A family of iodooxazoline catalysts was developed to promote the iodine(III)-mediated α-tosyloxylation of ketone derivatives. The α-tosyloxy ketones produced are polyvalent chiral synthons. Through this study, we have unearthed a unique mode of stereoinduction from the chiral oxazoline moiety, where the stereogenic center alpha to the oxazoline oxygen atom is significant. Computational chemistry was used to rationalize the stereoinduction process. The catalysts presented promote currently among the best levels of activity and selectivity for this transformation. Evaluation of the scope of the reaction is presented
International audienceThe synthesis of α‐substituted carbonyl compounds is of great importance due t...
A new family of Lewis basic 2-pyridyl oxazolines have been developed, which can act as efficient org...
International audienceThe synthesis of α‐substituted carbonyl compounds is of great importance due t...
The development of practical methods to access chiral nonracemic α-substituted ketones is of particu...
none5siThe first catalytic asymmetric addition of TosMIC to unactivated ketones is presented. A comb...
A family of chiral iodoaniline-lactate based catalysts with C1 and C2 symmetry were efficiently synt...
An enantioselective [3+2] cyclization is reported for the construction of a chiral oxazoline skeleto...
A novel, catalytic enantioselective route to synthesize a variety of α-tertiary aryl ketones via a b...
A diastereodivergent catalytic asymmetric Michael addition of 2-oxindoles to α,β-unsaturated ketones...
Enantiopure carbonyl compounds bearing tetrasubstituted α-stereogenic centers are versatile building...
The appropriate choice of chiral catalyst and starting materials leads to the synthesis of 1,2‐oxaze...
A generic activation mode for asymmetric LUMO-lowering catalysis has been developed using the long-e...
A generic activation mode for asymmetric LUMO-lowering catalysis has been developed using the long-e...
Boron and titanium azaenolates 2 and 4, generated at 0°C and -100°C, respectively, from the opticall...
Boron and titanium azaenolates 2 and 4, generated at 0°C and -100°C, respectively, from the opticall...
International audienceThe synthesis of α‐substituted carbonyl compounds is of great importance due t...
A new family of Lewis basic 2-pyridyl oxazolines have been developed, which can act as efficient org...
International audienceThe synthesis of α‐substituted carbonyl compounds is of great importance due t...
The development of practical methods to access chiral nonracemic α-substituted ketones is of particu...
none5siThe first catalytic asymmetric addition of TosMIC to unactivated ketones is presented. A comb...
A family of chiral iodoaniline-lactate based catalysts with C1 and C2 symmetry were efficiently synt...
An enantioselective [3+2] cyclization is reported for the construction of a chiral oxazoline skeleto...
A novel, catalytic enantioselective route to synthesize a variety of α-tertiary aryl ketones via a b...
A diastereodivergent catalytic asymmetric Michael addition of 2-oxindoles to α,β-unsaturated ketones...
Enantiopure carbonyl compounds bearing tetrasubstituted α-stereogenic centers are versatile building...
The appropriate choice of chiral catalyst and starting materials leads to the synthesis of 1,2‐oxaze...
A generic activation mode for asymmetric LUMO-lowering catalysis has been developed using the long-e...
A generic activation mode for asymmetric LUMO-lowering catalysis has been developed using the long-e...
Boron and titanium azaenolates 2 and 4, generated at 0°C and -100°C, respectively, from the opticall...
Boron and titanium azaenolates 2 and 4, generated at 0°C and -100°C, respectively, from the opticall...
International audienceThe synthesis of α‐substituted carbonyl compounds is of great importance due t...
A new family of Lewis basic 2-pyridyl oxazolines have been developed, which can act as efficient org...
International audienceThe synthesis of α‐substituted carbonyl compounds is of great importance due t...