Reaction of anodically generated thiocyanogen (NaSCN, LiClO4, MeCN, Pt, 0.9V vs SCE) with 3-alkylsubstituted indoles results preferentially in isothiocyanation at the indole 2-position rather than in the expected thiocyanation
The addition of carbon (Grignard and organolithium reagents) and hydride nucleophiles (Schwartz reag...
Heteroaryl, benzyl, and cinnamyl thiocyanates undergo smooth allylation with allyl bromide in the pr...
The reaction mechanism of the Pd(0)-catalyzed alkyne cyanothiolation reaction is investigated by MP2...
Indoles, pyrroles, oxindoles and aromatic amino compounds undergo smooth thiocyanation with ammonium...
A highly efficient approach to 2,3-disubstituted indoles has been presented. The indole precursors, ...
Indoles, oxindoles and aromatic amino compounds undergo smooth thiocyanation with ammonium thiocyana...
Selectfluor<SUP>TM</SUP> is found to catalyze efficiently the electrophilic thiocyanation of indoles...
International audienceThe synthesis of bench-stable electrophilic thiocyanating reagents was depicte...
An unprecedented transfer of a thiocyanate (−SCN) group from aroyl/acyl isothiocyanate to alkyl or b...
<p>Practical synthesis of 1,3-diaryl-substituted 3-isothiocyanatopropan-1-ones based on the reaction...
Oxidative potential of trans3,5dihydroperoxy3,5dimethyl1,2dioxolane (DHPODMDO) has been explored in ...
A number of tetraorganotin compounds of the types (CH3)3SnR and, to a lesser extent, (C6H5)3SnR, whe...
Indoles undergo smooth cyanation with CuCN in the presence of 20 mol % Pd(OAc)2 and 40 mol % CuBr2 i...
The cyanation of organic compounds is an important and useful process as it directly provides nitril...
Isothiocyanates (ITCs) are biologically active molecules found in several natural products and pharm...
The addition of carbon (Grignard and organolithium reagents) and hydride nucleophiles (Schwartz reag...
Heteroaryl, benzyl, and cinnamyl thiocyanates undergo smooth allylation with allyl bromide in the pr...
The reaction mechanism of the Pd(0)-catalyzed alkyne cyanothiolation reaction is investigated by MP2...
Indoles, pyrroles, oxindoles and aromatic amino compounds undergo smooth thiocyanation with ammonium...
A highly efficient approach to 2,3-disubstituted indoles has been presented. The indole precursors, ...
Indoles, oxindoles and aromatic amino compounds undergo smooth thiocyanation with ammonium thiocyana...
Selectfluor<SUP>TM</SUP> is found to catalyze efficiently the electrophilic thiocyanation of indoles...
International audienceThe synthesis of bench-stable electrophilic thiocyanating reagents was depicte...
An unprecedented transfer of a thiocyanate (−SCN) group from aroyl/acyl isothiocyanate to alkyl or b...
<p>Practical synthesis of 1,3-diaryl-substituted 3-isothiocyanatopropan-1-ones based on the reaction...
Oxidative potential of trans3,5dihydroperoxy3,5dimethyl1,2dioxolane (DHPODMDO) has been explored in ...
A number of tetraorganotin compounds of the types (CH3)3SnR and, to a lesser extent, (C6H5)3SnR, whe...
Indoles undergo smooth cyanation with CuCN in the presence of 20 mol % Pd(OAc)2 and 40 mol % CuBr2 i...
The cyanation of organic compounds is an important and useful process as it directly provides nitril...
Isothiocyanates (ITCs) are biologically active molecules found in several natural products and pharm...
The addition of carbon (Grignard and organolithium reagents) and hydride nucleophiles (Schwartz reag...
Heteroaryl, benzyl, and cinnamyl thiocyanates undergo smooth allylation with allyl bromide in the pr...
The reaction mechanism of the Pd(0)-catalyzed alkyne cyanothiolation reaction is investigated by MP2...
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