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Volumn 17, Issue 36, 2011, Pages 9907-9910

Concise construction of sarain A core according to a biosynthetic proposal: Cyclization through an intramolecular mannich-type reaction involving an endocyclic N-acyliminium ion

Author keywords

biomimetic synthesis; cyclization; diazatricycloundecane; Mannich type reaction; N acyliminium ion; sarain A

Indexed keywords

BIOMIMETIC SYNTHESIS; DIAZATRICYCLOUNDECANE; MANNICH-TYPE REACTIONS; N-ACYLIMINIUM ION; SARAIN A;

EID: 80051978385     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201101783     Document Type: Article
Times cited : (12)

References (52)
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    • 33746191902 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 2912-2915
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    • 49149121119 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 5418-5421
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 5418-5421
  • 36
    • 80051990769 scopus 로고    scopus 로고
    • For reviews on N-acyliminium ions, see
    • For reviews on N-acyliminium ions, see
  • 47
    • 0347232737 scopus 로고
    • For the intramolecular addition of a silyl enol ether onto an endocyclic N-acyliminium within a cis-fused bicyclic compound, see.
    • For the intramolecular addition of a silyl enol ether onto an endocyclic N-acyliminium within a cis-fused bicyclic compound, see:, H. Hiemstra, R. J. Vijn, W. N. Speckamp, J. Org. Chem. 1988, 53, 3882-3884.
    • (1988) J. Org. Chem. , vol.53 , pp. 3882-3884
    • Hiemstra, H.1    Vijn, R.J.2    Speckamp, W.N.3
  • 48
    • 0000803026 scopus 로고
    • Similar addition products have scarcely been isolated; see, for example
    • Similar addition products have scarcely been isolated; see, for example:, P. Cazeau, F. Duboudin, F. Moulines, O. Babot, J. Dunoguès, Tetrahedron 1987, 43, 2075-2088
    • (1987) Tetrahedron , vol.43 , pp. 2075-2088
    • Cazeau, P.1    Duboudin, F.2    Moulines, F.3    Babot, O.4    Dunoguès, J.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.