Results 161 to 170 of about 7,973 (208)

Degradable N-Vinyl Copolymers through Radical Ring-Opening Polymerization of Cyclic Thionocarbamates. [PDF]

ACS Macro Lett
Calderón-Díaz A, Boggiano AC, Xiong W, Kaiser N, Gutekunst WR.   +4 more
europepmc   +1 more source

2,5-Diazabicyclo[2.2.1]heptane in medicinal chemistry: a treasure trove of therapeutic opportunities. [PDF]

RSC Med Chem
Ambast PK, Kapoor S, Das R, Chatterjee DR, Shard A.   +4 more
europepmc   +1 more source

Metal-free site-selective functionalization with cyclic diaryl λ³-chloranes: suppression of benzyne formation for ligand-coupling reactions. [PDF]

Chem Sci
Patra K, Dey MP, Baidya M.
europepmc   +1 more source

Exploring the Reactivity of Electrophilic Organic Carbonates and Thiocarbonates as Vehicles to Convert Hydrosulfide into COS and CS₂. [PDF]

J Org Chem
Wade Wolfe MM, Pines JE, Sosa AR, Pluth MD.   +3 more
europepmc   +1 more source

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Insight into stability of dithiocarbamate-modified adsorbents: Oxidation of dithiocarbamate

Chemosphere, 2023
We previously reported that monoalkyl dithiocarbamate-modified cellulose (DMC) exhibited excellent adsorption performance for arsenite (AsIII), cadmium (CdII), lead (PbII), gold (AuIII), silver (AgI), platinum (PtIV), and palladium (PdII). However, its adsorption capability for AsIII decreased by 96.4% after two weeks of storage at 40 °C under an air ...
Keisuke Nakakubo, Foni B. Biswas, Tsuyoshi Taniguchi, Masaru Endo, Yuto Sakai, Kuo H. Wong, Asami S. Mashio, Tatsuya Nishimura, Katsuhiro Maeda, Hiroshi Hasegawa   +9 more
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Rearrangement of cyclic dithiocarbamates

Chemistry of Heterocyclic Compounds, 2006
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
T. P. Trofimova, A. N. Pushin, Ya. I. Lys, V. M. Fedoseev   +3 more
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Antiradiation Compounds. II. Dithiocarbamates

Journal of Medicinal and Pharmaceutical Chemistry, 1962
Substituted dithiocarbamic acid derivatives, some of which contain metal- chelating functions additional to the dithiocarbamyl group, were synthesized as potential protective agents against ionizing radiation. It appeared that the additional nitrogen-containing chelating function contributed nothing to the radioprotective ability of dithiocarbamates ...
W O, FOYE, J, MICKLES
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Pesticide Residues: Dithiocarbamates

2014
Dithiocarbamates are synthetic organic compounds containing sulfur and often a sulfur-bound metal, some of which are used to protect fruits and vegetables from fungal infections. Exposure of the general population results from occasional residues in foodstuff.
F. Rubino, E. Mrema, C. Colosio
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