The controllable cyclization reaction of indolizidinone-tethered β-amino allenes has been achieved through gold catalysis. The expected cycloisomerization of the syn-isomer sharply contrasts to the unprecedented bis(azacyclization)-spirocyclization sequence of the epimeric anti-isomer, offering highly selective access to enantiopure fused and spiranic azapolycycles.Peer Reviewe
The highly enantioselective synthesis of densely functionalized 2,3-indoline-cyclobutanes by means o...
An imino-Nazarov cyclization using α-aryl-substituted allenamides is described. This gold(I)-catalyz...
A series of cyclometallated gold(III) complexes [Au(CN)Cl2] 1a-l (HCN=arylpyridines) and a PEG-linke...
The controllable cyclization reaction of indolizidinone-tethered β-amino allenes has been achieved t...
The present study provides insights into the manner in which the configuration of β-aminoallene prec...
Alkynylaziridines carrying an aryl group could be efficiently converted into aminoallenylidene isoch...
Indole-tethered amino allenynes were chemodivergently cyclized for the controlled preparation of fus...
Axially chiral allenes are synthesized from chiral propargylamines catalyzed by KAuCl4 in high yield...
A synthesis of unconjugated (E)‐enediynes from allenyl amino alcohols is reported and their gold‐cat...
open9siThe gold-catalyzed synthesis of methylidene 2,3- cyclobutane-indoles is documented through a ...
(Azido)ynamides were efficiently converted into indoloquinolines by the use of a gold catalyst. Whil...
A reliable synthetic route to fused polycyclic indolines is documented by the development of a stere...
This thesis will focus on the development of new methodologies utilizing propargylic alcohols and ac...
Gold-catalyzed hydroarylation reaction of β-lactam-tethered allenyl indoles gives azeto-oxepino[4,5-...
The exploitation of nitrogen-functionalized reactive intermediates plays an important role in the sy...
The highly enantioselective synthesis of densely functionalized 2,3-indoline-cyclobutanes by means o...
An imino-Nazarov cyclization using α-aryl-substituted allenamides is described. This gold(I)-catalyz...
A series of cyclometallated gold(III) complexes [Au(CN)Cl2] 1a-l (HCN=arylpyridines) and a PEG-linke...
The controllable cyclization reaction of indolizidinone-tethered β-amino allenes has been achieved t...
The present study provides insights into the manner in which the configuration of β-aminoallene prec...
Alkynylaziridines carrying an aryl group could be efficiently converted into aminoallenylidene isoch...
Indole-tethered amino allenynes were chemodivergently cyclized for the controlled preparation of fus...
Axially chiral allenes are synthesized from chiral propargylamines catalyzed by KAuCl4 in high yield...
A synthesis of unconjugated (E)‐enediynes from allenyl amino alcohols is reported and their gold‐cat...
open9siThe gold-catalyzed synthesis of methylidene 2,3- cyclobutane-indoles is documented through a ...
(Azido)ynamides were efficiently converted into indoloquinolines by the use of a gold catalyst. Whil...
A reliable synthetic route to fused polycyclic indolines is documented by the development of a stere...
This thesis will focus on the development of new methodologies utilizing propargylic alcohols and ac...
Gold-catalyzed hydroarylation reaction of β-lactam-tethered allenyl indoles gives azeto-oxepino[4,5-...
The exploitation of nitrogen-functionalized reactive intermediates plays an important role in the sy...
The highly enantioselective synthesis of densely functionalized 2,3-indoline-cyclobutanes by means o...
An imino-Nazarov cyclization using α-aryl-substituted allenamides is described. This gold(I)-catalyz...
A series of cyclometallated gold(III) complexes [Au(CN)Cl2] 1a-l (HCN=arylpyridines) and a PEG-linke...