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Volumn 7, Issue 14, 2005, Pages 3119-3121

Enantioselective synthesis of axially chiral biaryls through rhodium-catalyzed complete intermolecular cross-cyclotrimerization of internal alkynes

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EID: 22244484424     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0511880     Document Type: Article
Times cited : (90)

References (41)
  • 3
    • 0000332467 scopus 로고
    • Helmchen, G., Hoffmann, R. W., Mulzer, J., Schaumann, E., Eds.; Thieme: Stuttgart
    • Synthesis of axially chiral biaryls using stoichiometric chiral auxiliaries or chiral starting materials: (a) Bringmann, G.; Walter, R.; Weirich, R. In Methods of Organic Chemistry (Hauben Weyl), 4th ed.; Helmchen, G., Hoffmann, R. W., Mulzer, J., Schaumann, E., Eds.; Thieme: Stuttgart, 1995; Vol. E21a, p 567.
    • (1995) Methods of Organic Chemistry (Hauben Weyl), 4th Ed. , vol.E21A , pp. 567
    • Bringmann, G.1    Walter, R.2    Weirich, R.3
  • 14
    • 0033105330 scopus 로고    scopus 로고
    • Cross-coupling of biaryl ditriflates: (j) Kamikawa, T.; Hayashi, T. Tetrahedron 1999, 55, 3455-3466.
    • (1999) Tetrahedron , vol.55 , pp. 3455-3466
    • Kamikawa, T.1    Hayashi, T.2
  • 28
    • 0002110351 scopus 로고    scopus 로고
    • (b) Lautens, M.; Klute, W.; Tam, W. Chem. Rev. 1996, 96, 49-92. Catalytic complete intermolecular cross cyclotrimerization of alkynes.
    • (1996) Chem. Rev. , vol.96 , pp. 49-92
    • Lautens, M.1    Klute, W.2    Tam, W.3
  • 41
    • 32744460758 scopus 로고    scopus 로고
    • note
    • Indeed, in the cross cyclotrimerization shown in Table 3, starting materials 2 and homo-cyclotrimerization products of 1 were isolated other than the desired cross-cyclotrimerization products.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.