메뉴 건너뛰기




Volumn 465, Issue 1-2, 1994, Pages 85-92

Palladium-catalyzed cross-coupling of aryl and alkenyl boronic acids with alkenes via oxidative addition of a carbonboron bond to palladium(O)

Author keywords

Alkene; Alkenyl; Aryl; Boronic acid; Oxidative addition; Palladium

Indexed keywords


EID: 0001918453     PISSN: 0022328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/0022-328X(94)87040-3     Document Type: Article
Times cited : (139)

References (50)
  • 13
    • 85039397112 scopus 로고
    • Synthesis of Sterically Hindered Biaryls via the Palladium-Catalyzed Cross-Coupling Reaction of Arylboronic Acids or their Esters with Haloarenes
    • (1992) Synlett , pp. 207
    • Watanabe1    Miyaura2    Suzuki3
  • 14
    • 84914026541 scopus 로고
    • Palladium-Catalyzed Cross-Coupling Reactions in a Homogeneous Aqueous Medium
    • (1992) Synlett , pp. 715
    • Genet1    Blart2    Savignac3
  • 28
    • 84913006646 scopus 로고    scopus 로고
    • Presented at the 39th Symposium on Organometallic Chemistry, Japan, Tokyo, Oct. 1992; Abstracts p. 445-447
  • 35
    • 0000634286 scopus 로고
    • Pergamon Press, New York, We also confirmed separately that the stirring of 9a in acetic acid gave styrene almost quantitatively either at 25°C for 20 h or at 50°C for 4 h.
    • (1982) Comprehensive Organometallic Chemistry , vol.7 , pp. 305
  • 37
    • 84912963503 scopus 로고    scopus 로고
    • 4 (5 mol%) in acetic acid at 85°C for 5 h afforded 12% yield of trans-stilbene together with 2% yield of biphenyl.
  • 41
    • 84913013326 scopus 로고    scopus 로고
    • 4 (1 mmol) in AcOH (10 ml) at 25°C for 20 h, 2.34 mmol of benzene was obtained.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.