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Volumn 17, Issue 11, 2011, Pages 3207-3212

Concise synthesis of pyrrolidine and indolizidine alkaloids by a highly convergent three-component reaction

Author keywords

alkaloids; carboazidation; iodoketones; pyrrolidines; radicals

Indexed keywords

ALKALOIDS; CARBOAZIDATION; IODOKETONES; PYRROLIDINES; RADICALS;

EID: 79952149643     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201003137     Document Type: Article
Times cited : (40)

References (51)
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    • For some examples of bioactive pyrrolidines, see
    • For some examples of bioactive pyrrolidines, see
  • 11
    • 84874434758 scopus 로고    scopus 로고
    • For reviews on pyrrolidine synthesis, see
    • For reviews on pyrrolidine synthesis, see
  • 17
    • 84874447577 scopus 로고    scopus 로고
    • For some recent indolizidine syntheses, see
    • For some recent indolizidine syntheses, see
  • 26
    • 0037119657 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2002, 41, 3460-3462.
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 3460-3462
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    • see also Si for synthesis.
    • Angew. Chem. Int. Ed. 2008, 47, 9443-9446; see also Si for synthesis.
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 9443-9446
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    • 84874425320 scopus 로고    scopus 로고
    • 2) were less efficient in the azide reduction/reductive amination cascade reaction
    • 2) were less efficient in the azide reduction/reductive amination cascade reaction.
  • 37
    • 84874446574 scopus 로고    scopus 로고
    • The corresponding product of iodine-atom transfer was obtained in 17% yield.
    • The corresponding product of iodine-atom transfer was obtained in 17 % yield.
  • 39
    • 84874411441 scopus 로고    scopus 로고
    • CCDC-786927 (4h) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • CCDC-786 927 (4 h) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via.
  • 40
    • 84874411062 scopus 로고    scopus 로고
    • For recent syntheses, see
    • For recent syntheses, see
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    • 45149147298 scopus 로고    scopus 로고
    • For a similar bis-reductive amination to Monomorine I, see
    • N. Toyooka, D. Zhou, H. Nemoto, J. Org. Chem. 2008, 73, 4575-4577. For a similar bis-reductive amination to Monomorine I, see
    • (2008) J. Org. Chem. , vol.73 , pp. 4575-4577
    • Toyooka, N.1    Zhou, D.2    Nemoto, H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.