Results 31 to 40 of about 3,977 (192)

Near‐Infrared‐Light‐Driven Photochemistry and Photocatalysis: Mechanisms, Recent Applications, and Opportunities in Organic Synthesis and Biology

open access: yesAngewandte Chemie, EarlyView.
This minireview highlights recent advances in catalyst development and mechanistic strategies that enable photochemical and photocatalytic reactivity under 700–1000 nm NIR light, emphasizing how long‐wavelength excitation expands opportunities in both synthetic chemistry and biology.
Santosh K. Pagire   +3 more
wiley   +2 more sources

Click grafting of seaweed polysaccharides onto PVC surfaces using an ionic liquid as solvent and catalyst [PDF]

open access: yes, 2013
International audienceSeaweed antibacterial polysaccharides were grafted onto poly(vinylchloride) (PVC) surfaces using an original click chemistry pathway.
Bigot, Sandra,   +3 more
core   +4 more sources

Unprecedented spin localisation in a metal-metal bonded dirhenium complex [PDF]

open access: yes, 2015
he molecular and electronic structure of edge-sharing bioctahedral [N(n-Bu)4]3[Re2(mnt)5] is reported here. Despite the short intermetal bond length of 2.6654(2) Å with computed bond order of 1.2, the unpaired electron is localised by the asymmetric ...
Donahue, James   +3 more
core   +1 more source

Biological Evaluation and Docking Studies of New Carbamate, Thiocarbamate, and Hydrazide Analogues of Acyl Homoserine Lactones as Vibrio fischeri-Quorum Sensing Modulators

open access: yesBiomolecules, 2020
A series of carbamate, thiocarbamate, and hydrazide analogues of acylhomoserine lactones (AHLs) were synthesized and their ability to modulate Vibrio fischeri-quorum sensing was evaluated.
Qiang Zhang   +2 more
doaj   +1 more source

Crystal structure of the (E)-O-methyl-N-phenyl-thiocarbamate – 4,4′-bipyridine (1/1), C18H17N3OS [PDF]

open access: yes, 2018
C18H17N3OS, monoclinic, C2/c (no. 15), a=13.4754(3) Å, b=13.8997(3) Å, c=18.0300(4) Å, β=107.202(3)°, V =3226.03(13) Å3, Z =8, Rgt(F)=0.0341, wRref(F2)=0.0878, T =100(2 ...
Tiekink, Edward R. T. *   +1 more
core   +1 more source

A monoclinic polymorph of [(Z)-N-(3-chlorophenyl)-O-methylthiocarbamato-κS](triphenylphosphane-κP)gold(I): crystal structure and Hirshfeld surface analysis

open access: yesActa Crystallographica Section E: Crystallographic Communications, 2016
The title compound, [Au(C8H7ClNOS)(C18H15P)], is a monoclinic (P21/n, Z′ = 1; form β) polymorph of the previously reported triclinic form (P-1, Z′ = 1; form α) [Tadbuppa & Tiekink (2010). Acta Cryst. E66, m664].
Chien Ing Yeo   +2 more
doaj   +1 more source

Characterization of the nucleophilic reactivities of thiocarboxylate, dithiocarbonate and dithiocarbamate anions [PDF]

open access: yes, 2011
The kinetics of the reactions of thiocarboxylate and thiocarbonate anions with benzhydrylium ions have been determined in acetonitrile solution using laser-flash photolytic techniques.
Duan, Xin-Hua   +2 more
core   +1 more source

Crystal structure of 4-{[(cyanoimino)(methylsulfanyl)methyl]amino}-1,5-dimethyl-2-phenyl-2,3-dihydro-1H-pyrazol-3-one

open access: yesActa Crystallographica Section E: Crystallographic Communications, 2015
In the title compound, C14H15N5OS, the tautomer present in the solid state is that in which the immediately exocyclic N atom bears the H atom. The central five-membered ring is almost planar (r.m.s.
Galal H. Elgemeie   +2 more
doaj   +1 more source

Synthesis and pre-clinical evaluation of a [18F] fluoromethyl-tanaproget derivative for imaging of progesterone receptor expression [PDF]

open access: yes, 2016
The estrogen receptor (ER) and progesterone receptor (PR) are over-expressed in ∼50% of breast cancer lesions, and used as biomarkers to stratify patients for endocrine therapy. Currently, immunohistochemical (IHC) assessment of these lesions from a core-
Aboagye, EO   +8 more
core   +1 more source

Synthesis of Secondary Amides from Thiocarbamates [PDF]

open access: yesOrganic Letters, 2018
The synthesis of secondary amides from readily accessible and bench-stable substituted S-phenyl thiocarbamates and Grignard reactants is reported. Oxidative workup allows recycling of the thiolate leaving group as diphenyl disulfide. Diphenyl disulfide can be transformed into S-phenyl benzenethiosulfonate, a reactant required for thiocarbamate ...
Pieter Mampuys   +3 more
openaire   +2 more sources

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