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Volumn , Issue 16, 2000, Pages 2939-2945

Copper(II)-bisoxazoline-catalysed asymmetric Diels-Alder reactions of α-thioacrylates

Author keywords

Asymme tric catalysis; Bisoxazolines; Copper; Cycloadditions; Phenylthioacrylates

Indexed keywords

ACRYLIC ACID DERIVATIVE; COPPER COMPLEX; CYCLOPENTADIENE DERIVATIVE; OXAZOLINE DERIVATIVE;

EID: 0002176525     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/1099-0690(200008)2000:16<2939::AID-EJOC2939>3.0.CO;2-K     Document Type: Article
Times cited : (34)

References (41)
  • 17
    • 6744263518 scopus 로고    scopus 로고
    • note
    • Other bisoxazolines tested include R = iBu and Bn. These gave low enantioselectivities at 0 °C (13% and 7%, respectively) and were not tested further at low temperatures.
  • 18
    • 37049073390 scopus 로고
    • [11]) were prepared from the corresponding sulfoxides by a Pummerer reaction. See: J. Durman, J. I. Grayson, P. G. Hunt, S. Warren, J. Chem. Soc., Perkin Trans. 1 1986, 1939-1945; H. J. Monteiro, A. L. Gemal, Synthesis 1975, 437. Details of the synthesis of trifluoroethyl acrylate 6 are presented in the experimental section.
    • (1986) J. Chem. Soc., Perkin Trans. 1 , pp. 1939-1945
    • Durman, J.1    Grayson, J.I.2    Hunt, P.G.3    Warren, S.4
  • 19
    • 84987524118 scopus 로고
    • [11]) were prepared from the corresponding sulfoxides by a Pummerer reaction. See: J. Durman, J. I. Grayson, P. G. Hunt, S. Warren, J. Chem. Soc., Perkin Trans. 1 1986, 1939-1945; H. J. Monteiro, A. L. Gemal, Synthesis 1975, 437. Details of the synthesis of trifluoroethyl acrylate 6 are presented in the experimental section.
    • (1975) Synthesis , pp. 437
    • Monteiro, H.J.1    Gemal, A.L.2
  • 29
    • 33748939157 scopus 로고
    • For further discussion on the effect of geminal substituents on bite angle see: R. M. Beesley, C. K. Ingold, J. F. Thorpe, J. Chem. Soc., 1915, 107, 1080; M. E. Jung, Synlett, 1999, 843.
    • (1915) J. Chem. Soc. , vol.107 , pp. 1080
    • Beesley, R.M.1    Ingold, C.K.2    Thorpe, J.F.3
  • 30
    • 0033011059 scopus 로고    scopus 로고
    • For further discussion on the effect of geminal substituents on bite angle see: R. M. Beesley, C. K. Ingold, J. F. Thorpe, J. Chem. Soc., 1915, 107, 1080; M. E. Jung, Synlett, 1999, 843.
    • (1999) Synlett , pp. 843
    • Jung, M.E.1
  • 38
    • 84985635661 scopus 로고
    • E. J. Corey, T.-P. Loh, J. Am. Chem. Soc. 1991, 113, 8966. See also: A. E. Greene, C. L. Drian, J. Am. Chem. Soc. 1982, 104, 5473.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 8966
    • Corey, E.J.1    Loh, T.-P.2
  • 39
    • 0000513405 scopus 로고
    • E. J. Corey, T.-P. Loh, J. Am. Chem. Soc. 1991, 113, 8966. See also: A. E. Greene, C. L. Drian, J. Am. Chem. Soc. 1982, 104, 5473.
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 5473
    • Greene, A.E.1    Drian, C.L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.