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Volumn 32, Issue 2, 2013, Pages 623-635

Synthesis, molecular structure, and catalytic evaluation of centrostereogenic ferrocenophane phosphines

Author keywords

[No Author keywords available]

Indexed keywords

AS-LIGANDS; ASYMMETRIC ALLYLIC ALKYLATIONS; CATALYTIC EVALUATION; CATALYTIC REACTIONS; CHIRAL ALCOHOLS; CHLOROTRIMETHYLSILANES; DIMETHYL MALONATE; ENANTIOSELECTIVE; FERROCENES; FERROCENOPHANES; METHYL VINYL KETONES; PALLADIUM COMPLEXES; SODIUM IODIDES; TRIFLUOROMETHYL;

EID: 84872977810     PISSN: 02767333     EISSN: 15206041     Source Type: Journal    
DOI: 10.1021/om3011245     Document Type: Article
Times cited : (21)

References (102)
  • 3
    • 0000126044 scopus 로고    scopus 로고
    • Togni, A. Halterman, R. L. Wiley-VCH: Weinheim, Germany, Chapter 11
    • Togni, A. In Metallocenes: Synthesis, Reactivity, Applications; Togni, A., Halterman, R. L., Eds.; Wiley-VCH: Weinheim, Germany, 1998; Vol. 2, Chapter 11, pp 685-721.
    • (1998) Metallocenes: Synthesis, Reactivity, Applications , vol.2 , pp. 685-721
    • Togni, A.1
  • 56
    • 0003203028 scopus 로고
    • 13C NMR of Transition Metal Phosphane Complexes.
    • Diehl, P. Fluck, E. Kosfeld, R. Springer: Berlin, Vol. chapter E, p. ff and references therein.
    • 13C NMR of Transition Metal Phosphane Complexes. In NMR Basic Principles and Progress; Diehl, P.; Fluck, E.; Kosfeld, R., Eds.; Springer: Berlin, 1979; Vol. 16, chapter E, p. 65 ff and references therein.
    • (1979) NMR Basic Principles and Progress , vol.16 , pp. 65
    • Pregosin, P.S.1    Kunz, R.W.2
  • 73
    • 0002795445 scopus 로고
    • Ojima, I. VCH: New York, Chapter 7.1
    • Hayashi, T. In Catalytic Asymmetric Synthesis; Ojima, I., Ed.; VCH: New York, 1993; Chapter 7.1, pp 325-365.
    • (1993) Catalytic Asymmetric Synthesis , pp. 325-365
    • Hayashi, T.1
  • 84
    • 84872962043 scopus 로고
    • Chem. Abstr. 1972, 77, 34147q.
    • (1972) Chem. Abstr. , vol.77
  • 96
    • 1942521263 scopus 로고    scopus 로고
    • Acetate 6 was prepared by acylation of the commercially available racemic 1,3-diphenylprop-2-en-1-ol as described in the literature
    • Acetate 6 was prepared by acylation of the commercially available racemic 1,3-diphenylprop-2-en-1-ol as described in the literature: Watson, I. D. G.; Styler, S. A.; Yudin, A. K. J. Am. Chem. Soc. 2004, 126, 5086
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 5086
    • Watson, I.D.G.1    Styler, S.A.2    Yudin, A.K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.