An enantioselective arylation–cyclization cascade has been accomplished using a combination of diaryliodonium salts and asymmetric copper catalysis. These mild catalytic conditions provide a new strategy for the enantioselective construction of pyrroloindolines, an important alkaloid structural motif that is commonly found among biologically active natural products
Pyrrolidine and related amines undergo asymmetric A<sup>3</sup> reactions in the presence of copper ...
Pyrroloindoles are a key structural motif found in a wide number of biologically active alkaloids. I...
A copper-catalyzed enantioselective arylative semi-pinacol rearrangement of allylic alcohols using d...
Herein we report the synthesis of pyrroloindolines via a catalytic enantioselective formal [3+2] c...
The first enantioselective synthesis of five-membered N-heterocyclic allylboronates has been accompl...
Pyrroloindoline and bispyrroloindoline are a subclass of alkaloid structural motifs that commonly ex...
A catalytic enantioselective and regiodivergent arylation of alkenes is described. Chiral copper(II...
International audience"Chiral aryl cation" equivalents: The combination of diaryliodonium salts and ...
Asymmetric synthesis plays a critical role in the synthesis of modern pharmaceutical compounds which...
The asymmetric allylation of 1-pyrroline-5-carboxylic esters has been accomplished through a synergi...
α-Heteroarylpyrrolidines have been efficiently prepared via 1,3-dipolar cycloaddition between silyli...
Pyrroloindoline and unnatural tryptophan motifs are important targets for synthesis based on their i...
The (R)-BINOL·SnCl_4-catalyzed formal (3+2) cycloaddition between 3-substituted indoles and benzyl 2...
The first highly enantioselective copper-catalyzed intramolecular Ullmann C–N coupling reaction has ...
A highly enantioselective copper/<i>N</i>-heterocyclic carbene catalyzed allylic arylation with orga...
Pyrrolidine and related amines undergo asymmetric A<sup>3</sup> reactions in the presence of copper ...
Pyrroloindoles are a key structural motif found in a wide number of biologically active alkaloids. I...
A copper-catalyzed enantioselective arylative semi-pinacol rearrangement of allylic alcohols using d...
Herein we report the synthesis of pyrroloindolines via a catalytic enantioselective formal [3+2] c...
The first enantioselective synthesis of five-membered N-heterocyclic allylboronates has been accompl...
Pyrroloindoline and bispyrroloindoline are a subclass of alkaloid structural motifs that commonly ex...
A catalytic enantioselective and regiodivergent arylation of alkenes is described. Chiral copper(II...
International audience"Chiral aryl cation" equivalents: The combination of diaryliodonium salts and ...
Asymmetric synthesis plays a critical role in the synthesis of modern pharmaceutical compounds which...
The asymmetric allylation of 1-pyrroline-5-carboxylic esters has been accomplished through a synergi...
α-Heteroarylpyrrolidines have been efficiently prepared via 1,3-dipolar cycloaddition between silyli...
Pyrroloindoline and unnatural tryptophan motifs are important targets for synthesis based on their i...
The (R)-BINOL·SnCl_4-catalyzed formal (3+2) cycloaddition between 3-substituted indoles and benzyl 2...
The first highly enantioselective copper-catalyzed intramolecular Ullmann C–N coupling reaction has ...
A highly enantioselective copper/<i>N</i>-heterocyclic carbene catalyzed allylic arylation with orga...
Pyrrolidine and related amines undergo asymmetric A<sup>3</sup> reactions in the presence of copper ...
Pyrroloindoles are a key structural motif found in a wide number of biologically active alkaloids. I...
A copper-catalyzed enantioselective arylative semi-pinacol rearrangement of allylic alcohols using d...