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Volumn 65, Issue 11, 2007, Pages 1060-1069

P-chiral phosphine ligands for transition - Metal - Catalyzed asymmetric reactions

Author keywords

[No Author keywords available]

Indexed keywords

ENANTIOSELECTIVITY; HYDROGENATION; MOLECULAR STRUCTURE; PHOSPHORUS;

EID: 38949196759     PISSN: 00379980     EISSN: None     Source Type: Journal    
DOI: 10.5059/yukigoseikyokaishi.65.1060     Document Type: Article
Times cited : (21)

References (83)
  • 1
    • 0003400107 scopus 로고
    • For representative reviews and accounts, see: a, John Wiley & Sons: New York
    • For representative reviews and accounts, see: (a) Noyori, R. Asymmetric Catalysis in Organic Chemistry; John Wiley & Sons: New York, 1994.
    • (1994) Asymmetric Catalysis in Organic Chemistry
    • Noyori, R.1
  • 3
    • 0003445429 scopus 로고    scopus 로고
    • Jacobsen, E. N, Pfaltz, A, Yamamoto, H. Eds, Springer, Berlin
    • (c) Comprehensive Asymmetric Catalysis, I, II, III, Jacobsen, E. N.; Pfaltz, A.; Yamamoto, H. Eds.: Springer, Berlin, 1999.
    • (1999) Comprehensive Asymmetric Catalysis, I, II, III
  • 7
    • 0043240879 scopus 로고    scopus 로고
    • For representative reviews and accounts, see: a
    • For representative reviews and accounts, see: (a) Tang, W.; Zhang, X. Chem. Rev. 2003, 103, 3029.
    • (2003) Chem. Rev , vol.103 , pp. 3029
    • Tang, W.1    Zhang, X.2
  • 21
    • 0000101704 scopus 로고
    • Morrison, J. D, Scott, J. W, Eds, Academic Press: New York, Chapter 3
    • (c) Valentine, D., Jr. In Asymmetric Synthesis; Morrison, J. D.; Scott, J. W., Eds.; Academic Press: New York, 1984; Vol. 4, Chapter 3.
    • (1984) Asymmetric Synthesis , vol.4
    • Valentine Jr., D.1
  • 38
    • 0037459849 scopus 로고    scopus 로고
    • 4). The phosphonium salt is stable in air and can be conveniently used for the asymmetric hydrogenation of enamides and related substrates. Danjo, H.; Sasaki, W.; Miyazaki, T.; Imamoto, T. Tetrahedron Lett. 2003, 44, 3467.
    • 4). The phosphonium salt is stable in air and can be conveniently used for the asymmetric hydrogenation of enamides and related substrates. Danjo, H.; Sasaki, W.; Miyazaki, T.; Imamoto, T. Tetrahedron Lett. 2003, 44, 3467.
  • 40
    • 85036978486 scopus 로고    scopus 로고
    • 4 are available from Tokyo Chemical Industry Co., Ltd.
    • 4 are available from Tokyo Chemical Industry Co., Ltd.
  • 43
    • 85036959439 scopus 로고    scopus 로고
    • Burk and co-workers previously observed this dramatic difference in the stereochemical outcome of the asymmetric hydrogenation of enamides with (S,S)-Me-DuPHOS catalyst. Burk, M. J, Casy, G, Johnson, N. B. J. Org. Chem. 1998, 63, 6084
    • Burk and co-workers previously observed this dramatic difference in the stereochemical outcome of the asymmetric hydrogenation of enamides with (S,S)-Me-DuPHOS catalyst. Burk, M. J.; Casy, G.; Johnson, N. B. J. Org. Chem. 1998, 63, 6084.
  • 49
    • 0035809275 scopus 로고    scopus 로고
    • -, see: Gridnev, I. D.; Imamoto, T. Organometallics 2001, 20, 545.
    • -, see: Gridnev, I. D.; Imamoto, T. Organometallics 2001, 20, 545.
  • 53
    • 85036959990 scopus 로고    scopus 로고
    • May 3, 25
    • Chem. Eng. News 2004, May 3, 25.
    • (2004) Chem. Eng. News
  • 54
    • 33746345331 scopus 로고    scopus 로고
    • O'Brien and co-workers reported a novel method for the preparation of P-stereogenic bisphosphines by the use of catalytic amounts of chiral diamines. Genet, C.; Canipa, S. J.; O'Brien, P.; Taylor, S. J. Am. Chem. Soc. 2006, 128, 9336.
    • O'Brien and co-workers reported a novel method for the preparation of P-stereogenic bisphosphines by the use of catalytic amounts of chiral diamines. Genet, C.; Canipa, S. J.; O'Brien, P.; Taylor, S. J. Am. Chem. Soc. 2006, 128, 9336.
  • 79
    • 85036986299 scopus 로고    scopus 로고
    • This ligand is prepared on a large scale by Nippon Chemical Industrial Co. Ltd. and is commercialized by Sigma-Aldrich
    • This ligand is prepared on a large scale by Nippon Chemical Industrial Co. Ltd. and is commercialized by Sigma-Aldrich.
  • 83
    • 4644299461 scopus 로고    scopus 로고
    • Gridnev, I. D.; Imamoto, T. Acc. Chem. Res. 2004, 37, 633, and references 18, 19, 21, 22, 26, and 27.
    • (c) Gridnev, I. D.; Imamoto, T. Acc. Chem. Res. 2004, 37, 633, and references 18, 19, 21, 22, 26, and 27.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.