A domino synthesis of 5,12-dihydroindolo[2,1-<i>b</i>]quinazoline derivatives via copper-catalyzed Ullmann-type intermolecular C–C and intramolecular C–N couplings is reported. Good yields of various 5,12-dihydroindolo[2,1-<i>b</i>]quinazoline derivatives were obtained. Reaction scopes, limitations, and the reaction mechanism are discussed
The first highly enantioselective copper-catalyzed intramolecular Ullmann C–N coupling reaction has ...
International audienceA copper-catalyzed three-component assembly of cyanamides, 2-cyanoarylboronic ...
A convenient catalytic protocol for efficiently constructing indoline-fused tetrahydroisoquinolines ...
A convenient CuI/L-proline-catalyzed, two-step one-pot method has been developed for the preparation...
An efficient three-component domino reaction of 2-bromoaldehydes, benzylamines, and sodium azide has...
Highly selective and convenient synthesis of indolo[1,2-<i>c</i>]quinazolines and 11<i>H</i>-indol...
Herein, a copper(II)-catalyzed dearomative cyclization amination of N-(2-aminobenzoyl) indoles is pr...
A synthetic approach to quinindoline derivatives by the Cu-catalyzed dual cyclization has been devel...
A novel copper-catalyzed synthesis of quinazolinones from easily available 2-arylindoles and amines ...
[[abstract]]An efficient and novel procedure for a copper catalyzed domino coupling reaction has bee...
A simple and efficient synthesis of 11<i>H</i>-pyrido[2,1-<i>b</i>]quinazolin-11-ones by Cu(OAc)<...
A variety of tetrahydro-5H-indolo[2,3-b]quinolines were prepared in 40–97% yields through a copper(I...
A simple and efficient synthesis of 11<i>H</i>-pyrido[2,1-<i>b</i>]quinazolin-11-ones by Cu(OAc)<...
Lately, the cross‐dehydrogenative coupling of tetrahydroisoquinolines and nitroalkanes has become a ...
The first highly enantioselective copper-catalyzed intramolecular Ullmann C–N coupling reaction has ...
The first highly enantioselective copper-catalyzed intramolecular Ullmann C–N coupling reaction has ...
International audienceA copper-catalyzed three-component assembly of cyanamides, 2-cyanoarylboronic ...
A convenient catalytic protocol for efficiently constructing indoline-fused tetrahydroisoquinolines ...
A convenient CuI/L-proline-catalyzed, two-step one-pot method has been developed for the preparation...
An efficient three-component domino reaction of 2-bromoaldehydes, benzylamines, and sodium azide has...
Highly selective and convenient synthesis of indolo[1,2-<i>c</i>]quinazolines and 11<i>H</i>-indol...
Herein, a copper(II)-catalyzed dearomative cyclization amination of N-(2-aminobenzoyl) indoles is pr...
A synthetic approach to quinindoline derivatives by the Cu-catalyzed dual cyclization has been devel...
A novel copper-catalyzed synthesis of quinazolinones from easily available 2-arylindoles and amines ...
[[abstract]]An efficient and novel procedure for a copper catalyzed domino coupling reaction has bee...
A simple and efficient synthesis of 11<i>H</i>-pyrido[2,1-<i>b</i>]quinazolin-11-ones by Cu(OAc)<...
A variety of tetrahydro-5H-indolo[2,3-b]quinolines were prepared in 40–97% yields through a copper(I...
A simple and efficient synthesis of 11<i>H</i>-pyrido[2,1-<i>b</i>]quinazolin-11-ones by Cu(OAc)<...
Lately, the cross‐dehydrogenative coupling of tetrahydroisoquinolines and nitroalkanes has become a ...
The first highly enantioselective copper-catalyzed intramolecular Ullmann C–N coupling reaction has ...
The first highly enantioselective copper-catalyzed intramolecular Ullmann C–N coupling reaction has ...
International audienceA copper-catalyzed three-component assembly of cyanamides, 2-cyanoarylboronic ...
A convenient catalytic protocol for efficiently constructing indoline-fused tetrahydroisoquinolines ...