A series of 2-substituted 3-(toluenesulfonamidoalkyl)indoles was synthesized by application of (EtO)(2)POH or iodine as the catalyst, and was hydrogenated using chiral Pd catalyst, giving the 2,3-disubstituted indolines with up to 97% ee
The rhodium-catalyzed asymmetric hydrogenation of 2-substituted N-protected-indoles using monodentat...
Pd/bisphosphines complexes are highly effective catalysts for asymmetric hydrogenation of activated ...
A palladium-catalyzed asymmetric allylic alkylation of 3-substituted indoles using P/olefin ligands ...
The first highly enantioselective hydrogenation of simple indoles was developed with a Bronsted acid...
An efficient palladium-catalyzed asymmetric hydrogenation of a variety of unprotected indoles has be...
Chiral indolines are ubiquitous structural motifs in naturally occurring alkaloids and many biologic...
An efficient palladium-catalyzed asymmetric hydrogenation of a variety of unprotected indoles has be...
A concise and enantioselective procedure for the synthesis of optically active indolines has been de...
A divergent and enantioselective procedure for synthesis of 2,3-disubstituted indolines was develope...
Homogeneous Pd-catalyzed asymmetric hydrogenation of 3-phthalimido substituted quinolines was succes...
We report herein the first examples of a palladiumcatalyzed enantioselective Cacchi reaction for the...
Department of Chemistry, Acharya Nagarjuna University, Nagarjuna Nagar-522 510, Andhra Pradesh, Indi...
Asymmetric hydrogenation of heteroaromatic compounds has emerged as a promising new route to saturat...
The transition metal catalyzed asymmetric hydrogenation of unsaturated compounds arguably presents o...
Using pd(cf(3)co(2))(2)/(S,S)-f-Binaphane as the catalyst, an efficient enantioselective Synthesis o...
The rhodium-catalyzed asymmetric hydrogenation of 2-substituted N-protected-indoles using monodentat...
Pd/bisphosphines complexes are highly effective catalysts for asymmetric hydrogenation of activated ...
A palladium-catalyzed asymmetric allylic alkylation of 3-substituted indoles using P/olefin ligands ...
The first highly enantioselective hydrogenation of simple indoles was developed with a Bronsted acid...
An efficient palladium-catalyzed asymmetric hydrogenation of a variety of unprotected indoles has be...
Chiral indolines are ubiquitous structural motifs in naturally occurring alkaloids and many biologic...
An efficient palladium-catalyzed asymmetric hydrogenation of a variety of unprotected indoles has be...
A concise and enantioselective procedure for the synthesis of optically active indolines has been de...
A divergent and enantioselective procedure for synthesis of 2,3-disubstituted indolines was develope...
Homogeneous Pd-catalyzed asymmetric hydrogenation of 3-phthalimido substituted quinolines was succes...
We report herein the first examples of a palladiumcatalyzed enantioselective Cacchi reaction for the...
Department of Chemistry, Acharya Nagarjuna University, Nagarjuna Nagar-522 510, Andhra Pradesh, Indi...
Asymmetric hydrogenation of heteroaromatic compounds has emerged as a promising new route to saturat...
The transition metal catalyzed asymmetric hydrogenation of unsaturated compounds arguably presents o...
Using pd(cf(3)co(2))(2)/(S,S)-f-Binaphane as the catalyst, an efficient enantioselective Synthesis o...
The rhodium-catalyzed asymmetric hydrogenation of 2-substituted N-protected-indoles using monodentat...
Pd/bisphosphines complexes are highly effective catalysts for asymmetric hydrogenation of activated ...
A palladium-catalyzed asymmetric allylic alkylation of 3-substituted indoles using P/olefin ligands ...
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