Results 51 to 60 of about 20,785 (192)

Copper-Catalyzed Regioselective Synthesis of (E)-β-Fluorovinyl Sulfones

open access: yesMolecules, 2019
Organofluorine compounds are finding increasing application in a variety of fields such as pharmaceutical, agrochemical, and material sciences. However, given the scarcity of fluorine-containing natural products, advancement in this area depends almost ...
Raquel Román   +4 more
doaj   +1 more source

Synthesis of Alkyl Aryl Sulfones via Reaction of N-Arylsulfonyl Hydroxyamines with Electron-Deficient Alkenes

open access: yesMolecules, 2016
Alkyl aryl sulfones were prepared in high yields via the reaction of N-arylsulfonyl hydroxylamines with electron-deficient alkenes. These reactions have the advantages of simplicity, easily available starting materials and mild reaction conditions.
Yunhui Bin, Ruimao Hua
doaj   +1 more source

Thermoplastic polyether sulfones for composite materials reinforced with fabrics [PDF]

open access: diamond, 2021
I P Storoshuk   +5 more
openalex   +1 more source

Antimalarial effects of vinyl sulfone cysteine proteinase inhibitors [PDF]

open access: bronze, 1996
Philip J. Rosenthal   +5 more
openalex   +1 more source

Surface Nanosieving Polyether Sulfone Particles with\nGraphene Oxide Encapsulation for the Negative Isolation toward Extracellular\nVesicles

open access: green, 2021
Yilan Li (737146)   +8 more
openalex   +2 more sources

Synthesis of Adenine Nucleosides with a Reactive (β-Iodovinyl)sulfone or (β-Keto)sulfone Group at the C2 Position and Their Polymerase-Catalyzed Incorporation into DNA

open access: yesMolecules
Iodosulfonylation of an ethynyl group at the C2 position of 2′-deoxyadenosine or adenosine with TsI provides (E)-2-(β-iodovinyl)sulfones. The latter undergo nucleophilic substitution with amines via an addition–elimination to give β-sulfonylvinylamines ...
A. Hasan Howlader   +4 more
doaj   +1 more source

sulfones

open access: yes, 2014
Citation: 'sulfones' in the IUPAC Compendium of Chemical Terminology, 3rd ed.; International Union of Pure and Applied Chemistry; 2006. Online version 3.0.1, 2019. 10.1351/goldbook.S06117 • License: The IUPAC Gold Book is licensed under Creative Commons Attribution-ShareAlike CC BY-SA 4.0 International for individual terms.
openaire   +1 more source

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