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Volumn 357, Issue 11, 2015, Pages 2529-2539

Tert-Butyl Hydroperoxide and Tetrabutylammonium Iodide-Promoted Free Radical Cyclization of α-Imino-N-arylamides and α-Azido-N-arylamides

Author keywords

(N arylcarbamyl) 2 iminoacetates; iminyl radicals; oxidative cyclization; tert butyl hydroperoxide; tetrabutylammonium iodide; azido N arylacetamide

Indexed keywords


EID: 84938983447     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201500305     Document Type: Article
Times cited : (28)

References (75)
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    • Li, D.1    Yang, T.2    Su, H.3    Yu, W.4
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    • Adv. Synth. Catal. 2015, 357, 601. The main reason why we wrongly assigned the structures of 1 was that, in MS measurement of the first batch of compounds, compound 1p showed a molecular weight of 370.1863 (calcd. for C19H20N4O3+NH4: 370.1874), indicating the existence of N3 group. Later on, this measurement was proved to be wrong. We let the sample of the same molecule be measured two more times, and both datasets showed the loss of N2. The convincing evidence for the structural difference between 1 and 7 came from the FT-IR data (see the Supporting Information). In the FT-IR spectra of 7, a strong sharp peak appears at about 2100 cm-1, which is caused by the absorption of the N3 group, whereas in the FT-IR spectra of 1, this peak is absent. In the latter cases, an absorption corresponding to an N-H stretch vibration appears at about 3200 cm-1. We apologize for these terrible mistakes in the previous paper caused by our negligence.
    • (2015) Adv. Synth. Catal. , vol.357 , pp. 601
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.