메뉴 건너뛰기




Volumn 10, Issue 11, 2004, Pages 2722-2731

Enantioselective total syntheses of the Ipecacuanha alkaloid emetine, the Alangium alkaloid tubulosine and a novel benzoqainolizidine alkaloid by using a domino process

Author keywords

Alkaloids; Asymmetric catalysis; Domino reactions; Hydrogenation; Imines; Natural products

Indexed keywords

ADDITION REACTIONS; CATALYSIS; CATALYSTS; HYDROGENATION; SYNTHESIS (CHEMICAL);

EID: 3042577737     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/chem.200306039     Document Type: Article
Times cited : (120)

References (47)
  • 19
    • 0001237986 scopus 로고
    • a) L. F. Tietze, U. Beifuß, Angew. Chem. 1993, 105, 137-170; Angew. Chem. Int. Ed. Engl. 1993, 32, 131-163;
    • (1993) Angew. Chem. , vol.105 , pp. 137-170
    • Tietze, L.F.1    Beifuß, U.2
  • 20
    • 33750173220 scopus 로고
    • a) L. F. Tietze, U. Beifuß, Angew. Chem. 1993, 105, 137-170; Angew. Chem. Int. Ed. Engl. 1993, 32, 131-163;
    • (1993) Angew. Chem. Int. Ed. Engl. , vol.32 , pp. 131-163
  • 24
    • 2442453931 scopus 로고    scopus 로고
    • (Eds.: F. Vögtle, J. F. Stoddart, M. Shibasaki), Wiley-VCH, Weinheim
    • L. F. Tietze, F. Haunert in Stimulating Concepts in Chemistry (Eds.: F. Vögtle, J. F. Stoddart, M. Shibasaki), Wiley-VCH, Weinheim, 2000, pp. 40-64.
    • (2000) Stimulating Concepts in Chemistry , pp. 40-64
    • Tietze, L.F.1    Haunert, F.2
  • 27
    • 0000415230 scopus 로고    scopus 로고
    • c) L. F. Tietze, Y. Zhou, Angew. Chem. 1999, 111, 2076-2078; Angew. Chem. Int. Ed. 1999, 38, 2045-2047;
    • (1999) Angew. Chem. , vol.111 , pp. 2076-2078
    • Tietze, L.F.1    Zhou, Y.2
  • 28
    • 0033549505 scopus 로고    scopus 로고
    • c) L. F. Tietze, Y. Zhou, Angew. Chem. 1999, 111, 2076-2078; Angew. Chem. Int. Ed. 1999, 38, 2045-2047;
    • (1999) Angew. Chem. Int. Ed. , vol.38 , pp. 2045-2047
  • 30
    • 0035793678 scopus 로고    scopus 로고
    • d) L. F. Tietze, H. Evers, E. Töpken, Angew. Chem. 2001, 113, 903-905; Angew. Chem. Int. Ed. 2001, 40, 927-929.
    • (2001) Angew. Chem. Int. Ed. , vol.40 , pp. 927-929
  • 32
    • 0141857216 scopus 로고    scopus 로고
    • L. F. Tietze, N. Rackelmann, G. Sekar, Angew. Chem. 2003, 115, 4386-4389; Angew. Chem. Int. Ed. 2003, 42, 4254-4257;
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 4254-4257
  • 35
    • 3042670346 scopus 로고    scopus 로고
    • note
    • -3, absolute structure parameter=-0.2(13). CCDC-226496 (4) and CCDC-226497 (22) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge via www.ccdc.cam.ac.uk/conts/retrieving.html (or from the Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB21EZ, UK; fax: (+44)1223-336-033; or deposit@ccdc.cam.uk).
  • 44
    • 3042572593 scopus 로고    scopus 로고
    • note
    • Sample of tubulosine, provided by Prof. T. Tanahashi, Kobe Pharmaceutical University, Japan.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.