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Volumn 50, Issue 39, 2011, Pages 9177-9179

A synthetic study of atropurpuran: Construction of a pentacyclic framework by an intramolecular reverse-electron-demand diels-alder reaction

Author keywords

benzoquinones; Diels Alder reaction; pentacycles; synthetic methods; terpenoids

Indexed keywords

BENZOQUINONES; DIELS-ALDER REACTION; PENTACYCLES; SYNTHETIC METHODS; TERPENOIDS;

EID: 80052848426     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201103950     Document Type: Article
Times cited : (33)

References (16)
  • 11
    • 79955397100 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2011, 50, 4068-4093.
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 4068-4093
  • 12
    • 77954119213 scopus 로고    scopus 로고
    • For an example of our study, see.
    • For an example of our study, see:, T. Suzuki, S. Kobayashi, Org. Lett. 2010, 12, 2920-2923.
    • (2010) Org. Lett. , vol.12 , pp. 2920-2923
    • Suzuki, T.1    Kobayashi, S.2
  • 15
    • 84856545935 scopus 로고    scopus 로고
    • A torsion angle of 146.3° for the C10-C9-C11-C12 bonds is consistent with our previous observation on an E-olefin that contains an eight-membered ring, see
    • A torsion angle of 146.3° for the C10-C9-C11-C12 bonds is consistent with our previous observation on an E-olefin that contains an eight-membered ring, see:, R. Matsui, K. Seto, K. Fujita, T. Suzuki, A. Nakazaki, S. Kobayashi, Angew. Chem. 2010, 122, 10266-10271
    • (2010) Angew. Chem. , vol.122 , pp. 10266-10271
    • Matsui, R.1    Seto, K.2    Fujita, K.3    Suzuki, T.4    Nakazaki, A.5    Kobayashi, S.6
  • 16
    • 78650467062 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2010, 49, 10068-10073.
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 10068-10073


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.