Results 11 to 20 of about 30,747 (247)

Phosphorus pentasulfide mediated conversion of organic thiocyanates to thiols

open access: yesBeilstein Journal of Organic Chemistry, 2017
In this paper we report an efficient and mild procedure for the conversion of organic thiocyanates to thiols in the presence of phosphorus pentasulfide (P2S5) in refluxing toluene.
Chandra Kant Maurya   +2 more
doaj   +2 more sources

Sirtuin 1 Inhibiting Thiocyanates (S1th)—A New Class of Isotype Selective Inhibitors of NAD+ Dependent Lysine Deacetylases

open access: yesFrontiers in Oncology, 2020
Sirtuin 1 (Sirt1) is a NAD+ dependent lysine deacetylase associated with the pathogenesis of various diseases including cancer. In many cancer types Sirt1 expression is increased and higher levels have been associated with metastasis and poor prognosis ...
Nathalie Wössner   +11 more
doaj   +2 more sources

Inorganic Metal Thiocyanates

open access: yesInorganic Chemistry
Metal thiocyanates were some of the first pseudohalide compounds to be discovered and adopt a diverse range of structures. This review describes the structures, properties, and syntheses of the known binary and ternary metal thiocyanates. It provides a categorization of their diverse structures and connects them to the structures of atomic inorganic ...
M. Cliffe
openaire   +3 more sources

Strengthening the Magnetic Interactions in Pseudobinary First-Row Transition Metal Thiocyanates, M(NCS)2. [PDF]

open access: yesInorganic Chemistry, 2020
Understanding the effect of chemical composition on the strength of magnetic interactions is key to the design of magnets with high operating temperatures.
Euan N. Bassey   +8 more
semanticscholar   +1 more source

Straightforward Access to Thiocyanates via Dealkylative Cyanation of Sulfoxides

open access: yesOrganic Letters, 2021
Thiocyanates, versatile building blocks in organic synthesis, are shown to be easily accessible via an interrupted Pummerer reaction of sulfoxides. This facile dealkylative functionalization proceeds under mild conditions through electrophilic activation
U. Todorović, Immo Klose, N. Maulide
semanticscholar   +1 more source

Electrosynthesis of ( E)-Vinyl Thiocyanates from Cinnamic Acids via Decarboxylative Coupling Reaction.

open access: yesOrganic Letters, 2019
Thiocyanate compounds are key intermediates in the synthesis of pharmaceuticals and other sulfur-containing organic compounds. Herein, we first report an electrochemical protocol to synthesize vinyl thiocyanates from decarboxylative coupling of cinnamic ...
Shun Yang   +3 more
semanticscholar   +1 more source

Remote functionalization by tandem radical chain reactions [PDF]

open access: yes, 1997
Normal radical relay chlorination of cholestan-3α-ol directed by an attached m-iodobenzoate ester group affords a 9α-chloro steroid, but when the same reaction is conducted in the presence of an excess of CBr4 the product is a 9α-bromo steroid ...
Wiedenfeld, David
core   +1 more source

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

Constructing chiral MOFs by functionalizing 4,2′:6′,4″-terpyridine with long-chain alkoxy domains: rare examples of neb nets [PDF]

open access: yes, 2016
Reactions of 4′-(4- n alkyloxyphenyl)-4,2′:6′,4″-terpyridines (alkyl = hexyl or nonyl) with CoIJNCS) 2 lead to three structurally characterized chiral 3D assemblies which adopt rare neb topologies.
Coles, Simon   +5 more
core   +1 more source

LEAD THIOCYANATE. [PDF]

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

Home - About - Disclaimer - Privacy