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Volumn 53, Issue 15, 1997, Pages 5563-5572

Reductive opening of phenyl substituted thiacycloalkanes: New way for sulphur-containing organolithium compounds

Author keywords

[No Author keywords available]

Indexed keywords

ORGANOLITHIUM COMPOUND; SULFUR;

EID: 0030937729     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(97)00211-1     Document Type: Article
Times cited : (42)

References (31)
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    • See, for instance: Ramón, D. J.; Yus, M. Tetrahedron 1996, 52, 13739-13750, and references cited therein.
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    • Ramón, D.J.1    Yus, M.2
  • 5
    • 0029936158 scopus 로고    scopus 로고
    • and references cited therein
    • See, for instance: Almena, J.; Foubelo, F.; Yus, M. Tetrahedron 1996, 52, 8545-8564, and references cited therein.
    • (1996) Tetrahedron , vol.52 , pp. 8545-8564
    • Almena, J.1    Foubelo, F.2    Yus, M.3
  • 7
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    • (b) For a recent review, see: Yus, M. Chem. Soc. Rev. 1996, 155-161.
    • (1996) Chem. Soc. Rev. , pp. 155-161
    • Yus, M.1
  • 8
    • 0030569283 scopus 로고    scopus 로고
    • (a) For the last paper on this topic from our laboratory, see: Alonso, E.; Ramón, D. J.; Yus, M. Tetrahedron 1996, 52, 14341-14348.
    • (1996) Tetrahedron , vol.52 , pp. 14341-14348
    • Alonso, E.1    Ramón, D.J.2    Yus, M.3
  • 9
    • 0343325694 scopus 로고    scopus 로고
    • For the last paper on this topic from our laboratory, see reference 4
    • (b) For the last paper on this topic from our laboratory, see reference 4.
  • 10
    • 0342890693 scopus 로고    scopus 로고
    • For the last paper on this topic from our laboratory, see reference 5
    • (c) For the last paper on this topic from our laboratory, see reference 5.
  • 11
    • 0030071426 scopus 로고    scopus 로고
    • (d) For the last paper on this topic from our laboratory, see: Guijarro, A.; Yus, M. Tetrahedron. 1996, 52, 1797-1810.
    • (1996) Tetrahedron , vol.52 , pp. 1797-1810
    • Guijarro, A.1    Yus, M.2
  • 15
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    • Phenylthiirane was prepared from styrene oxide by treatment with thiourea: (a) Bordwell, F. G.; Andersen, H. M. J. Am. Chem. Soc. 1953, 75, 4959-4962. For a recent account of this reaction, see:
    • (1953) J. Am. Chem. Soc. , vol.75 , pp. 4959-4962
    • Bordwell, F.G.1    Andersen, H.M.2
  • 19
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    • Obolentsev, R. D.; Bukarov, V. G. Khim. Sera-Org.Soedinenii Soderzhashch. v. Nefti i Nerfte-produkt. 1957, 9-19; Chem. Abstr. 1961, 55, 25908b.
    • (1961) Chem. Abstr. , vol.55
  • 21
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    • Volynskii, N. P.; Gal'pern, G. D.; Smolyanisov, V. V. Neftekhimiya 1963, 3, 482-487; Chem. Abstr. 1963, 59, 11410a.
    • (1963) Chem. Abstr. , vol.59
  • 22
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    • ω-Chloro propio and butyro phenones are commercially available. 5-Chlorovalerophenone (Wilt, J. W.; Hill, J. W. J. Org. Chem. 1961, 26, 3523-3525) was prepared by Friedel-Crafts acylation of benzene with 5-chlorovaleryl chloride.
    • (1961) J. Org. Chem. , vol.26 , pp. 3523-3525
    • Wilt, J.W.1    Hill, J.W.2
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    • Ph. D. University of Oviedo, p. 118
    • (b) Florez, J. Ph. D. 1984, University of Oviedo, p. 118.
    • (1984)
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    • Schaal, C. Bull. Soc. Chim. Fr. 1971, 3064-3070; Chem. Abstr. 1971, 75, 129221a.
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  • 31
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    • For products 3b-d, 6b-d, 9c-g, was not possible to obtain the corresponding HRMS due to the low intensity or the absence of the M+ signal
    • For products 3b-d, 6b-d, 9c-g, was not possible to obtain the corresponding HRMS due to the low intensity or the absence of the M+ signal.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.