Results 21 to 30 of about 408,472 (346)

2-aminophenols containing electron-withdrawing groups from N-aryl hydroxylamines [PDF]

open access: yes, 2010
Reaction of substituted N-aryl hydroxylamines with methanesulfonyl chloride, p-toluenesulfonyl chloride, or trifluoromethanesulfonic anhydride under basic conditions leads to the rearranged 2-aminophenols (45-94%).
Cooper, Anthony W. J.   +3 more
core   +1 more source

Synthesis of 2-aryl-benzothiazoles via Ni-catalyzed coupling of benzothiazoles and aryl sulfamates

open access: yesHeterocyclic Communications, 2020
2-Aryl-benzothiazoles have been successfully synthesized via a simple coupling reaction between benzothiazoles and aryl sulfamates using a nickel catalyst. The nickel catalyst is inexpensive, reusable and commercially available.
Yu Xiaofeng   +4 more
doaj   +1 more source

One-pot radioiodination of aryl amines via stable diazonium salts: preparation of 125I-imaging agents [PDF]

open access: yes, 2017
An operationally simple, one-pot, two-step tandem procedure that allows the incorporation of radioactive iodine into aryl amines via stable diazonium salts is described.
Luthra, Sajinder K.   +4 more
core   +2 more sources

Direct acylation of aryl amines using dimethylformamide and dimethylacetamide as the acyl resources

open access: yesJournal of Saudi Chemical Society, 2016
The treatment of aryl amines with dimethylformamide (DMF) and dimethylacetamide (DMA) in the presence of hydrochloric acid brings about efficient N-acylation to give the corresponding aryl formamides and aryl acetamides in acceptable to excellent yields.
Qing Zhang, Cui Chen
doaj   +1 more source

Palladium-catalyzed acetylation of arenes. [PDF]

open access: yes, 2014
A simple method for the preparation of aryl methyl ketones is reported. The transformation involves the Pd-catalyzed coupling of an acyl anion equivalent, acetyltrimethylsilane, with aryl bromides to afford the corresponding acetylated arenes in ...
Garg, Neil K, Ramgren, Stephen D
core   +1 more source

Microwave-mediated synthesis of N-methyliminodiacetic acid (MIDA) boronates [PDF]

open access: yes, 2014
A library of over 20, mainly aryl or heteroaryl, N-methyliminodiacetic acid (MIDA) boronates have been synthesised. A rapid microwave-mediated (MW) method (5–10 min) has been developed using polyethylene glycol 300 (PEG 300) as solvent.
Close, Adam J   +3 more
core   +1 more source

Nucleophilic Substitution on 2-Monosubstituted Quinoxalines Giving 2,3-Disubstituted Quinoxalines: Investigating the Effect of the 2-Substituent

open access: yesMolecules, 2016
An investigation on the effect of substituent at the 2-position of mono-substituted quinoxalines in the synthesis of di-substituted quinoxaline derivatives via nucleophilic substitution reactions, is reported.
Ndumiso Thamsanqa Ndlovu   +1 more
doaj   +1 more source

Intra- and Intermolecular C−H Activation by Bis(phenolate)pyridineiridium(III) Complexes [PDF]

open access: yes, 2011
A bis(phenolate)pyridine pincer ligand (henceforth abbreviated as ONO) has been employed to support a variety of iridium complexes in oxidation states I, III, and IV.
Bercaw, John E.   +2 more
core   +2 more sources

Palladium-Catalyzed α-Arylation of Aryl Nitromethanes

open access: yesOrganic Letters, 2015
Catalytic conditions for the α-arylation of aryl nitromethanes have been discovered using parallel microscale experimentation, despite two prior reports of the lack of reactivity of these aryl nitromethane precursors. The method efficiently provides a variety of substituted, isolable diaryl nitromethanes.
VanGelder, Kelsey F.   +1 more
openaire   +2 more sources

An isoxazole strategy for the synthesis of 4-oxo-1,4-dihydropyridine-3-carboxylates

open access: yesBeilstein Journal of Organic Chemistry, 2022
A method has been developed for the preparation of 2-alkyl-6-aryl-, 2-aryl-6-aryl and 2,6-diaryl-5-aryl/hetaryl-substituted methyl 4-oxo-1,4-dihydropyridine-3-carboxylates by Mo(CO)6-mediated ring expansion of methyl 2-(isoxazol-5-yl)-3-oxopropanoates ...
Timur O. Zanakhov   +3 more
doaj   +1 more source

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