A one-pot Barluenga coupling between N-tosylhydrazones and nitro-benzyl bromide, followed by deoxygenation of ortho-nitrostyrenes, and subsequent cyclization has been developed, providing a new way to synthesize various C2-arylindoles. This method exhibits a good substrate scope and functional group tolerance, and it allows an access to NH-free indoles, which can present a potential utility in medicinal chemistry applications
Brönsted acid-catalyzed one-pot synthesis of indoles from <i>o</i>-aminobenzyl alcohols and furans ...
An efficient route to substituted 1-aryl-1H-indazoles has been developed and optimized. The method i...
(Chemical Equation Presented) A single tandem operation allows rapid access to a variety of substitu...
International audienceA one-pot Barluenga coupling between N-tosylhydrazones and nitro-benzylbromide...
We report herein an original protocol to the indole nucleus, which could contribute to significantly...
2-Arylindoles are privileged structures widely present in biologically active molecules. New sustain...
A novel, sequential, palladium-catalyzed, cross-coupling reaction using <i>N</i>-tosylhydrazone and ...
This paper reports an one-pot method for the concomitant alkylation - oxidation (aromatization) of i...
The development of a long-term manufacturing route to a potent and selective KDR kinase inhibitor ha...
Palladium-phenanthroline complexes efficiently catalyze the reaction of nitroarenes with arylalkynes...
An efficient catalytic cyclization of \u3b2-nitrostyrenes to indoles was developed. The reaction was...
The thermal reaction between nitrosoarenes and alkynes under alkylating conditions produces N-alkoxy...
The selective construction of medicinally and synthetically important indole-based unsymmetrical tri...
Given the prevalence of molecules containing nitro groups in organic synthesis, innovative methods t...
A cyanide-free one-pot procedure was developed to access 2-amino-3-hydroxy-3<i>H</i>-indoles, which ...
Brönsted acid-catalyzed one-pot synthesis of indoles from <i>o</i>-aminobenzyl alcohols and furans ...
An efficient route to substituted 1-aryl-1H-indazoles has been developed and optimized. The method i...
(Chemical Equation Presented) A single tandem operation allows rapid access to a variety of substitu...
International audienceA one-pot Barluenga coupling between N-tosylhydrazones and nitro-benzylbromide...
We report herein an original protocol to the indole nucleus, which could contribute to significantly...
2-Arylindoles are privileged structures widely present in biologically active molecules. New sustain...
A novel, sequential, palladium-catalyzed, cross-coupling reaction using <i>N</i>-tosylhydrazone and ...
This paper reports an one-pot method for the concomitant alkylation - oxidation (aromatization) of i...
The development of a long-term manufacturing route to a potent and selective KDR kinase inhibitor ha...
Palladium-phenanthroline complexes efficiently catalyze the reaction of nitroarenes with arylalkynes...
An efficient catalytic cyclization of \u3b2-nitrostyrenes to indoles was developed. The reaction was...
The thermal reaction between nitrosoarenes and alkynes under alkylating conditions produces N-alkoxy...
The selective construction of medicinally and synthetically important indole-based unsymmetrical tri...
Given the prevalence of molecules containing nitro groups in organic synthesis, innovative methods t...
A cyanide-free one-pot procedure was developed to access 2-amino-3-hydroxy-3<i>H</i>-indoles, which ...
Brönsted acid-catalyzed one-pot synthesis of indoles from <i>o</i>-aminobenzyl alcohols and furans ...
An efficient route to substituted 1-aryl-1H-indazoles has been developed and optimized. The method i...
(Chemical Equation Presented) A single tandem operation allows rapid access to a variety of substitu...