a-amino-uv stabilizedd radical 为什么阿尔法胺基可以稳定自由基

【图文】物理有机化学--自由基_百度文库
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a-amino-stabilized radical
为什么阿尔法胺基可以稳定自由基
如题,也就是说下图的加成产物为什么是7而不是烷基加在阿尔法碳上?
哈哈是缩合吧
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, 8 October 2014, Pages
Synthesis of 2-pyrolyl-2-hydroxy-2-cyanoacetamide through FeCl3&TBHP mediated hydroxylation of captodative stabilized radical intermediate, ,
Department of Chemistry, University of Calcutta, 92, A. P. C. Road, Kolkata 700 009, IndiaA series of 2-hydroxy-2-(4-oxo-1,2-diaryl-4,5,6,7-tetrahydro-1H-3-indolyl)-2-cyanoacetamides have been synthesized through selective CH oxidation of active methylene carbon of cyanoacetamide derivatives using tert-butyl hydroperoxide as oxidant and ferric chloride as radical initiator. In this reaction the tert-butyl oxo radical abstracts hydrogen from the active methylene group of 2-pyrolyl-2-cyanoacetamides to generate a stable captodative radical intermediate. Then recombination of this radical intermediate with tert-butyl oxo radical followed by acid catalysed thermal elimination of the tert-butyl group produces the quaternary hydroxyl cyanoacetamide derivatives in good yield.KeywordsHydroxylation; TBHP&FeCl3; Radical pathway; 2-Hydroxy-2-cyanoacetamide; Captodative radicals
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