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Volumn 47, Issue 38, 2006, Pages 6781-6785

A copper(II)-catalyzed protocol for modified Friedländer quinoline synthesis

Author keywords

2 Aminobenzyl alcohol; Aldehydes; Copper catalyst; Ketones; Quinolines

Indexed keywords

2 AMINOBENZYL ALCOHOL; ALCOHOL DERIVATIVE; ALDEHYDE DERIVATIVE; ARGON; CUPRIC ION; DIOXANE; KETONE DERIVATIVE; OXYGEN; QUINOLINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 33747158781     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.07.067     Document Type: Article
Times cited : (78)

References (36)
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    • For our recent report on synthesis of indoles via similar ruthenium-catalyzed alkanol group transfer from alkanolamines to N-atom of anilines:
    • For our recent report on synthesis of indoles via similar ruthenium-catalyzed alkanol group transfer from alkanolamines to N-atom of anilines:. Cho C.S., Lim H.K., Shim S.C., Kim T.J., and Choi H.-J. Chem. Commun. (1998) 995
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    • For similar ruthenium- and iridium-catalyzed oxidative cyclization of 2-aminobenzyl alcohol with ketones leading to quinolines:
    • For similar ruthenium- and iridium-catalyzed oxidative cyclization of 2-aminobenzyl alcohol with ketones leading to quinolines:. Motokura K., Mizugaki T., Ebitani K., and Kaneda K. Tetrahedron Lett. 45 (2004) 6029
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    • Motokura, K.1    Mizugaki, T.2    Ebitani, K.3    Kaneda, K.4
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    • It has recently been found that carbonyl compounds (or secondary alcohols) are coupled with primary alcohols in the presence of a ruthenium catalyst and a base:
    • It has recently been found that carbonyl compounds (or secondary alcohols) are coupled with primary alcohols in the presence of a ruthenium catalyst and a base:. Cho C.S., Kim B.T., Kim T.-J., and Shim S.C. J. Org. Chem. 66 (2001) 9020
    • (2001) J. Org. Chem. , vol.66 , pp. 9020
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    • For ruthenium-catalyzed oxidative cyclization of 2-aminobenzyl alcohol with aldehydes leading to 3-substituted quinolines
    • For ruthenium-catalyzed oxidative cyclization of 2-aminobenzyl alcohol with aldehydes leading to 3-substituted quinolines. Cho C.S., Ren W.X., and Shim S.C. Bull. Korean Chem. Soc. 26 (2005) 2038
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  • 35
  • 36
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    • note
    • 2/KOH catalytic system, however, benzyl alcohol was not effectively oxidized to benzaldehyde (11% yield) under the same catalytic system.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.