Results 371 to 380 of about 538,570 (408)
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Photolysis of aryl formates and aryl acetates

Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 1979
1. The yields of the phenols during the photolysis of a number of aryl formates and aryl acetates were determined. 2. The aroxyl radicals that are obtained during the photolysis of aryl formates and aryl acetates were recorded by the pulse photolysis method. 3. The photodissociation of aryl formates and aryl acetates proceeds
G. Khageman   +4 more
openaire   +2 more sources

Deoxygenative Arylation of Carboxylic Acids by Aryl Migration

Chemistry – A European Journal, 2019
AbstractAn unprecedented deoxygenative arylation of aromatic carboxylic acids has been achieved, allowing the construction of an enhanced library of unsymmetrical diaryl ketones. The synergistic photoredox catalysis and phosphoranyl radical chemistry allows for precise cleavage of a stronger C−O bond and formation of a weaker C−C bond by 1,5‐aryl ...
Rehanguli Ruzi   +8 more
openaire   +3 more sources

Iron-Catalyzed Coupling of Aryl Sulfamates and Aryl/Vinyl Tosylates with Aryl Grignards

Organic Letters, 2014
AbstractIn contrast to previous reports with aryl chlorides, the title coupling reaction with aryl sulfamates proceeds with low levels of the Grignard homocoupling side reaction.
Toolika Agrawal, Silas P. Cook
openaire   +4 more sources

Activation of the aryl hydrocarbon receptor by structurally diverse exogenous and endogenous chemicals.

Annual Review of Pharmacology and Toxicology, 2003
The induction of expression of genes for xenobiotic metabolizing enzymes in response to chemical insult is an adaptive response found in most organisms. In vertebrates, the AhR is one of several chemical/ligand-dependent intracellular receptors that can ...
M. Denison, Scott R. Nagy
semanticscholar   +1 more source

Exploiting Aryl Mesylates and Tosylates in Catalytic Mono-α-arylation of Aryl- and Heteroarylketones

Organic Letters, 2016
AbstractKey to this general protocol for mono‐α‐arylation is the indolyl‐derived phosphine ligand which enhances the steric congestion of the catalyst.
On Ying Yuen   +4 more
openaire   +4 more sources

C-N Cross-Couplings for Site-Selective Late-Stage Diversification via Aryl Sulfonium Salts.

Journal of the American Chemical Society, 2019
We report diverse C-N cross-coupling reactions of aryl thianthrenium salts that are formed site-selectively by direct C-H functionalization. The scope of N-nucleophiles ranges from primary and secondary alkyl and aryl amines to various N-containing ...
Pascal S. Engl   +5 more
semanticscholar   +1 more source

Synthesis of Aryl Glycines by the α Arylation of Weinreb Amides

Angewandte Chemie, 2008
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 of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Olaf Panknin   +4 more
openaire   +4 more sources

Aryl–aryl coupling via directed lithiation and oxidation

Chemical Communications, 2005
AbstractFor Abstract see ChemInform Abstract in Full Text.
David R. Spring   +3 more
openaire   +4 more sources

Catalytic Scissoring of Lignin into Aryl Monomers

Advances in Materials, 2019
Lignin is an aromatic polymer, which is the biggest and most sustainable reservoir for aromatics. The selective conversion of lignin polymers into aryl monomers is a promising route to provide aromatics, but it is also a challenging task.
Min Wang, Feng Wang
semanticscholar   +1 more source

Nickel-Catalyzed Thiolation of Aryl Halides and Heteroaryl Halides through Electrochemistry.

Angewandte Chemie, 2019
Transition-metal-catalyzed coupling reactions are useful tools for synthesizing aryl sulfur compounds. However, conventional transition-metal-catalyzed thiolation of aryl bromides and chlorides typically requires the use of strong base under elevated ...
Dong Liu, Hong-Xing Ma, P. Fang, T. Mei
semanticscholar   +1 more source

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