A kinetic resolution of 1,2-diols bearing both a secondary and a primary alcohol motif through an N-heterocyclic carbene-catalyzed oxidative acylation reaction has been developed. A site- and enantioselective esterification reaction is involved for this process. Both the monoacylated diols obtained and the remaining enantioenriched 1,2-diols are versatile building blocks for the preparation of functional molecules with proven biological activities.NRF (Natl Research Foundation, S’pore)ASTAR (Agency for Sci., Tech. and Research, S’pore)MOE (Min. of Education, S’pore)Accepted versio
The kinetic resolution of racemic secondary alcohols is a fundamental method for obtaining enantiome...
An N-heterocyclic carbene (NHC)-catalyzed reaction between α-bromoenals and 2-aminoaldehydes has bee...
The concept of a synergistic double catalytic kinetic resolution (DoCKR) as described in this articl...
A kinetic resolution of 1,2-diols bearing both a secondary and a primary alcohol motif through an N-...
A kinetic resolution of 1,2-diols bearing both a secondary and a primary alcohol motif through an N-...
This paper demonstrates that the secondary hydroxyl can be functionalized in preference to the prima...
The isothiourea-catalysed acylative kinetic resolution of a range of acyclic (±)-1,2-diols using 1 m...
Optically active 1,2-diols are valuable buildings blocks in organic synthesis. In the present paper,...
We present an organocatalytic C–O-bond cross-coupling strategy to kinetically resolve racemic diols ...
International audienceThe stereocontrol of tertiary alcohols represents a recurrent challenge in org...
Le motif diol (-1,2 et -1,3) est largement répandu et essentiel dans la structure de nombreux produi...
Imidazol-2-ylidenes, a family of N-heterocyclic carbenes (NHC), are efficient catalysts in the trans...
The research described in this thesis focuses on the catalytic acylative kinetic resolution (KR) of ...
The NHC-catalyzed transformation of unsaturated aldehydes into saturated esters through an organocat...
Because of the ubiquity of the secondary carbinol subunit, the development of new methods for its en...
The kinetic resolution of racemic secondary alcohols is a fundamental method for obtaining enantiome...
An N-heterocyclic carbene (NHC)-catalyzed reaction between α-bromoenals and 2-aminoaldehydes has bee...
The concept of a synergistic double catalytic kinetic resolution (DoCKR) as described in this articl...
A kinetic resolution of 1,2-diols bearing both a secondary and a primary alcohol motif through an N-...
A kinetic resolution of 1,2-diols bearing both a secondary and a primary alcohol motif through an N-...
This paper demonstrates that the secondary hydroxyl can be functionalized in preference to the prima...
The isothiourea-catalysed acylative kinetic resolution of a range of acyclic (±)-1,2-diols using 1 m...
Optically active 1,2-diols are valuable buildings blocks in organic synthesis. In the present paper,...
We present an organocatalytic C–O-bond cross-coupling strategy to kinetically resolve racemic diols ...
International audienceThe stereocontrol of tertiary alcohols represents a recurrent challenge in org...
Le motif diol (-1,2 et -1,3) est largement répandu et essentiel dans la structure de nombreux produi...
Imidazol-2-ylidenes, a family of N-heterocyclic carbenes (NHC), are efficient catalysts in the trans...
The research described in this thesis focuses on the catalytic acylative kinetic resolution (KR) of ...
The NHC-catalyzed transformation of unsaturated aldehydes into saturated esters through an organocat...
Because of the ubiquity of the secondary carbinol subunit, the development of new methods for its en...
The kinetic resolution of racemic secondary alcohols is a fundamental method for obtaining enantiome...
An N-heterocyclic carbene (NHC)-catalyzed reaction between α-bromoenals and 2-aminoaldehydes has bee...
The concept of a synergistic double catalytic kinetic resolution (DoCKR) as described in this articl...