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Volumn 42, Issue 6, 2005, Pages 1219-1222

A rhodium-catalyzed route for oxidative coupling and cyclization of 2-aminobenzyl alcohol with ketones leading to quinolines

Author keywords

[No Author keywords available]

Indexed keywords

1,2,3,4 TETRAHYDROACRIDINE; 2 (1 METHYLPROPYL)QUINOLINE; 2 AMINOBENZYL ALCOHOL; ALCOHOL; KETONE; QUINOLINE DERIVATIVE; RHODIUM COMPLEX; UNCLASSIFIED DRUG;

EID: 24944558885     PISSN: 0022152X     EISSN: None     Source Type: Journal    
DOI: 10.1002/jhet.5570420630     Document Type: Article
Times cited : (52)

References (38)
  • 23
    • 0003151465 scopus 로고
    • For a review on Friedländer quinoline synthesis: C.-C. Cheng and S.-J. Yan, Org. React., 28, 37 (1982).
    • (1982) Org. React. , vol.28 , pp. 37
    • Cheng, C.-C.1    Yan, S.-J.2
  • 26
    • 0001143726 scopus 로고
    • [11a] For transition metal-catalyzed intramolecular oxidative cyclization of 2-aminophenethyl alcohols leading to indoles: Y. Tsuji, S. Kotachi, K.-T. Huh and Y. Watanabe, J. Org. Chem., 55, 580 (1990);
    • (1990) J. Org. Chem. , vol.55 , pp. 580
    • Tsuji, Y.1    Kotachi, S.2    Huh, K.-T.3    Watanabe, Y.4
  • 29
    • 85039387141 scopus 로고    scopus 로고
    • note
    • As is the case for ruthenium-catalyzed oxidative coupling and cyclization between 1 and secondary alcohols in the presence of 1-dodecene as sacrificial hydrogen acceptor (oxidant) (ref. 10), equimolar treatment of 1 and 2a in the presence of 1-dodecene (2 mmol) as oxidant under the employed conditions afforded 3a in only 46% yield.
  • 33


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.