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Volumn 52, Issue 31, 1996, Pages 10525-10546

Asymmetric approaches to cyclopentenones in the Ni(0)-promoted cyclocarbonylation reaction of allyl halides and acetylenes

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOPENTENONE DERIVATIVE;

EID: 0141466569     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4020(96)00573-X     Document Type: Article
Times cited : (31)

References (30)
  • 7
    • 5244335075 scopus 로고
    • 2+ catalyzed Michael-type addition of MeOH to 2 followed by sulfoxide elimination. For a related process, see Trost, B.M.; Shi, Y. J. Am. Chem. Soc., 1993, 115, 9421-9438.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 9421-9438
    • Trost, B.M.1    Shi, Y.2
  • 11
    • 85030206386 scopus 로고    scopus 로고
    • Formation of 13 can be interpreted similarly to that of 4 (see ref. 7). Moreover, formation of 13 was observed after treatment of 9a with HCl-MeOH at room temperature
    • 11. Formation of 13 can be interpreted similarly to that of 4 (see ref. 7). Moreover, formation of 13 was observed after treatment of 9a with HCl-MeOH at room temperature.
  • 12
    • 0002745629 scopus 로고
    • Patai, S., Rappoport, Z., Stirling, C., Eds.; John Wiley & Sons: Chichester-New York-Brisbane-Toronto-Singapore
    • 12. Grossert, J. S. In The Chemistry of Sulfones and Sulfoxides; Patai, S., Rappoport, Z., Stirling, C., Eds.; John Wiley & Sons: Chichester-New York-Brisbane-Toronto-Singapore, 1988, p 925-968.
    • (1988) The Chemistry of Sulfones and Sulfoxides , pp. 925-968
    • Grossert, J.S.1
  • 18
    • 85030205152 scopus 로고    scopus 로고
    • PC MODEL, Serena Software, Bloomington, IN
    • 18. PC MODEL, Serena Software, Bloomington, IN.
  • 19
    • 0003544583 scopus 로고
    • Ojima, I., Ed.; VCH Publishers: New York, Weinheim, Cambridge
    • 19. Catalytic Asymmetric Synthesis; Ojima, I., Ed.; VCH Publishers: New York, Weinheim, Cambridge, 1993.
    • (1993) Catalytic Asymmetric Synthesis


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.