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Volumn 8, Issue 19, 1997, Pages 3293-3308

Enantioface-differentiating protonation with chiral γ-hydroxyselenoxides

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOHEXANONE DERIVATIVE; CYCLOPENTANONE DERIVATIVE;

EID: 0030773296     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(97)00423-0     Document Type: Article
Times cited : (50)

References (31)
  • 1
    • 0003905731 scopus 로고
    • Academic Press, New York
    • Reviews: Asymmetric Synthesis, Morrison, J. D. Ed., Academic Press, New York, 1983, vol. 2 and 1984, vol. 3.
    • (1983) Asymmetric Synthesis , vol.2
    • Morrison, J.D.1
  • 2
    • 85070034776 scopus 로고
    • Reviews: Asymmetric Synthesis, Morrison, J. D. Ed., Academic Press, New York, 1983, vol. 2 and 1984, vol. 3.
    • (1984) Asymmetric Synthesis , vol.3
  • 4
    • 0029280768 scopus 로고
    • and references cited therein
    • (b) Komatsu, N.; Uemura, S. Synth. Org. Chem. 1995, 53, 268, and references cited therein.
    • (1995) Synth. Org. Chem. , vol.53 , pp. 268
    • Komatsu, N.1    Uemura, S.2
  • 9
    • 85070037572 scopus 로고    scopus 로고
    • Se)-1a is supported by FT-IR spectra and X-ray crystallography (ref. 5)
    • Se)-1a is supported by FT-IR spectra and X-ray crystallography (ref. 5).
  • 13
    • 0344624517 scopus 로고
    • Wiley, New York Collect
    • House et al. have reported that a directed aldol condensation proceeds in highly stereoselective manner by using a zinc halide enolate: Auerbach, R. A.; Crumrine, D. S.; Ellison, D. L.; House, H. O. in Organic Syntheses, Wiley, New York (1988), Collect. Vol. VI, p. 692.
    • (1988) Organic Syntheses , vol.6 , pp. 692
    • Auerbach, R.A.1    Crumrine, D.S.2    Ellison, D.L.3    House, H.O.4
  • 14
    • 85070033949 scopus 로고    scopus 로고
    • 26=-33.6 (c 0.46, MeOH). Absolute configuration of the major enantiomer of 7b was suggested to be S by comparing the sign of specific rotation with 7a (ref. 9)
    • 26=-33.6 (c 0.46, MeOH). Absolute configuration of the major enantiomer of 7b was suggested to be S by comparing the sign of specific rotation with 7a (ref. 9).
  • 18
    • 33751155033 scopus 로고
    • 25=+15.4 (c 2.1, MeOH) for (R)-7e (9% ee): Ohta, T.; Miyake, T.; Seido, N.; Kumobayashi, H.; Takaya, H. J. Org. Chem. 1995, 60, 357; Chem. Abstr. 1995, 122, 264597g.
    • (1995) Chem. Abstr. , vol.122
  • 22
    • 85070034940 scopus 로고    scopus 로고
    • 3 (0.005 M)
    • 3 (0.005 M).
  • 28
    • 0011830618 scopus 로고
    • Poth, N. Rev. Tech. Luxemb. 1976, 68, 195; Chem. Abstr. 1977, 87, 135965k.
    • (1976) Rev. Tech. Luxemb. , vol.68 , pp. 195
    • Poth, N.1
  • 29
    • 26744441884 scopus 로고
    • Poth, N. Rev. Tech. Luxemb. 1976, 68, 195; Chem. Abstr. 1977, 87, 135965k.
    • (1977) Chem. Abstr. , vol.87


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.