Design of Modified Pyrroline N-Oxide Derivatives as Spin Traps Specific for Hydroxyl Radical

DOI: 10.1021/jo00034a020

Source and publish data:

Journal of Organic Chemistry p. 2297 - 2301 (1992)

Update date:2022-07-31

Topics:

Authors:

Arya, Prabhat

Stephens, J. Campbell

Griller, David

Pou, Sovitj

Ramos, Carroll L.

et al. et al.

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Article abstract of DOI:10.1021/jo00034a020

Nitrones, 4-<2-(ethoxycarbonyl)ethyl>-3,3,5,5-tetramethyl-1-pyrroline N-oxide (7a) and 4-<2-(ethoxycarbonyl)ethyl>-5,5-di(<2H3>methyl)-3,3-dimethyl-1-pyrroline N-oxide (7b) have been synthesized.The ability of the nitrone (7a) to spin trap hydroxyl and su

Full text of DOI:10.1021/jo00034a020

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Article Doi

Design of Modified Pyrroline N-Oxide Derivatives as Spin Traps Specific for Hydroxyl Radical

DOI: 10.1021/jo00034a020

Source and publish data:

Authors:

Article abstract of DOI:10.1021/jo00034a020

Full text of DOI:10.1021/jo00034a020

Products guided by the article

R&D Labs maybe for 139461-55-5

Relevant to this article

Synthesis and Evaluation of 2-Pyridinone Derivatives as HIV-1-Specific Reverse Transcriptase Inhibitors. 2. Analogues of 3-Aminopyridin-2(1H)-one

A simple efficient sequential one-pot intermolecular aza-Michael addition and intramolecular Buchwald-Hartwig α-arylation of amines: Synthesis of functionalized tetrahydroisoquinolines

Regioselective functionalization of the methylene group adjacent to cyclopropyl sulfide via mercury(II)-mediated regioselective ring-opening reaction

Enantioselective synthesis of 2,6-cis-disubstituted tetrahydropyrans via a tandem catalytic asymmetric hydrogenation/oxa-Michael cyclization: An efficient approach to (-)-centrolobine

Phenolic alkaloids from the aerial parts of Dracocephalum heterophyllum

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