A copper(I) complex of i-Pr-pybox-diPh has been found to be an efficient catalyst for an enantioselective one-pot three-component synthesis of propargylamines from aldehydes, amines, and alkynes. The reaction has been applied to a wide variety of aromatic aldehydes with excellent yields (up to 99%) and enantiomeric excesses (up to 99% ee). A transition-state model has been proposed to explain the stereochemical outcome of the reaction
The enantioselective synthesis of substituted pyrrolidines through a mild Lewis-acid catalyzed three...
The stereoselective addition of aryl and alkylacetylene derivatives to immines was the first reactio...
A copper catalyst with a chiral pyridine-2,6-bisoxazoline (pybox) ligand was used to convert a varie...
A one-pot three-component coupling of aldehydes and amines in presence of terminal alkynes has been ...
The first copper-catalyzed direct three-component coupling reaction of aldehydes, alkynes, and hydro...
A three-component stereoselective reaction between an aldehyde, an amine and phenylacetylene to affo...
An efficient route to enantioenriched propargylamines via a three-component alkynylation reaction us...
[[abstract]]An efficient three-component coupling reaction of aldehyde, pyrrolidine and tributylstan...
The stereoselective addition of aryl- and alkylacetylene derivatives to imines was studied. The reac...
A variety of unique small molecule families were created through copper-catalyzed three-component co...
An easy and versatile Cu-catalyzed propargylic substitution process is presented. Using easily prepa...
[{Rh(μ-Cl)(H)2(IPr)}2] (IPr = 1,3-bis-(2,6-diisopropylphenyl)imidazole-2-ylidene) was found to be an...
Propargylamines are synthesized in high yields via a gold(III) (C^N) complex-catalyzed three-compone...
The stereoselective addition of phenyl acetylene to imines, catalysed by chiral bis-amine-Cu(I) comp...
An efficient three-component coupling of aldehydes, amines and alkynes to prepare propargylamines, i...
The enantioselective synthesis of substituted pyrrolidines through a mild Lewis-acid catalyzed three...
The stereoselective addition of aryl and alkylacetylene derivatives to immines was the first reactio...
A copper catalyst with a chiral pyridine-2,6-bisoxazoline (pybox) ligand was used to convert a varie...
A one-pot three-component coupling of aldehydes and amines in presence of terminal alkynes has been ...
The first copper-catalyzed direct three-component coupling reaction of aldehydes, alkynes, and hydro...
A three-component stereoselective reaction between an aldehyde, an amine and phenylacetylene to affo...
An efficient route to enantioenriched propargylamines via a three-component alkynylation reaction us...
[[abstract]]An efficient three-component coupling reaction of aldehyde, pyrrolidine and tributylstan...
The stereoselective addition of aryl- and alkylacetylene derivatives to imines was studied. The reac...
A variety of unique small molecule families were created through copper-catalyzed three-component co...
An easy and versatile Cu-catalyzed propargylic substitution process is presented. Using easily prepa...
[{Rh(μ-Cl)(H)2(IPr)}2] (IPr = 1,3-bis-(2,6-diisopropylphenyl)imidazole-2-ylidene) was found to be an...
Propargylamines are synthesized in high yields via a gold(III) (C^N) complex-catalyzed three-compone...
The stereoselective addition of phenyl acetylene to imines, catalysed by chiral bis-amine-Cu(I) comp...
An efficient three-component coupling of aldehydes, amines and alkynes to prepare propargylamines, i...
The enantioselective synthesis of substituted pyrrolidines through a mild Lewis-acid catalyzed three...
The stereoselective addition of aryl and alkylacetylene derivatives to immines was the first reactio...
A copper catalyst with a chiral pyridine-2,6-bisoxazoline (pybox) ligand was used to convert a varie...