Highly asymmetric bromocyclization of tryptophol by using chiral anionic phase-transfer catalyst and DABCO-derived brominating reagent is described. Optimization of the reaction conditions revealed that the reaction rate was accelerated together with improvement of enantioselectivity by addition of catalytic DABCO-derived brominating reagent. From tryptophol, 3-bromofuroindoline could be directly obtained in excellent enantioselectivities by employing this novel methodology
The effects of substituents and cavity size on catalytic efficiency of proline-rich cyclopeptoids un...
We report a chiral phosphoric acid catalyzed bromocyclization/regiodivergent reaction of racemic int...
Herein is reported the direct asymmetric addition of phenol nucleophiles to benzopyrylium salts as a...
The ability to control absolute stereochemistry is a powerful tool in organic synthesis. Given the u...
The chiral Co(III)-complex-templated Brønsted acids were found to be efficient bifunctional phase-t...
A chiral anion phase-transfer system for enantioselective halogenation is described. Highly insolubl...
Asymmetric alkene halofunctionalisation is a vibrant and rapidly expanding field. Several promising ...
A direct enantio- and diastereoselective N-acyliminium cyclization cascade through chiral phosphoric...
The first catalytic asymmetric bromonium ion-induced polyene cyclization has been achieved by using ...
This thesis describes two new phase-transfer catalysed processes, in which asymmetry is mediated via...
The defined structure of molecules bearing multiple stereogenic axes is of increasing relevance to m...
Pyrroloindoline and unnatural tryptophan motifs are important targets for synthesis based on their i...
A novel bifunctional catalyst derived from BINOL has been developed that promotes the highly enantio...
A mild and general protocol for the Pd(0)-catalyzed heteroannulation of o-bromoanilines and alkynes ...
A new and efficient synthesis of a beta-lactam that is an advanced precursor of inhibitors of thromb...
The effects of substituents and cavity size on catalytic efficiency of proline-rich cyclopeptoids un...
We report a chiral phosphoric acid catalyzed bromocyclization/regiodivergent reaction of racemic int...
Herein is reported the direct asymmetric addition of phenol nucleophiles to benzopyrylium salts as a...
The ability to control absolute stereochemistry is a powerful tool in organic synthesis. Given the u...
The chiral Co(III)-complex-templated Brønsted acids were found to be efficient bifunctional phase-t...
A chiral anion phase-transfer system for enantioselective halogenation is described. Highly insolubl...
Asymmetric alkene halofunctionalisation is a vibrant and rapidly expanding field. Several promising ...
A direct enantio- and diastereoselective N-acyliminium cyclization cascade through chiral phosphoric...
The first catalytic asymmetric bromonium ion-induced polyene cyclization has been achieved by using ...
This thesis describes two new phase-transfer catalysed processes, in which asymmetry is mediated via...
The defined structure of molecules bearing multiple stereogenic axes is of increasing relevance to m...
Pyrroloindoline and unnatural tryptophan motifs are important targets for synthesis based on their i...
A novel bifunctional catalyst derived from BINOL has been developed that promotes the highly enantio...
A mild and general protocol for the Pd(0)-catalyzed heteroannulation of o-bromoanilines and alkynes ...
A new and efficient synthesis of a beta-lactam that is an advanced precursor of inhibitors of thromb...
The effects of substituents and cavity size on catalytic efficiency of proline-rich cyclopeptoids un...
We report a chiral phosphoric acid catalyzed bromocyclization/regiodivergent reaction of racemic int...
Herein is reported the direct asymmetric addition of phenol nucleophiles to benzopyrylium salts as a...