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Volumn , Issue 7, 2009, Pages 1099-1102

Gold(III)-catalyzed 1,4-nucleophilic addition: Facile approach to prepare 2-amino-1,4-naphthalenedione and 6-amino-5,8-quinolinedione derivatives

Author keywords

2 amino 1,4 naphthalenedione; 6 amino 5,8 quinolinedione; Sodium tetrachloroaurate

Indexed keywords

2 AMINO 1,4 NAPHTHALENEDIONE; 2 BUTYNYLAMINE; 6 AMINO 5,8 QUINOLINEDIONE DERIVATIVE; ALLYLAMINE; AROMATIC AMINE; GOLD DERIVATIVE; NAPHTHALENE; NUCLEOPHILE; QUINOLINE; UNCLASSIFIED DRUG;

EID: 67649411655     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0028-1088116     Document Type: Article
Times cited : (22)

References (31)
  • 16
  • 29
    • 0026677093 scopus 로고
    • When the reaction performed in DMF without any catalyst, the yield reported is 72% after 24 h. For the reference, see
    • When the reaction performed in DMF without any catalyst, the yield reported is 72% after 24 h. For the reference, see: Aristoff, P. A.; Johnson, P. D. J. Org. Chem. 1992, 57, 6234.
    • (1992) J. Org. Chem. , vol.57 , pp. 6234
    • Aristoff, P.A.1    Johnson, P.D.2
  • 30
    • 67649414716 scopus 로고    scopus 로고
    • note
    • 4, and the solvent was removed by distillation. The crude products obtained were purified by flash chromatography to give 2-amino-1,4-naphthalenediones and 6-amino-5,8-quinolinediones.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.