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Volumn 40, Issue 36, 1999, Pages 6513-6516

Studies towards the total synthesis of halichlorine: Asymmetric synthesis of the spiroquinolizidine subunit

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOID; CHLORINE DERIVATIVE; LACTAM DERIVATIVE; MANNICH BASE; NATURAL PRODUCT; QUINOLIZIDINE DERIVATIVE; SPIRO COMPOUND;

EID: 0033520211     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)01170-3     Document Type: Article
Times cited : (60)

References (25)
  • 5
  • 11
    • 0003417469 scopus 로고
    • Trost, B. M.; Fleming, I., Eds.; Pergamon: Oxford, Chapter 4.5
    • For a review of additions to N-acyliminium ions, see: Hiemstra, H.; Speckamp, W. N. In Comprehensive Organic Synthesis; Trost, B. M.; Fleming, I., Eds.; Pergamon: Oxford, 1991; Vol. 2, Chapter 4.5.
    • (1991) Comprehensive Organic Synthesis , vol.2
    • Hiemstra, H.1    Speckamp, W.N.2
  • 13
    • 2042507954 scopus 로고
    • For a comprehensive review of the Suzuki reaction, see: (a) Miyaura, N.; Suzuki, A. Chem. Rev. 1995, 95, 2457.
    • (1995) Chem. Rev. , vol.95 , pp. 2457
    • Miyaura, N.1    Suzuki, A.2
  • 18
    • 0009642172 scopus 로고    scopus 로고
    • Similarly, reaction of 12 with the corresponding E-iodoacrylate under otherwise identical conditions furnished the E-alkenoate which again underwent highly diastereoselective ring closure to afford a 16:1 mixture of 14 and its C5-epimer.
    • Similarly, reaction of 12 with the corresponding E-iodoacrylate under otherwise identical conditions furnished the E- alkenoate which again underwent highly diastereoselective ring closure to afford a 16:1 mixture of 14 and its C5-epimer.
  • 22
    • 0009620906 scopus 로고    scopus 로고
    • note
    • 3): δ=20.32, 22.59, 25.23, 29.22, 30.78, 33.85, 35.24, 35.95, 40.34, 42.24, 47.53, 53.39, 62.91, 69.43, 69.82, 81.43, 130.22, 136.21, 165.88.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.