The direct thiocyanation of indoles and pyrrole with ammonium thiocyanate has been achieved using o-iodoxybenzoic acid (IBX) under mild and neutral conditions to produce indol-3-yl and pyrrol-2-yl thiocyanates, respectively, in excellent yields and with high selectivity. This method is effective even with N-substituted arylamines for the preparation of aryl thiocyanates
The cyanation of organic compounds is an important and useful process as it directly provides nitril...
An efficient and general rhodium(III) catalyzed C2-selective cyanation of indoles and pyrroles was ...
An efficient GaCl3-catalyzed direct cyanation of indoles and pyrroles using bench-stable electrophil...
Selectfluor<SUP>TM</SUP> is found to catalyze efficiently the electrophilic thiocyanation of indoles...
Indoles, pyrroles, oxindoles and aromatic amino compounds undergo smooth thiocyanation with ammonium...
BF3 center dot OEt2-catalyzed direct cyanation of indoles and pyrroles using a less toxic, bench-sta...
<p>An efficient and simple method is reported for the cyanation on arylboronic acid using various si...
Indoles, oxindoles and aromatic amino compounds undergo smooth thiocyanation with ammonium thiocyana...
Indoles and azaindoles undergo smooth oxidation with 2-iodoxybenzoic acid (IBX) in the presence of i...
Oxidative potential of trans3,5dihydroperoxy3,5dimethyl1,2dioxolane (DHPODMDO) has been explored in ...
<div><p>A green and regioselective thiocyanation of aromatic and heteroaromatic compounds has been a...
The one-step synthesis of the bench-stable hypervalent iodine reagents IndoleBX and PyrroleBX using ...
Copper-mediated regioselective cyanation of indoles and 2-phenylpyridines was developed by using amm...
A highly efficient approach to 2,3-disubstituted indoles has been presented. The indole precursors, ...
Organic chemistry is essential for the development of a modern society and technical progress requir...
The cyanation of organic compounds is an important and useful process as it directly provides nitril...
An efficient and general rhodium(III) catalyzed C2-selective cyanation of indoles and pyrroles was ...
An efficient GaCl3-catalyzed direct cyanation of indoles and pyrroles using bench-stable electrophil...
Selectfluor<SUP>TM</SUP> is found to catalyze efficiently the electrophilic thiocyanation of indoles...
Indoles, pyrroles, oxindoles and aromatic amino compounds undergo smooth thiocyanation with ammonium...
BF3 center dot OEt2-catalyzed direct cyanation of indoles and pyrroles using a less toxic, bench-sta...
<p>An efficient and simple method is reported for the cyanation on arylboronic acid using various si...
Indoles, oxindoles and aromatic amino compounds undergo smooth thiocyanation with ammonium thiocyana...
Indoles and azaindoles undergo smooth oxidation with 2-iodoxybenzoic acid (IBX) in the presence of i...
Oxidative potential of trans3,5dihydroperoxy3,5dimethyl1,2dioxolane (DHPODMDO) has been explored in ...
<div><p>A green and regioselective thiocyanation of aromatic and heteroaromatic compounds has been a...
The one-step synthesis of the bench-stable hypervalent iodine reagents IndoleBX and PyrroleBX using ...
Copper-mediated regioselective cyanation of indoles and 2-phenylpyridines was developed by using amm...
A highly efficient approach to 2,3-disubstituted indoles has been presented. The indole precursors, ...
Organic chemistry is essential for the development of a modern society and technical progress requir...
The cyanation of organic compounds is an important and useful process as it directly provides nitril...
An efficient and general rhodium(III) catalyzed C2-selective cyanation of indoles and pyrroles was ...
An efficient GaCl3-catalyzed direct cyanation of indoles and pyrroles using bench-stable electrophil...