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Volumn , Issue 3, 1999, Pages 257-258

The enantioselective chalcogeno-Baylis-Hillman reaction using a chiral hydroxy chalcogenide-TiCl4 complex

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EID: 0033246939     PISSN: 03667022     EISSN: None     Source Type: Journal    
DOI: 10.1246/cl.1999.257     Document Type: Article
Times cited : (54)

References (16)
  • 1
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    • D. Basavaiah, P. D. Rao, and R. S. Hyma, Tetrahedron, 52, 8001 (1996); S. E. Drewes and G. H. P. Roos, Tetrahedron, 44, 4653 (1988); E. Ciganek, Org. React., 51, 201 (1997).
    • (1996) Tetrahedron , vol.52 , pp. 8001
    • Basavaiah, D.1    Rao, P.D.2    Hyma, R.S.3
  • 2
    • 4744362831 scopus 로고
    • D. Basavaiah, P. D. Rao, and R. S. Hyma, Tetrahedron, 52, 8001 (1996); S. E. Drewes and G. H. P. Roos, Tetrahedron, 44, 4653 (1988); E. Ciganek, Org. React., 51, 201 (1997).
    • (1988) Tetrahedron , vol.44 , pp. 4653
    • Drewes, S.E.1    Roos, G.H.P.2
  • 3
    • 0342419508 scopus 로고    scopus 로고
    • D. Basavaiah, P. D. Rao, and R. S. Hyma, Tetrahedron, 52, 8001 (1996); S. E. Drewes and G. H. P. Roos, Tetrahedron, 44, 4653 (1988); E. Ciganek, Org. React., 51, 201 (1997).
    • (1997) Org. React. , vol.51 , pp. 201
    • Ciganek, E.1
  • 9
    • 0032564002 scopus 로고    scopus 로고
    • T. Kataoka, T. Iwama, and S. Tsujiyama, Chem. Commun., 1998, 197; T. Kataoka, T. Iwama, S. Tsujiyama, T. Iwamura, and S. Watanabe, Tetrahedron, 54, 11813 (1998).
    • Chem. Commun. , vol.1998 , pp. 197
    • Kataoka, T.1    Iwama, T.2    Tsujiyama, S.3
  • 11
    • 0009200782 scopus 로고    scopus 로고
    • note
    • 4) and evaporated under reduced pressure. The residue was purified by preparative TLC on silica gel eluting with ethyl acetate -hexane (1 : 2, v/v) to give adduct 3.
  • 12
    • 0009195642 scopus 로고    scopus 로고
    • note
    • 4 in EtOH) in DMF.
  • 13
    • 0009266381 scopus 로고    scopus 로고
    • note
    • 4 in EtOH) and MeI in DMF.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.