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Iron and Ruthenium Lewis Acid Catalyzed Asymmetric 1,3-Dipolar Cycloaddition Reactions between Nitrones and Enals

The single coordination-site transition metal Lewis acids [CpM(BIPHOP-F)][SbF6] (M = Fe, Ru) catalyze the [3+2] dipolar cycloaddition reaction between reactive nitrones and α,β-unsaturated aldehydes to give chiral isoxazolidines with ee values of 75 to >96%. The stereochemistry of the major enant...

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Published in:Journal of the American Chemical Society 2002-05, Vol.124 (18), p.4968-4969
Main Authors: Viton, Florian, Bernardinelli, Gérald, Kündig, E. Peter
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cited_by cdi_FETCH-LOGICAL-a445t-bd1e40dbe348c285313ec7694cfa0ac855e8bea1189c57f2d11dbebb8375638f3
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container_end_page 4969
container_issue 18
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container_title Journal of the American Chemical Society
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creator Viton, Florian
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Kündig, E. Peter
description The single coordination-site transition metal Lewis acids [CpM(BIPHOP-F)][SbF6] (M = Fe, Ru) catalyze the [3+2] dipolar cycloaddition reaction between reactive nitrones and α,β-unsaturated aldehydes to give chiral isoxazolidines with ee values of 75 to >96%. The stereochemistry of the major enantiomer is consistent with an endo approach of the nitrone to the Cα-Si-face of the enal in the s-trans conformation in the (R,R)-catalyst site. The absolute configuration is based on an X-ray structure determination.
doi_str_mv 10.1021/ja017814f
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source American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)
subjects Acrolein - analogs & derivatives
Acrolein - chemistry
Catalysis
Chemistry
Exact sciences and technology
Iron - chemistry
Isoxazoles - chemical synthesis
Models, Molecular
Nitrogen Oxides - chemistry
Organic chemistry
Organometallic Compounds - chemistry
Ruthenium - chemistry
Stereoisomerism
title Iron and Ruthenium Lewis Acid Catalyzed Asymmetric 1,3-Dipolar Cycloaddition Reactions between Nitrones and Enals
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