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Volumn 54, Issue 26, 1998, Pages 7301-7334

Chiral sulfur-containing 1,2-disubstituted ferrocenes

Author keywords

[No Author keywords available]

Indexed keywords

FERROCENE DERIVATIVE;

EID: 0032565909     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(98)00397-4     Document Type: Article
Times cited : (43)

References (59)
  • 1
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    • Ferrocenes, homogeneous catalysis. Organic synthesis
    • Togni, A.; Hayashi T., Eds.: VCH, Weinheim
    • 1. For a recent review, see: Ferrocenes, Homogeneous Catalysis. Organic Synthesis. Materials Science: Togni, A.; Hayashi T., Eds.: VCH, Weinheim, 1995.
    • (1995) Materials Science
  • 2
    • 0001469720 scopus 로고    scopus 로고
    • Hassner, A. Ed.: JAI Press Inc.: Greenwich, Connecticut
    • 2. For a recent review, see: Kagan, H. B.; Riant, O. in "Advances in Asymmetric Synthesis": Hassner, A. Ed.: JAI Press Inc.: Greenwich, Connecticut, 1997; Vol 2, pp. 189-235.
    • (1997) Advances in Asymmetric Synthesis , vol.2 , pp. 189-235
    • Kagan, H.B.1    Riant, O.2
  • 3
    • 84942799202 scopus 로고
    • Wilkinson, G.; Stone, F.G.A., Eds.: Pergamon, Oxford
    • 3. (a) Kagan, H. B. Comprehensive Organometallic Chemistry; Wilkinson, G.; Stone, F.G.A., Eds.: Pergamon, Oxford, 1982, Vol. 8.
    • (1982) Comprehensive Organometallic Chemistry , vol.8
    • Kagan, H.B.1
  • 10
  • 18
    • 0001425763 scopus 로고
    • and references cited therein
    • (b) James, B. R.; McMillan, R. S. Can. J. Chem. 1977, 55, 3927-3932, and references cited therein,
    • (1977) Can. J. Chem. , vol.55 , pp. 3927-3932
    • James, B.R.1    McMillan, R.S.2
  • 31
    • 0002687008 scopus 로고
    • Oae, S., Ed.; Tokyo
    • 11. Transition-metal complexes containing sulfoxides: For a review, see: (a) Kagan, H. B.; Ronan, B. Reviews on Heteroatom Chemistry; Oae, S., Ed.; Tokyo, 1992; pp. 92-116.
    • (1992) Reviews on Heteroatom Chemistry , pp. 92-116
    • Kagan, H.B.1    Ronan, B.2
  • 36
  • 42
    • 50549178839 scopus 로고
    • 13. The nucleophilic substitution of 2S occurs with inversion of configuration at the sulfur center: Andersen, K. K. Tetrahedron Lett. 1962, 93-96.
    • (1962) Tetrahedron Lett. , pp. 93-96
    • Andersen, K.K.1
  • 44
    • 0010480726 scopus 로고    scopus 로고
    • Part of the racemized product may result from the reaction of lithiated ferrocene with 2R which derived from the displacement reaction of lithiated l-menthol with 2S. Although, this displacement reaction takes place slowly under the reaction conditions (at -78 °C)
    • 15. Part of the racemized product may result from the reaction of lithiated ferrocene with 2R which derived from the displacement reaction of lithiated l-menthol with 2S. Although, this displacement reaction takes place slowly under the reaction conditions (at -78 °C).
  • 46
    • 0001779092 scopus 로고
    • 17. The prechelation of sulfoxide with Lewis acid had been reported: (a) Posner, G. H. Acc. Chem. Res. 1987, 20, 72-78.
    • (1987) Acc. Chem. Res. , vol.20 , pp. 72-78
    • Posner, G.H.1
  • 48
    • 0010476325 scopus 로고    scopus 로고
    • The author has deposited atomic coordinates for this structure with the Cambridge Crystallographic Data Centre. The coordinates can be obtained, on request, from the Director, Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge, CB2 1EZ, UK
    • 18. The author has deposited atomic coordinates for this structure with the Cambridge Crystallographic Data Centre. The coordinates can be obtained, on request, from the Director, Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge, CB2 1EZ, UK.
  • 55
    • 33845375398 scopus 로고
    • Prepared by a method similar to that of 1-bromo-2,4,6-trimethylbenzene
    • 22. (a) Bonini, B. F.; Grossi, L.; Lunazzi, L.; Macciantelli, D. J. Org. Chem. 1986, 51, 517-. Prepared by a method similar to that of 1-bromo-2,4,6-trimethylbenzene:
    • (1986) J. Org. Chem. , vol.51 , pp. 517
    • Bonini, B.F.1    Grossi, L.2    Lunazzi, L.3    Macciantelli, D.4
  • 56
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    • Wiley: New York, Collect
    • (b) Smith, L. I. Organic Synthesis; Wiley: New York, 1943; Collect. Vol. II, p95.
    • (1943) Organic Synthesis , vol.2 , pp. 95
    • Smith, L.I.1
  • 58
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    • 24. Compound 38 has been synthesized previously by other methods: (a) Jager, V.; Gunther, H. J. Tetrahedron Lett. 1977, 29, 2543-2546.
    • (1977) Tetrahedron Lett. , vol.29 , pp. 2543-2546
    • Jager, V.1    Gunther, H.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.