Results 1 to 10 of about 12,336 (293)

A reagent to access methyl sulfones [PDF]

open access: yesNature Communications
A chemical reagent to access methyl sulfones has been developed. Its reaction with various bis-nucleophiles leads to the rapid formation of previously unknown heteroaromatic methyl sulfones. Analogous strategy can also be used to construct alkyl-, CHF2-,
Yaroslav Poplavskyi   +11 more
doaj   +3 more sources

Hydrogenation of β-Keto Sulfones to β-Hydroxy Sulfones with Alkyl Aluminum Compounds: Structure of Intermediate Hydroalumination Products

open access: yesMolecules, 2022
β-Hydroxy sulfones are important in organic synthesis. The simplest method of β-hydroxy sulfones synthesis is the hydrogenation of β-keto sulfones. Herein, we report the reducing properties of alkyl aluminum compounds R3Al (R = Et, i-Bu, n-Bu, t-Bu and n-
Michał Kotecki   +6 more
doaj   +2 more sources

Two-Step Azidoalkenylation of Terminal Alkenes Using Iodomethyl Sulfones [PDF]

open access: yesMolecules, 2019
The radical azidoalkylation of alkenes that was initially developed with α-iodoesters and α-iodoketones was extended to other activated iodomethyl derivatives.
Nicolas Millius   +2 more
doaj   +2 more sources

Rongalite addition to dienones: diastereoselectivity in cyclic sulfone synthesis; stereochemical rationalization and prospects as a general conjugate nucleophile [PDF]

open access: yesBeilstein Journal of Organic Chemistry
A detailed experimental and computational study of the diastereoselectivity of cyclic sulfone synthesis by reaction of Rongalite with doubly electrophilic dienones is presented.
Melina Goga   +9 more
doaj   +2 more sources

Rh-Catalyzed Asymmetric Hydrogenation of α-Substituted Alkenyl Sulfones: Highly Chemo- and Enantioselective Access to Chiral Sulfones

open access: yesOrganic Letters, 2023
Rh–(R,R)-f-spiroPhos complex-catalyzed asymmetric hydrogenation of α-substituted alkenyl sulfones has been achieved, affording the chiral γ-keto sulfones and simple α-alkyl-substituted sulfones in high yields (96–99%) with excellent chemo ...
Xiaoxue Wu, Guofu Zi, Guohua Hou
exaly   +2 more sources

Copper-catalyzed sulfonylation of alkenes with CH3SSO3Na [PDF]

open access: yesBMC Chemistry
A successful methodology for the copper-catalyzed dehydrogenated methylsulfonylation of alkenes utilizing CH3SSO3Na in conjunction with hypervalent iodine reagents was successfully established. This method offers a practical avenue to obtain allyl methyl
Xiaoli Chen, Ge Wu
doaj   +2 more sources

Antimicrobial and Biofilm-Preventing Activity of l-Borneol Possessing 2(5H)-Furanone Derivative F131 against S. aureusC. albicans Mixed Cultures

open access: yesPathogens, 2022
Candida albicans and Staphylococcus aureus are human pathogens that are able to form mixed biofilms on the surface of mucous membranes, implants and catheters.
Rand Sulaiman   +6 more
doaj   +1 more source

Chloroaluminate Ionic Liquid Immobilized on Magnetic Nanoparticles as a Heterogeneous Lewis Acidic Catalyst for the Friedel–Crafts Sulfonylation of Aromatic Compounds

open access: yesMolecules, 2022
Chloroaluminate ionic liquid bound on magnetic nanoparticles (Fe3O4@O2Si[PrMIM]Cl·AlCl3) was prepared and used as a heterogenous Lewis acidic catalyst for the Friedel–Crafts sulfonylation of aromatic compounds with sulfonyl chlorides or p-toluenesulfonic
Ngoc-Lan Thi Nguyen   +5 more
doaj   +1 more source

A Study on the Chemistry and Biological Activity of 26-Sulfur Analogs of Diosgenin: Synthesis of 26-Thiodiosgenin S-Mono- and Dioxides, and Their Alkyl Derivatives

open access: yesMolecules, 2022
A chemoselective procedure for MCPBA oxidation of 26-thiodiosgenin to corresponding sulfoxides and sulfone was elaborated. An unusual equilibration of sulfoxides in solution was observed.
Aneta M. Tomkiel   +5 more
doaj   +1 more source

Easy Access To Allylic Sulfones Through Transition Metal-Free Hydrosulfonylation Of Allenes

open access: yes, 2021
A Brønsted acid-mediated addition of (hetero)aryl and (cyclo)alkyl sodium sulfinates to N-allenyl derivatives is described under very smooth conditions. This reaction provided a practical and efficient protocol for the synthesis of allylic sulfones in an
Marc, Taillefer   +3 more
core   +1 more source

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