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Volumn 128, Issue 4, 2006, Pages 1139-1146

In situ generation of vinyl allenes and its applications to one-pot assembly of cyclohexene, cyclooctadiene, 3,7-nonadienone, and bicyclo[6.4.0]dodecene derivatives with palladium-catalyzed multicomponent reactions

Author keywords

[No Author keywords available]

Indexed keywords

ADDITION REACTIONS; CATALYSIS; MOLECULAR DYNAMICS; PALLADIUM; REACTION KINETICS; SYNTHESIS (CHEMICAL);

EID: 31944436823     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja054144v     Document Type: Article
Times cited : (105)

References (61)
  • 5
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    • Vogtle, F., Stoddart, J. F., Shibasaki, M., Eds.; Wiley-VCH: Weinheim, Germany
    • (e) Tietze, L. F.; Haunert, F. Stimulating Concepts in Chemistry; Vogtle, F., Stoddart, J. F., Shibasaki, M., Eds.; Wiley-VCH: Weinheim, Germany, 2000; p 39.
    • (2000) Stimulating Concepts in Chemistry , pp. 39
    • Tietze, L.F.1    Haunert, F.2
  • 12
    • 0027999819 scopus 로고
    • (l) Hall, N. Science 1994, 266, 32.
    • (1994) Science , vol.266 , pp. 32
    • Hall, N.1
  • 23
    • 0034246704 scopus 로고    scopus 로고
    • (d) Yet, L. Chem. Rev. 2000, 100, 2963.
    • (2000) Chem. Rev. , vol.100 , pp. 2963
    • Yet, L.1
  • 25
    • 0000330557 scopus 로고    scopus 로고
    • For reviews on the synthesis of cyclooctanoid systems, see: (a) Mehta, G.; Singh, V. Chem. Rev. 1999, 99, 881.
    • (1999) Chem. Rev. , vol.99 , pp. 881
    • Mehta, G.1    Singh, V.2
  • 55
    • 31944447637 scopus 로고    scopus 로고
    • note
    • Although reaction of the enol triflate of 3-bromoacetophenone with allenylindium produced 6m in 79% yield (DMF, 50 °C, 2 h) via Pd-catalyzed cross-coupling reaction and [4 + 4] cycloaddition, 4-(3-bromophenyl)-1,2,4- pentatriene (10) via Pd-catalyzed cross-coupling reaction was obtained in 70% yield using DMF at 50 °C for 1 h. The fact that 6m is not formed in any amount under these conditions is a confusing observation.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.