Results 61 to 70 of about 319 (90)

1-Chloromethyl-4-fluoro-1,4-diazoniabicyclo[2,2,2]octane bis(tetrafluoroborate) as novel and versatile reagent for the rapid thiocyanation of indoles, azaindole, and carbazole

open access: yes, 2008
SelectfluorTM is found to catalyze efficiently the electrophilic thiocyanation of indoles and pyrrole with ammonium thiocyanate under mild and neutral conditions to produce the corresponding 3-indolyl and 2-pyrrolyl thiocyanates, respectively, in ...
Jayasudhan Reddy, Y.   +2 more
core   +1 more source

Thiocyanation of BODIPY dyes and their conversion to thioalkylated derivatives

open access: yes, 2015
A high-yielding method for the direct thiocyanation of BODIPY dyes is described. In 1,3-dimethyl BODIPYs, the thiocyanato group adds at position 2, whereas the insertion occurs at position 5 in 3-amino BODIPYs. The transformation of the thiocyanato group
Verbelen, Bram   +5 more
core   +1 more source

Efficient Oxidative Dehydrogenation of Dihydropyrimidinones and Thiocyanation of Aromatic Compounds Using 1,1,2,2-Tetrahydroperoxy-1,2-diphenylethane as the Oxidant

open access: yes, 2019
A new, efficient and mild approach for the oxidative dehydrogenation of dihydropyrimidinones and thiocyanation of aromatic compounds using 1,1,2,2-tetrahydroperoxy-1,2-diphenylethane (THPDPE) as a terminal oxidant was developed.
Naserifar, Shirin   +5 more
core   +1 more source

Ring-Opening Thiocyanation Reaction of Sulfonium Salts with Elemental Sulfur and TMSCN

open access: yes
A simple and efficient strategy has been developed for the synthesis of organic thiocyanates through direct ring-opening thiocyanation reactions of aryl, alkenyl, and alkynyl sulfonium ylides using elemental sulfur and TMSCN.
Linghao Ran   +7 more
core   +1 more source

1-Methyl-3-(2-(Sulfooxy)Ethyl)-1H-Imidazol-3-Ium Thiocyanate as A Novel, Green, and Efficient BrØNsted Acidic Ionic Liquid-Promoted Regioselective Thiocyanation of Aromatic and Heteroaromatic Compounds at Room Temperature

open access: yes, 2014
An efficient and simple method for the preparation of 1-methyl-3-(2-(sulfooxy)ethyl)-1H-imidazol-3-ium thiocyanate ([Msei]SCN)as a Brønsted acidic ionic liquid (BAIL) is described, and it is used in the highly efficient regioselective ...
Eshagh Rezaee Nezhad (536804)   +4 more
core   +1 more source

Thiocyanation of 3-substituted and 3,5-disubstituted BODIPYs and its application for the synthesis of new fluorescent sensors

open access: yes, 2018
© 2018 Elsevier Ltd Interest in BODIPYs (acronym of boron dipyrromethene) has skyrocketed in recent decades, mainly due to their favourable photophysical properties and the wide range of functionalization methods reported for these organic fluorescent ...
Verbelen, Bram   +5 more
core   +1 more source

Thiocyanation of closo-Dodecaborate B12H122−. A Novel Synthetic Route and Theoretical Elucidation of the Reaction Mechanism

open access: yes, 2016
Although vast experimental experience has been accumulated about the reactions of icosahedral B12H122− borane cages, little is known about the mechanisms by which these reactions proceed. To address this issue, we have chosen the thiocyanation of B12H122−
Martin Lepšík (1265016)   +7 more
core   +1 more source

Mechanochemical Thiocyanation of Aryl Compounds via C–H Functionalization

open access: yesACS Omega, 2020
Edson de Oliveira Lima Filho   +1 more
doaj   +1 more source

Photocatalytic C–H Thiocyanation of NH2‑Enaminones and the Tunable Synthetic Routes to 2‑Aminothiazoles and 2‑Thiazolinones

open access: yes
Visible light photocatalytic reactions of NH2-enaminones and ammonium thiocyanate for chemoselective α-C–H thiocyanation have been realized for the first time, providing a sustainable route for the synthesis of thiocyanated NH2-enaminones.
Jie-Ping Wan (1393846)   +2 more
core   +1 more source

Iron‐Catalyzed Thiocyanation of Heterocycles and Aromatics Utilizing a Combination of NH 3 ·H 2 O and CS 2

open access: yes
In this study, we report the iron‐catalyzed thiocyanation of heterocycles and aromatics using NH 3 ·H 2 O and CS 2 as the SCN source ...
Yin‐Long Lai   +8 more
core   +1 more source

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