The selective recognition-mediated reaction between a nitrone bearing a urea recognition site and a maleimide bearing a proton switchable recognition site can be turned 'on' and 'off' by the addition of base and acid respectively.

We have synthesized the fluorine-I 8 labeled derivative of N-fert-butyl-aphenylnitrone (PBN), a free radical spin trapping agent widely used with electron spin resonance (ESR). N-tert-Butyl-a-(4-[18F]fluorophenyl)nitrone ([18F]FPBN) could be prepared with low radiochemical yield (3% decay corrected) by the direct aromatic nucleophilic substitution of N-tertbutyl-a-(4-nitrophenyl)nitrone with [1...

While applying electron paramagnetic resonance (EPR)/Spin Trapping techniques, several reactive intermediate species were identified in the reaction of perfluoroisobutylene (PFIB) with nitrone and nitroso spin trap agents: the carbon dioxide radical anion (CO2.-), a carbonyl fluoride intermediate (COF), and vinyl carbanions of PFIB. The reaction of PFIB with N-t-butyl-alpha-phenylnitrone (PBN) ...

The mechanism of the addition of lithium enolates derived from esters, ketones and aldehydes to nitrones (Mannich-type reaction) has been studied using DFT methods. While the reactions with α-methoxy and α-methyl enolates takes place through a stepwise mechanism, consisting of an initial nucleophilic attack of the enolate to the nitrone carbon followed by a second nucleophilic attack of the nit...

Epimerization of C5 of an N-hydroxypyrrolidine ring by regioselective oxidation to a nitrone followed by diastereoselective reduction provides a new approach to the synthesis of swainsonine and related compounds. The only protection in the synthesis of the potent mannosidase inhibitor DIM (1,4-dideoxy-1,4-imino-d-mannitol) was the acetonation of d-mannose.

We report a draft genome sequence of Streptomyces fradiae olg1-1, a mutant strain derived from the model object S. fradiae ATCC 19609, which is resistant to nitrone-oligomycin and has a mutation in the DNA-binding domain of a transcriptional regulator PadR.

A green and sustainable nitrone formation reaction via visible-light-promoted of aryl diazoacetates with nitrosoarenes is described. This protocol exhibits good functional group tolerance broad substrate scope for both nitrosoarenes. Comparing the reported methods synthesis nitrones from nitrosoarenes, described herein occurs under sole visible-light irradiation without need any catalysts addit...

[Structure: see text] Enantioselective nitrone cycloadditions with beta-substituted alpha,beta-unsaturated 2-acyl imidazoles catalyzed by bis(oxazolinyl)pyridine-cerium(IV) triflate complexes 1 have been reported. The isoxazolidine products were efficiently transformed into densely functionalized beta'-hydroxy-beta-amino acid derivatives.

An unprecedented functionalization of multi-walled carbon nanotubes (MWCNTs) has been conveniently achieved by the 1,3-dipolar cycloaddition of a cyclic nitrone. This organic functionalization yields materials with a great solubility in DMF (close to 10 mg per mL of DMF) preferentially occurring at the defects of the MWCNT sp(2) network.

Unnatural D-amino acids bearing endocyclic nitrones were developed for live-cell labelling of the bacterial peptidoglycan layer. Metabolic incorporation of D-Lys and D-Ala derivatives bearing different endocyclic nitrones was observed in E. coli, L. innocua, and L. lactis. The incorporated nitrones of these bacteria then rapidly underwent strain-promoted alkyne-nitrone cycloaddition (SPANC) rea...