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Volumn 37, Issue 1-2, 1998, Pages 104-105

Expeditious Enantioselective Biomimetic Synthesis of the Nitrarta Alkaloids (+)-Isonitramine and (-)-Sibirine

Author keywords

Alkaloids; Asymmetric synthesis; Biomimetic synthesis; Natural products; Spiro compounds

Indexed keywords


EID: 0031929582     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1521-3773(19980202)37:1/2<104::AID-ANIE104>3.0.CO;2-K     Document Type: Article
Times cited : (49)

References (19)
  • 5
    • 0029011164 scopus 로고
    • and references therein
    • c) M. Keppens, N. De Kimpe, J. Org. Chem. 1995, 60, 3916-3918, and references therein;
    • (1995) J. Org. Chem. , vol.60 , pp. 3916-3918
    • Keppens, M.1    De Kimpe, N.2
  • 12
    • 0346134834 scopus 로고    scopus 로고
    • Crystallographic data (excluding structure factors) for the structure reported in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication no. CCDC-100 690. Copies of the data can be obtained free of charge on application to CCDC, 12 Union Road, Cambridge CB21EZ, UK (fax: int. code + (1223)336-033; e-mail: deposit@ccdc.cam.ac.uk)
    • Crystallographic data (excluding structure factors) for the structure reported in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication no. CCDC-100 690. Copies of the data can be obtained free of charge on application to CCDC, 12 Union Road, Cambridge CB21EZ, UK (fax: int. code + (1223)336-033; e-mail: deposit@ccdc.cam.ac.uk).
  • 18
    • 0346765359 scopus 로고    scopus 로고
    • note
    • Isonitramine (-)-1 could be obtained in a single step by treating 3 with Raney nickel at 80°C and 25 bar in THF; however, the yield was modest (20%, not optimized).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.