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Volumn 45, Issue 22, 2006, Pages 3683-3686

A highly enantioselective Brønsted acid catalyzed cascade reaction: Organocatalytic transfer hydrogenation of quinolines and their application in the synthesis of alkaloids

Author keywords

Asymmetric hydrogenation; Br nsted acid; Hantzsch dihydropyridine; Organocatalysis; Tetrahydroquinoline

Indexed keywords

CATALYSIS; HYDROGENATION; SUBSTITUTION REACTIONS; SYNTHESIS (CHEMICAL);

EID: 33746269442     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200600191     Document Type: Article
Times cited : (653)

References (53)
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    • (Eds.: E. N. Jacobsen, A. Pfaltz, H. Yamamoto), Springer, New York
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    • recent examples of highly enantioselective metal-catalyzed hydrogenations of imines: h) R. Kadyrov, T. H. Riermeier, Angew. Chem. 2003, 115, 5630;
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    • For reviews on chiral Brønsted acid catalysis, see: a) P. R. Schreiner, Chem. Soc. Rev. 2003, 32, 289;
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    • Schreiner, P.R.1
  • 50
    • 0000631659 scopus 로고    scopus 로고
    • For an interesting approach to 2-alkyl tetrahydroquinolines by an aza-xylene Diels-Alder reaction, see: a) H. Steinhagen, E. J. Corey, Angew. Chem. 1999, 111, 2054;
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    • Steinhagen, H.1    Corey, E.J.2
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    • note
    • The absolute 5 configuration in the case of the 2-aryl tetrahydroquinolines are based on a X-ray crystal structure of (3-bromophenyl)tetrahydroquinoline. Our corresponding optical rotation data are not in agreement with the previously reported data in Ref. [3a].


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.