Results 1 to 10 of about 3,323 (237)

Comparative Nitrene-Transfer Chemistry to Olefins Mediated by First-Row Transition Metal Catalysts Supported by a Pyridinophane Macrocycle with N4 Ligation [PDF]

open access: yesMolecules
A 12-membered pyridinophane scaffold containing two pyridine and two tertiary amine residues is examined as a prototype ligand (tBuN4) for supporting nitrene transfer to olefins.
Himanshu Bhatia   +6 more
doaj   +2 more sources

Ligand-controlled regiodivergent and enantioselective hydrophosphorylation of styrenes by palladium [PDF]

open access: yesNature Communications
Asymmetric hydrophosphorylation of unsaturated compounds is a straightforward and atom-economic approach to obtain chiral organophosphorus compounds.
Chun Ma   +4 more
doaj   +2 more sources

Silver‐Catalyzed Decarboxylative Coupling of Oxamic Acids with Styrenes to Synthesize E‐Cinnamamides: A Distinguish Reaction Pathway [PDF]

open access: yesChemistryOpen
A silver‐catalyzed decarboxylative coupling of oxamic acids with styrenes has been developed to produce E‐cinnamamides. Oxamic acids act as efficient precursors for carbamoy radicals.
Ru‐Han A   +2 more
doaj   +2 more sources

A three-step, one-pot strategy to unsymmetrical 1,1-diarylalkenes [PDF]

open access: yesBMC Research Notes
Objective Develop a one-pot, three-step procedure for effective access to diverse unsymmetrical 1,1-diarylalkenes from readily accessible reagents, catalysts and substrates.
Vijayaragavan Elumalai   +5 more
doaj   +2 more sources

Atropisomerism in Styrene: Synthesis, Stability, and Applications

open access: yesSynOpen, 2021
Atropisomeric styrenes are a class of optically active compounds, the chirality of which results from restricted rotation of the C(vinyl)–C(aryl) single bond.
Jia Feng, Zhenhua Gu
doaj   +1 more source

Frustrated Lewis pair catalyzed C–F activation of α-trifluoromethylstyrenes

open access: yesTetrahedron Chem, 2023
A frustrated Lewis pair approach is used for the monoselective C–F activation of α-trifluoromethyl styrenes. Selective C–F activation of α-trifluoromethyl styrenes with trispentafluorophenylborane (BCF) in partnership with tri(ortho-tolyl)phosphine or 2 ...
Chakyu Richard Chan   +2 more
doaj   +1 more source

Olefin–Styrene Copolymers [PDF]

open access: yesPolymers, 2016
In this review are reported some of the most relevant achievements in the chemistry of the ethylene–styrene copolymerization and in the characterization of the copolymer materials. Focus is put on the relationship between the structure of the catalyst and that of the obtained copolymer.
GALDI, NUNZIA   +2 more
openaire   +2 more sources

Controllable Synthesis of Trifluoromethyl- or gem-Difluorovinyl-containing Analogues of Neonicotinoids by the Reaction of α-(Trifluoromethyl)styrenes with 2-Nitroimino-imidazolidine

open access: yesMolecules, 2023
A simple and straightforward addition or defluorination of α-(trifluoromethyl)styrenes with 2-nitroimino-imidazolidine (2a), 2-(nitromethylene)imidazolidine (2b), 2-cyanoimino-thiazolidine (2c), and (E)-1-methyl-2-nitroguanidine (2d), in a controlled ...
Jingjing He   +5 more
doaj   +1 more source

Enantioselective organocatalytic synthesis of axially chiral aldehyde-containing styrenes via SNAr reaction-guided dynamic kinetic resolution

open access: yesNature Communications, 2023
The precise and efficient construction of axially chiral scaffolds, particularly toward the aryl-alkene atropoisomers with impeccably full enantiocontrol and highly structural diversity, remains greatly challenging. Herein, we disclose an organocatalytic
Fengyuan Guo   +4 more
doaj   +1 more source

Carbene-catalyzed atroposelective synthesis of axially chiral styrenes

open access: yesNature Communications, 2022
Axially chiral styrenes bearing a chiral axis between a sterically non-congested acyclic alkene and an aryl ring are difficult to prepare due to low rotational barrier of the axis. Here the authors present a method to form axially chiral styrenes bearing
Jia-Lei Yan   +8 more
doaj   +1 more source

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