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Volumn 18, Issue 18, 2012, Pages 5530-5535

Gold(I)-catalyzed unprecedented rearrangement reaction between 2-aminobenzaldehydes with propargyl amines: An expedient route to 3-aminoquinolines

Author keywords

3 aminoquinolines; alkynes; density functional calculations; gold; rearrangement

Indexed keywords

3-AMINOQUINOLINES; ALKYNES; DESIGNED EXPERIMENTS; DFT CALCULATION; ONE STEP; PROPARGYL; REARRANGEMENT; REARRANGEMENT REACTIONS;

EID: 84859894424     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201103668     Document Type: Article
Times cited : (28)

References (78)
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    • It also possible that 2-aminomethylquinoline (Scheme 1, b) forms first, which then rearranges to 3-amino-2-methylquinoline (Scheme 1, c) in the presence of Au salts. To ascertain this possibility, 2-aminomethylquinoline was treated under Au-catalyzed standard conditions. However, the formation of product was not observed and the starting material was recovered in quantitative yield. This led us to conclude that the 2-aminomethylquinoline is not the intermediate of the present reaction. The 2-Aminomethylquinoline used in this study was prepared using a procedure reported by Comba and co-workers, see:, P. Comba, C. Lang, C. L. de Laorden, A. Muruganantham, G. Rajaraman, H. Wadepohl, M. Zajaczkowski, Chem. Eur. J. 2008, 14, 5313-5328.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.