A binary catalyst system for the enantioselective bromocycloetherification of 5-arylpentenols is described. The combination of an achiral Lewis base and a chiral Brønsted acid affords good enantioselectivities for the cyclization of <i>Z</i> configured 5-arylpentenols to form bromomethyltetrahydrofurans. The constitutional site selectivity is highly dependent upon the aromatic substituent and the configuration of the double bond
A general protocol is described for inducing enantioselective halolactonizations of unsaturated carb...
A rapid development of metal-free, main group compounds for small molecule activation and as hydroge...
The first catalytic asymmetric bromonium ion-induced polyene cyclization has been achieved by using ...
A binary catalyst system for the enantioselective bromocycloetherification of 5-arylpentenols is des...
A novel bifunctional catalyst derived from BINOL has been developed that promotes the highly enantio...
A novel bifunctional catalyst derived from BINOL has been developed that promotes the highly enantio...
The stereochemical stability of bromonium and chloronium ions has been investigated in the context o...
Asymmetric bromolactonization reactions of δ-unsaturated carboxylic acids have been investigated in ...
In this study a highly efficient catalyst has been observed for tandem solvent free enantioselective...
In the field of catalytic, asymmetric synthesis, there is a grow-ing emphasis on multifunctional sys...
The field of asymmetric catalysis has witnessed tremendous development since its discovery, and this...
The enantioselective iodolactonizations of a series of diversely substituted olefinic carboxylic aci...
The enantioselective iodolactonizations of a series of diversely substituted olefinic carboxylic aci...
The enantioselective iodolactonizations of a series of diversely substituted olefinic carboxylic aci...
A chiral phosphoric acid catalyzed enantioselective bromocyclization of olefins is described. Variou...
A general protocol is described for inducing enantioselective halolactonizations of unsaturated carb...
A rapid development of metal-free, main group compounds for small molecule activation and as hydroge...
The first catalytic asymmetric bromonium ion-induced polyene cyclization has been achieved by using ...
A binary catalyst system for the enantioselective bromocycloetherification of 5-arylpentenols is des...
A novel bifunctional catalyst derived from BINOL has been developed that promotes the highly enantio...
A novel bifunctional catalyst derived from BINOL has been developed that promotes the highly enantio...
The stereochemical stability of bromonium and chloronium ions has been investigated in the context o...
Asymmetric bromolactonization reactions of δ-unsaturated carboxylic acids have been investigated in ...
In this study a highly efficient catalyst has been observed for tandem solvent free enantioselective...
In the field of catalytic, asymmetric synthesis, there is a grow-ing emphasis on multifunctional sys...
The field of asymmetric catalysis has witnessed tremendous development since its discovery, and this...
The enantioselective iodolactonizations of a series of diversely substituted olefinic carboxylic aci...
The enantioselective iodolactonizations of a series of diversely substituted olefinic carboxylic aci...
The enantioselective iodolactonizations of a series of diversely substituted olefinic carboxylic aci...
A chiral phosphoric acid catalyzed enantioselective bromocyclization of olefins is described. Variou...
A general protocol is described for inducing enantioselective halolactonizations of unsaturated carb...
A rapid development of metal-free, main group compounds for small molecule activation and as hydroge...
The first catalytic asymmetric bromonium ion-induced polyene cyclization has been achieved by using ...