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Volumn , Issue 3, 2000, Pages 374-378

Sequential Suzuki/Suzuki couplings with a dibromoiododiene - A versatile strategy for the stereocontrolled synthesis of polyunsaturated butenolides

Author keywords

Butenolides; C C couplings; Furanones; Stereoselective synthesis; Suzuki couplings

Indexed keywords

ALKADIENE; BUTENOLIDE;

EID: 0038246569     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (34)

References (42)
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    • f) C. Harcken, T. Berkenbusch, S. Braukmüller, A. Umland, K. Siegel, F. Görth, F. von der Ohe, R. Brückner, in "Current Trends in Organic Synthesis" (C. Scolastico, F. Nicotra, Edts.), Plenum Press 1999, 153-161.-Another application of this strategy is due to H. Takayama, T. Kuwajima, M. Kitajima, M. G. Nonato, N. Aimi, Heterocycles 1999, 50, 75-78.-Key references to conceptually different syntheses of γ-alkylidenebutenolides: E.-i. Negishi, M. Kotora, Tetrahedron 1997, 53, 6707-6738; R. Rossi, F. Bellina, M. Biagetti, L. Mannina, Tetrahedron Lett. 1998, 39, 7799-7802; C Xu, E.-i. Negishi, Tetrahedron Lett. 1999, 40, 431-434.
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    • f) C. Harcken, T. Berkenbusch, S. Braukmüller, A. Umland, K. Siegel, F. Görth, F. von der Ohe, R. Brückner, in "Current Trends in Organic Synthesis" (C. Scolastico, F. Nicotra, Edts.), Plenum Press 1999, 153-161.-Another application of this strategy is due to H. Takayama, T. Kuwajima, M. Kitajima, M. G. Nonato, N. Aimi, Heterocycles 1999, 50, 75-78.-Key references to conceptually different syntheses of γ-alkylidenebutenolides: E.-i. Negishi, M. Kotora, Tetrahedron 1997, 53, 6707-6738; R. Rossi, F. Bellina, M. Biagetti, L. Mannina, Tetrahedron Lett. 1998, 39, 7799-7802; C Xu, E.-i. Negishi, Tetrahedron Lett. 1999, 40, 431-434.
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    • 0033555262 scopus 로고    scopus 로고
    • f) C. Harcken, T. Berkenbusch, S. Braukmüller, A. Umland, K. Siegel, F. Görth, F. von der Ohe, R. Brückner, in "Current Trends in Organic Synthesis" (C. Scolastico, F. Nicotra, Edts.), Plenum Press 1999, 153-161.-Another application of this strategy is due to H. Takayama, T. Kuwajima, M. Kitajima, M. G. Nonato, N. Aimi, Heterocycles 1999, 50, 75-78.-Key references to conceptually different syntheses of γ-alkylidenebutenolides: E.-i. Negishi, M. Kotora, Tetrahedron 1997, 53, 6707-6738; R. Rossi, F. Bellina, M. Biagetti, L. Mannina, Tetrahedron Lett. 1998, 39, 7799-7802; C Xu, E.-i. Negishi, Tetrahedron Lett. 1999, 40, 431-434.
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  • 29
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    • note
    • 2], 79.02, 81.42 and 83.11 (C-1, C-4′, C-5′), 94.83 (C-2′), 110.08 (C-2′), 134.81 (C-1″), 142.56 (C-2).
  • 32
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    • (Eds.: F. Diederich, P. Stang), Wiley-VCH, Weinheim
    • c) A. Suzuki, in Metal-Catalyzed Cross-Coupling Reactions (Eds.: F. Diederich, P. Stang), Wiley-VCH, Weinheim 1998, 49-97.
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    • Suzuki, A.1
  • 35
    • 0343694282 scopus 로고    scopus 로고
    • note
    • meta), 129.10 (C-3), 132.18 and 137.29 (C-4, ipso-C), 133.62 (C-1), 135.27 (C-1″).
  • 38
    • 0342389030 scopus 로고    scopus 로고
    • note
    • meta), 128.65 (C-3), 129.58, 133.01 and 137.41 (C-4, C-2″, ipso-C), 133.09 (C-1), 143.81 (C-4″).
  • 39
    • 0343694277 scopus 로고    scopus 로고
    • note
    • aromatic), 133.19, 137.50 and 137.61 (C-2, C-1″″, ipso-C), 167.14 (C-1).
  • 40
    • 0342389029 scopus 로고    scopus 로고
    • note
    • aromatic), 128.93 (C-3‴), 130.96, 134.60 and 137.11 (C-3, C-2‴, ipso-C), 134.07 (C-5‴), 142.35 (C-4), 144.51 (C-2), 171.56 (C-2).
  • 41
    • 0342823829 scopus 로고    scopus 로고
    • note
    • aromatic), 126.78, 134.18 and 137.20 (C-3, C-2‴, ipso-C), 134.44 (C-4), 135.63 (C-5‴), 137.02 (C-3‴), 144.88 (C-2′), 147.10 (C-5), 169.14 (C-2).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.