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Volumn 71, Issue 22, 2006, Pages 8658-8660

Gold-catalyzed and N-iodosuccinimide-mediated cyclization of γ-substituted allenamides

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSIS; GAMMA RAYS; GOLD; REACTION KINETICS; STEREOCHEMISTRY;

EID: 33750454122     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo061340r     Document Type: Article
Times cited : (89)

References (16)
  • 4
    • 0036126987 scopus 로고    scopus 로고
    • For a review on nucleophilic transition-metal-based cyclization of allenes, see: Bates, R. W.; Satcharoen, V. Chem. Soc. Rev. 2002, 31, 12.
    • (2002) Chem. Soc. Rev. , vol.31 , pp. 12
    • Bates, R.W.1    Satcharoen, V.2
  • 6
    • 33750489242 scopus 로고    scopus 로고
    • note
    • 4.
  • 7
    • 33750441326 scopus 로고    scopus 로고
    • note
    • The structure of this compound was determined by X-ray crystal-allography (see the Supporting Information).
  • 9
    • 33750466734 scopus 로고    scopus 로고
    • note
    • 4.
  • 10
    • 33750473571 scopus 로고    scopus 로고
    • note
    • Peaks in the crude NMR indicated that decomposition to the furan may be taking place.
  • 15
    • 20544450502 scopus 로고    scopus 로고
    • de Meijere, A., Diederich, F., Eds.; Wiley-VCH: Weinheim, Germany
    • Metal-Catalyzed Cross-Coupling Reactions; de Meijere, A., Diederich, F., Eds.; Wiley-VCH: Weinheim, Germany, 2004.
    • (2004) Metal-Catalyzed Cross-Coupling Reactions
  • 16
    • 33750478846 scopus 로고    scopus 로고
    • note
    • 1H NMR: δ 7.22-7.27 (m, 3H, Ar), 7.09-7.14 (m, 8H, Ar), 6.91-6.99 (m, 4H, Ar), 6.42 (m, 1H, C-2), 5.93 (dd, J = 3.9, 1.2 Hz, 1H, C-3), 5.85 (d, J = 8.1 Hz, 1H, C-5 oxazolidinone), 5.59 (m, 1H, C-5). 5.23 (d, J = 8.1 Hz, 1H, C-4 oxazolidinone), -0.10 (s, 9H, TMS).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.