Results 21 to 30 of about 470 (176)

Organocatalyzed Asymmetric α‑Thiocyanation of Oxindoles: Synthesis of Chiral Tertiary 3‑Thiocyanatoxindoles

open access: yes, 2019
An enantioselective thiocyanation of oxindoles has been developed for the first time using a bifunctional cinchona-derived organo-catalyst and N-thiocyanatophthalimide as the electrophilic thiocyanation source in the presence of 2-naphthol as the ...
Fu-Xue Chen (2397511)   +5 more
core   +3 more sources

Recent Advances in Intramolecular C─N Bond Formation for Pyrrolidine Synthesis. [PDF]

open access: yesChemistryOpen
This review highlights synthetic advances (2013–2025) in intramolecular C─N bond formation for constructing the pharmaceutically relevant pyrrolidine core. The review is organized into five methodological clusters: 1) intramolecular alkene/alkyne amination; 2) tandem annulations, which involve C─N bond formation as the key step; 3) nucleophilic ...
Kroņkalne R, Turks M.
europepmc   +2 more sources

The Effect of Thiocyanate Concentration on Thiocyanate Distribution and Excretion

open access: yesExperimental Biology and Medicine, 1971
SummaryIt has been observed in rats that the measured volume of distribution of thiocyanate is decreased by high plasma concentrations of thiocyanate, and that large doses of thiocyanate have a faster rate of disappearance from the plasma than does endogenous thiocyanate at normal concentrations. These observations are interpreted as results of (i) the
C F, Funderburk, L, Van Middlesworth
openaire   +2 more sources

Water Microdroplet Chemistry for Accelerating Green Thiocyanation and Discovering Water-Controlled Divergence

open access: yes, 2023
As an important class of five-membered N-heterocyclic compounds, pyrazolin-5-one derivatives play an extremely important role in the construction of fine chemicals and bioactive molecules.
Luyun Xue   +9 more
core   +1 more source

LEAD THIOCYANATE. [PDF]

open access: yesJournal of the American Chemical Society, 1902
n ...
openaire   +2 more sources

Diquat Based Dyes: A New Class of Photoredox Catalysts and Their Use in Aerobic Thiocyanation [PDF]

open access: yes, 2023
A series of new organic donor-π-acceptor dyes incorporating a diquat moiety as a novel electron-acceptor unit have been synthesized and characterized. The analytical data were supported by DFT calculations.
Wilhelm, René   +9 more
core   +1 more source

Preparation of Arylthiocyanates Using N,N′-Dibromo-N,N′-bis(2,5-dimethylbenzenesulphonyl) ethylenediamine and N,NDibromo-2,5-dimethylbenzenesulphonamide in the Presence of KSCN as a Novel Thiocyanating Reagent

open access: yesMolecules, 2001
N-Bromosulphonamides, synthesized via direct bromination of sulphonamides, react with several types of arene substrates in the presence of KSCN to afford aryl thiocyanates. The method appears to be generally applicable to benzenoid substrates with a wide
Ardeshir Khazaei   +2 more
doaj   +1 more source

Mechanochemical Approach for Metal-Free Regioselective C5-Sulfenylation of Imidazo[2,1-b]Thiazoles. [PDF]

open access: yesChemSusChem
This study presents a mechanochemical approach for the metal‐free, regioselective C5‐sulfenylation of imidazo[2,1‐b]thiazoles using bis(trifluoroacetoxy)iodo]benzene and aryl methyl sulfides. The method, performed under solvent‐free ball‐milling conditions, provides an efficient, environmentally friendly alternative to conventional synthesis, achieving
Liu X   +6 more
europepmc   +2 more sources

Recent Advances in the Application of SelectfluorTMF-TEDA-BF4 as a Versatile Mediator or Catalyst in Organic Synthesis

open access: yesMolecules, 2011
SelectfluorTM F-TEDA-BF4 (1-chloromethyl-4-fluoro-1,4-diazoniabicyclo [2.2.2]octane bis(tetrafluoroborate) is not only one of the most efficient and popular reagents for electrophilic fluorination, but as a strong oxidant is also a convenient mediator or
Stojan Stavber
doaj   +1 more source

THE SYSTEMATIC DETECTION OF THIOCYANATES. [PDF]

open access: yesJournal of the American Chemical Society, 1916
n ...
Curtman, Louis J., Harris, Ben R.
openaire   +1 more source

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