A substrate-independent selective generation of enolates over homoenolate equivalents in NHC-catalyzed reactions of enals and chalcones is disclosed. Acid co-catalysts play vital roles in control of the reaction pathways, allowing for individual access to diverse products from identical substrates
The facile synthesis of 1,3,4-trisubstituted cyclopentenes via homoenolate annulation of enals with ...
A strategy to control the switch between a non‐cycloaddition reaction and a cycloaddition reaction o...
An oxidative γ-functionalization of enals under N-heterocyclic carbene (NHC) catalysis to give unsat...
A substrate-independent selective generation of enolates over homoenolate equivalents in NHC-catalyz...
My Ph.D research mainly focuses on developing new reactions and synthetic methods via oxidative N-He...
Homoenolate is a reactive intermediate that possesses an anionic or nucleophilic carbon β to a carbo...
The first N-Heterocyclic Carbene (NHC) mediated activation of stable carboxylate esters to generate ...
In this thesis, we studied the application of nucleophilic NHC-derived acyl anion, homoenolate or az...
Nucleophilic heterocyclic carbene (NHC)-catalyzed annulation of enals proceeds with variety of 1,2-d...
The first N-Heterocyclic Carbene (NHC) mediated activation of stable carboxylate esters to generate ...
A direct α-functionalization of simple aldehydes under <i>N</i>-Heterocyclic Carbene (NHC) catalysis...
The first successful generation of cis-homoenolate equivalents from cis-enals under the catalysis of...
A direct α-functionalization of simple aldehydes under N-Heterocyclic Carbene (NHC) catalysis and di...
An electron-withdrawing group was introduced to the α-position of chalcones, and the resulting alkyl...
New trick for an old cat.: Triazolium-based N-heterocyclic carbenes (NHCs) catalyze the selective ge...
The facile synthesis of 1,3,4-trisubstituted cyclopentenes via homoenolate annulation of enals with ...
A strategy to control the switch between a non‐cycloaddition reaction and a cycloaddition reaction o...
An oxidative γ-functionalization of enals under N-heterocyclic carbene (NHC) catalysis to give unsat...
A substrate-independent selective generation of enolates over homoenolate equivalents in NHC-catalyz...
My Ph.D research mainly focuses on developing new reactions and synthetic methods via oxidative N-He...
Homoenolate is a reactive intermediate that possesses an anionic or nucleophilic carbon β to a carbo...
The first N-Heterocyclic Carbene (NHC) mediated activation of stable carboxylate esters to generate ...
In this thesis, we studied the application of nucleophilic NHC-derived acyl anion, homoenolate or az...
Nucleophilic heterocyclic carbene (NHC)-catalyzed annulation of enals proceeds with variety of 1,2-d...
The first N-Heterocyclic Carbene (NHC) mediated activation of stable carboxylate esters to generate ...
A direct α-functionalization of simple aldehydes under <i>N</i>-Heterocyclic Carbene (NHC) catalysis...
The first successful generation of cis-homoenolate equivalents from cis-enals under the catalysis of...
A direct α-functionalization of simple aldehydes under N-Heterocyclic Carbene (NHC) catalysis and di...
An electron-withdrawing group was introduced to the α-position of chalcones, and the resulting alkyl...
New trick for an old cat.: Triazolium-based N-heterocyclic carbenes (NHCs) catalyze the selective ge...
The facile synthesis of 1,3,4-trisubstituted cyclopentenes via homoenolate annulation of enals with ...
A strategy to control the switch between a non‐cycloaddition reaction and a cycloaddition reaction o...
An oxidative γ-functionalization of enals under N-heterocyclic carbene (NHC) catalysis to give unsat...