Add to ORKGThe reaction of isatin and indoles in refluxing water/ethanol (7:3) affords 3,3'-di(indolyl)oxindoles in excellent yields
Indole-2-one derivatives were prepared from the corrisponding isatines via one pot reduction in hydr...
An "on water" organocatalytic cyanoarylmethylation of aryl acetonitrile to isatins is developed, giv...
Isatins are synthetically versatile substrates, where they can be used for the synthesis of a large ...
The reaction of isatin and indoles in refluxing water/ethanol (7:3) affords 3,3'- di(indolyl)oxindo...
A condensation of various isatins with indole derivatives has been carried out in the presence of 1,...
An expeditious, functional group-tolerant synthesis of indoles from isatins is described. Isatins ar...
A condensation of various isatins with indole derivatives has been carried out in the presence of 1,...
An easy protocol for the synthesis of enaminone attached 3-substituted-3-hydroxy-2-oxindoles has bee...
Indoles and azaindoles undergo smooth oxidation with 2-iodoxybenzoic acid (IBX) in the presence of i...
<p>A greener approach for the synthesis of 4-oxo-4,5,6,7-tetrahydro indole derivatives has been achi...
<p>An efficient and greener protocol for easy access to 3-susbstituted-3-hydroxy-2-oxindoles by the ...
An "on water" organocatalytic cyanoarylmethylation of aryl acetonitrile to isatins is developed, giv...
Isatins undergo efficient allylation/propargylation when reacted with allyl/propargyl bromide in the...
Indole-2-one derivatives were prepared from the corrisponding isatines via one pot reduction in hydr...
Indole-2-one derivatives were prepared from the corrisponding isatines via one pot reduction in hydr...
Indole-2-one derivatives were prepared from the corrisponding isatines via one pot reduction in hydr...
An "on water" organocatalytic cyanoarylmethylation of aryl acetonitrile to isatins is developed, giv...
Isatins are synthetically versatile substrates, where they can be used for the synthesis of a large ...
The reaction of isatin and indoles in refluxing water/ethanol (7:3) affords 3,3'- di(indolyl)oxindo...
A condensation of various isatins with indole derivatives has been carried out in the presence of 1,...
An expeditious, functional group-tolerant synthesis of indoles from isatins is described. Isatins ar...
A condensation of various isatins with indole derivatives has been carried out in the presence of 1,...
An easy protocol for the synthesis of enaminone attached 3-substituted-3-hydroxy-2-oxindoles has bee...
Indoles and azaindoles undergo smooth oxidation with 2-iodoxybenzoic acid (IBX) in the presence of i...
<p>A greener approach for the synthesis of 4-oxo-4,5,6,7-tetrahydro indole derivatives has been achi...
<p>An efficient and greener protocol for easy access to 3-susbstituted-3-hydroxy-2-oxindoles by the ...
An "on water" organocatalytic cyanoarylmethylation of aryl acetonitrile to isatins is developed, giv...
Isatins undergo efficient allylation/propargylation when reacted with allyl/propargyl bromide in the...
Indole-2-one derivatives were prepared from the corrisponding isatines via one pot reduction in hydr...
Indole-2-one derivatives were prepared from the corrisponding isatines via one pot reduction in hydr...
Indole-2-one derivatives were prepared from the corrisponding isatines via one pot reduction in hydr...
An "on water" organocatalytic cyanoarylmethylation of aryl acetonitrile to isatins is developed, giv...
Isatins are synthetically versatile substrates, where they can be used for the synthesis of a large ...