The key steps of a versatile new protocol for the convergent synthesis of 3,4-disubstituted indoles are the addition of an α-lithiated alkylaminofuran to a carbonyl compound, a microwave-accelerated intramolecular Diels-Alder cycloaddition and an in situ double aromatization reaction. © The Royal Society of Chemistry
Heterocyclic products have been accomplished using microwave-assisted [Pd]-catalyzed intramolecular ...
A novel and efficient synthesis of phenanthridines and aza analogues is reported. The key step is a ...
The synthesis of [a]-annelated pyrazolopyrroloindoles via intramolecular 1,3-dipolar cycloaddition o...
The key steps of a versatile new protocol for the convergent synthesis of 3,4-disubstituted indoles ...
The first section of this thesis describes a novel allylic isomerization, followed by an intra-molec...
A convergent approach provides a convenient access to synthetically and biologically useful 3,4-disu...
none6noDue to the presence of the indole ring in a number of bioactive compounds, novel methods for ...
A novel highly efficient preparative method for the synthesis of substituted indoles using conjugate...
1-(Propargyl)indol-2-carbonitriles react with alcohols to afford 1-alkoxypyrazino[1,2-a]indoles unde...
The synthesis of the pyrazino[1,2-α]indole nucleus was achieved by intramolecular cyclization of sev...
As a part of our study directed to the development of intramolecular palladium-catalyzed procedure i...
The emergence of benzo[b]thiophenes and benzo[b]furans as biologically useful scaffolds is of growin...
1001-1005An efficient and clean procedure for the synthesis of a new hexacyclic system indeno-pyrano...
Intramolecular Diels Alder (IMDA) cycloaddition of the ester-tethered 1,3,9,-decatrienes possessing ...
An efficient and simplified protocol for uncatalyzed Friedel– Crafts alkylation of indoles using mic...
Heterocyclic products have been accomplished using microwave-assisted [Pd]-catalyzed intramolecular ...
A novel and efficient synthesis of phenanthridines and aza analogues is reported. The key step is a ...
The synthesis of [a]-annelated pyrazolopyrroloindoles via intramolecular 1,3-dipolar cycloaddition o...
The key steps of a versatile new protocol for the convergent synthesis of 3,4-disubstituted indoles ...
The first section of this thesis describes a novel allylic isomerization, followed by an intra-molec...
A convergent approach provides a convenient access to synthetically and biologically useful 3,4-disu...
none6noDue to the presence of the indole ring in a number of bioactive compounds, novel methods for ...
A novel highly efficient preparative method for the synthesis of substituted indoles using conjugate...
1-(Propargyl)indol-2-carbonitriles react with alcohols to afford 1-alkoxypyrazino[1,2-a]indoles unde...
The synthesis of the pyrazino[1,2-α]indole nucleus was achieved by intramolecular cyclization of sev...
As a part of our study directed to the development of intramolecular palladium-catalyzed procedure i...
The emergence of benzo[b]thiophenes and benzo[b]furans as biologically useful scaffolds is of growin...
1001-1005An efficient and clean procedure for the synthesis of a new hexacyclic system indeno-pyrano...
Intramolecular Diels Alder (IMDA) cycloaddition of the ester-tethered 1,3,9,-decatrienes possessing ...
An efficient and simplified protocol for uncatalyzed Friedel– Crafts alkylation of indoles using mic...
Heterocyclic products have been accomplished using microwave-assisted [Pd]-catalyzed intramolecular ...
A novel and efficient synthesis of phenanthridines and aza analogues is reported. The key step is a ...
The synthesis of [a]-annelated pyrazolopyrroloindoles via intramolecular 1,3-dipolar cycloaddition o...
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