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Volumn 64, Issue 11, 1999, Pages 3996-4004

Phosphorus-chiral analogues of 1,1'-bis(diphenylphosphino)ferrocene: Asymmetric synthesis and application in highly enantioselective rhodium- catalyzed hydrogenation reactions

Author keywords

[No Author keywords available]

Indexed keywords

1,1' BIS(1 NAPHTHYLPHENYLPHOSPHINO)FERROCENE; 1,1' BIS(2 BIPHENYLPHENYLPHOSPHINO)FERROCENE; 1,1' BIS(2 NAPHTHYLPHENYLPHOSPHINO)FERROCENE; 1,1' BIS(9 PHENANTHRYLPHENYLPHOSPHINO)FERROCENE; 1,1' BIS(DIPHENYLPHOSPHINO)FERROCENE; 1,1' BIS[(2 METHOXYPHENYL)PHENYLPHOSPHINO]FERROCENE; ALPHA (ACYLAMINO)CINNAMIC ACID DERIVATIVE; FERROCENE DERIVATIVE; RHODIUM; UNCLASSIFIED DRUG;

EID: 0033612232     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo982481z     Document Type: Article
Times cited : (80)

References (48)
  • 1
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    • For representative reviews, see, for example: (a) Noyori R. Asymmetric Catalysis in Organic Synthesis; John Wiley: New York, 1994. (b) Ojima, I., Ed. Catalytic Asymmetric Synthesis; VCH Publishers: Weinheim, 1993.
    • (1994) Asymmetric Catalysis in Organic Synthesis
  • 2
    • 0003544583 scopus 로고
    • VCH Publishers: Weinheim
    • For representative reviews, see, for example: (a) Noyori R. Asymmetric Catalysis in Organic Synthesis; John Wiley: New York, 1994. (b) Ojima, I., Ed. Catalytic Asymmetric Synthesis; VCH Publishers: Weinheim, 1993.
    • (1993) Catalytic Asymmetric Synthesis
    • Ojima, I.1
  • 18
    • 0004221233 scopus 로고
    • Togni, A.; Hayashi, T., Eds.; VCH Publishers: Weinheim
    • (a) Gan, K.-S.; Hor, T. S. A. In Ferrocenes; Togni, A.; Hayashi, T., Eds.; VCH Publishers: Weinheim, 1995.
    • (1995) Ferrocenes
    • Gan, K.-S.1    Hor, T.S.A.2
  • 19
    • 0032541093 scopus 로고    scopus 로고
    • and references therein
    • (b) For examples of nonracemic ferrocene derivatives applied in asymmetric synthesis, see: Richards, C. J.; Locke, A. J. Tetrahedron: Asymmetry 1998, 9, 2377 and references therein.
    • (1998) Tetrahedron: Asymmetry , vol.9 , pp. 2377
    • Richards, C.J.1    Locke, A.J.2
  • 20
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    • note
    • (a) Compounds 4a, 4c, 5a, and 5c were first described in ref 12.
  • 26
    • 0344240794 scopus 로고    scopus 로고
    • These findings are in agreement with previously made observations; see ref 14b
    • These findings are in agreement with previously made observations; see ref 14b.
  • 27
    • 0001626461 scopus 로고
    • The deboronation step is reported to proceed without loss of enantiomeric purity: Imamoto, T.; Oshiki, T.; Onozawa, T.; Kusumoto, T.; Sato, K. J. Am. Chem. Soc. 1990, 112, 5244. Stirring at reflux temperature for longer reaction times, however, has been observed to cause minor racemization: ref 14c.
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 5244
    • Imamoto, T.1    Oshiki, T.2    Onozawa, T.3    Kusumoto, T.4    Sato, K.5
  • 32
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    • Morrison, J. D., Ed.; Academic Press: New York
    • (a) For a review on asymmetric hydrogenation of α-(N-acylamino)acrylic acid derivatives, see: Koenig, K. E. In Asymmetric Synthesis; Morrison, J. D., Ed.; Academic Press: New York, 1985; Vol. 5.
    • (1985) Asymmetric Synthesis , vol.5
    • Koenig, K.E.1
  • 48
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    • Miyashita, A.; Takaya, H.; Souchi, T.; Noyori, R. Tetrahedron 1984, 40, 1245. Characterization data for hydrogenation products were found to be identical to those of authentic samples.
    • (1984) Tetrahedron , vol.40 , pp. 1245
    • Miyashita, A.1    Takaya, H.2    Souchi, T.3    Noyori, R.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.