3-Carbamoylmethyl-Indole-1-Carboxylic Acid Ethyl Ester (an ethoxycarbonyl derivative of indole-3-acetamide) is obtained by Friedel–Crafts type cyclocondensation of γ-functionalized acetoacetamide in neat polyphosphoric acid
The p-TsOH-catalyzed Diels–Alder reaction of 3-(indol-3-yl)maleimides with chalcone in toluene at 60...
The title compound, C14H17NO3, having an ethoxycarbonyl group at C2, serves as an important precurso...
Triethylamine-mediated carboxymethylation of ethyl cellulose using monochloroacetic acid produced a ...
2421-24241-Oxo-1,2,3,4-tetrahydrocarbazoles 1a-e and 1-oxo-1,2 ,3,4,5,10- hexahydrocyclohept[b] ind...
A highly efficient one-pot method for the reductive coupling of indoles to nitrostyrenes in polyphos...
<div><p></p><p>Friedel–Crafts reaction of indoles to aromatic α-ketimino esters was found to be cata...
A number of trifluoromethylated 3-(pyrazolyl)indoles was synthesized from 2-(trifluoromethyl)comanic...
The synthesis of the indolo[2,3-a]carbazole ring is described starting from 3-chloromethylene-1,3-di...
A simple and flexible approach to 3-pyrrolin-2-one fused carbazoles is disclosed. The key step invol...
The reaction of ethyl 3-(o-trifluoroacetamidoaryl)-1-propargylic esters with ethyl iodoacetate or α-...
Successful alkylations of the nitrogen of ethyl indol-2-carboxylate were carried out using aq. KOH i...
The intramolecular Friedel-Crafts reaction of indole-2-carboxylic acid \u3b2-oxoamides catalyzed by ...
Acid treatment of indole-2-carboxylic acid b- and g-oxoamides causes Friedel–Crafts intramolecular c...
Simple synthetic approaches to pyridocarbazole and azepinocarbazole derivatives have been reported v...
The title compound, C14H17NO3, having an ethoxy-carbonyl group at C2, serves as an important precurs...
The p-TsOH-catalyzed Diels–Alder reaction of 3-(indol-3-yl)maleimides with chalcone in toluene at 60...
The title compound, C14H17NO3, having an ethoxycarbonyl group at C2, serves as an important precurso...
Triethylamine-mediated carboxymethylation of ethyl cellulose using monochloroacetic acid produced a ...
2421-24241-Oxo-1,2,3,4-tetrahydrocarbazoles 1a-e and 1-oxo-1,2 ,3,4,5,10- hexahydrocyclohept[b] ind...
A highly efficient one-pot method for the reductive coupling of indoles to nitrostyrenes in polyphos...
<div><p></p><p>Friedel–Crafts reaction of indoles to aromatic α-ketimino esters was found to be cata...
A number of trifluoromethylated 3-(pyrazolyl)indoles was synthesized from 2-(trifluoromethyl)comanic...
The synthesis of the indolo[2,3-a]carbazole ring is described starting from 3-chloromethylene-1,3-di...
A simple and flexible approach to 3-pyrrolin-2-one fused carbazoles is disclosed. The key step invol...
The reaction of ethyl 3-(o-trifluoroacetamidoaryl)-1-propargylic esters with ethyl iodoacetate or α-...
Successful alkylations of the nitrogen of ethyl indol-2-carboxylate were carried out using aq. KOH i...
The intramolecular Friedel-Crafts reaction of indole-2-carboxylic acid \u3b2-oxoamides catalyzed by ...
Acid treatment of indole-2-carboxylic acid b- and g-oxoamides causes Friedel–Crafts intramolecular c...
Simple synthetic approaches to pyridocarbazole and azepinocarbazole derivatives have been reported v...
The title compound, C14H17NO3, having an ethoxy-carbonyl group at C2, serves as an important precurs...
The p-TsOH-catalyzed Diels–Alder reaction of 3-(indol-3-yl)maleimides with chalcone in toluene at 60...
The title compound, C14H17NO3, having an ethoxycarbonyl group at C2, serves as an important precurso...
Triethylamine-mediated carboxymethylation of ethyl cellulose using monochloroacetic acid produced a ...
DOI
Add to ORKG