Synthesis of the radical scavenger 1,1,3,3-Tetramethylisoindolin-2-yloxyl
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A versatile free-radical trapping agent, 1,1,3,3-tetramethylisoindolin-2-yloxyl, has been prepared from N-benzylphthalimide by reaction with 'methylmagnesium iodide' in refluxing toluene followed by hydrogenolysis and oxidation. The Grignard reaction gives 2-benzyl-1,1,3,3-tetramethylisoindoline along with a small proportion of an unexpected by-product, 2-benzyl-1-ethyl-1,3,3-trimethyliso-indoline.
2002 ◽
Vol 11
(1)
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pp. 34-42
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2002 ◽
Vol 58
(6)
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pp. 409-415
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1991 ◽
Vol 15
(3)
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pp. 177-186
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2004 ◽
Vol 312
(2)
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pp. 774-779
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2005 ◽
Vol 25
(1_suppl)
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pp. S30-S30
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