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Volumn 2, Issue 8, 2000, Pages 1023-1026

Intramolecular Diels-Alder cyclizations of (E)-1-nitro-1,7,9-decatrienes: Synthesis of the AB ring system of norzoanthamine

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOID; AZEPINE DERIVATIVE; FUSED HETEROCYCLIC RINGS; NORZOANTHAMINE; QUINOLINE DERIVATIVE;

EID: 0034689855     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol9904085     Document Type: Article
Times cited : (53)

References (34)
  • 1
    • 0000048482 scopus 로고
    • Trost, B. M., Fleming, I., Eds.; Pergamon Press: New York
    • For reviews of the intramolecular Diels-Alder reaction, see: (a) Roush, W. R. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds., Pergamon Press: New York, 1991; Vol. 5, pp 513-550.
    • (1991) Comprehensive Organic Synthesis , vol.5 , pp. 513-550
    • Roush, W.R.1
  • 13
    • 0001053365 scopus 로고    scopus 로고
    • (b) For a review of tandem [4 + 2]/[3 + 2] cycloaddition reactions of nitroalkenes, see: Denmark, S. E.; Thorarensen, A. Chem. Rev. 1996, 96, 137.
    • (1996) Chem. Rev. , vol.96 , pp. 137
    • Denmark, S.E.1    Thorarensen, A.2
  • 26
    • 85088716456 scopus 로고    scopus 로고
    • 13C NMR, IR, HRMS, and optical rotation where appropriate. Yields are for isolated, chromatographically pure products
    • 13C NMR, IR, HRMS, and optical rotation where appropriate. Yields are for isolated, chromatographically pure products.
  • 33
    • 0041750993 scopus 로고    scopus 로고
    • Molecular mechanics calculations were performed using the MacroModel program version 7.0 (MM2* force-field)
    • Molecular mechanics calculations were performed using the MacroModel program version 7.0 (MM2* force-field).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.