building blocks in organic chemistry due to their inherent reactivity and syn...
Epoxides are attractive intermediates for producing chiral compounds. Important biocatalytic reactio...
"Asymmetric epoxidation holds a venerable place in the organic chemistry since chiral epoxy products...
This thesis presents our investigations into the catalytic asymmetric epoxidation of alkenes. An int...
In this Minireview recent advances in the asymmetric reactions of meso and racemic epoxides promoted...
1. Catalyst used in the kinetic resolution of racemic, terminal epoxides yielding a chiral diol and ...
The epoxide function plays an important role in metabolic processes. It is surprising therefore that...
In this article the first enantioselective epoxidation reaction of acyclic and cyclic 2-arylidene-1,...
Modern epoxidation methods are able to create two adjacent stereocenters with very high enantioselec...
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