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Volumn 11, Issue 20, 2000, Pages 4153-4162

Synthesis of novel N, P chiral ligands for palladium-catalyzed asymmetric allylations: The effect of binaphthyl backbone on the enantioselectivity

Author keywords

[No Author keywords available]

Indexed keywords

1,1' BINAPHTHYL DERIVATIVE; ALLYL COMPOUND; LIGAND; PHOSPHINE DERIVATIVE;

EID: 0034692891     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(00)00394-3     Document Type: Article
Times cited : (66)

References (12)
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    • (a) Vyskocil, S.; Smrcina, M.; Hanus, V.; Polasek, M.; Kocovsky, P. J. Org. Chem. 1998, 63, 7738-7748. (b) Ding, K.; Wang, Y.; Yun, H.; Liu, J.; Wu, Y.; Terada, M.; Okubo, Y.; Mikami, K. Chem. Eur. J. 1999, 5, 1734-1737
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    • (a) Vyskocil, S.; Smrcina, M.; Kocovsky, P. Tetrahedron Lett. 1998, 39, 9289-9292. (b) Vyskocil, S.; Cisarova, I.; Sejbal, J.; Tislerova, I.; Smrcina, M.; Lloyd-Jones, G. C.; Stephen, S. C.; Butts, C. P.; Murray, M.; Langer, V. J. Am. Chem. Soc. 1999, 121, 7714-7715. © Kocovsky, P.; Malkov, A. V.; Vyskocil, S.; Lloyd-Jones, G. C. Pure Appl. Chem. 1999, 71, 1425-1433
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    • For examples: (a) Zhang, X.; Mashima, K.; Koyano, K.; Sayo, N.; Kumobayashi, H.; Akutagawa, S.; Takaya, H. J. Chem. Soc., Perkin Trans. 1994, 2309-2322. (b) Zhang, X.; Uemura, T.; Matsumura, K.; Sayo, N.; Kumobayashi, H.; Takaya, H. Synlett 1994, 501-503. © Xiao, J.; Nefkens, S. C. A.; Jessop, P. G.; Ikariya, T.; Noyori, R. Tetrahedron Lett. 1996, 37, 2813-2816. (d) Uemura, T.; Zhang, X.; Matsumura, K.; Sayo, N.; Kumobayashi, H.; Ohta, T.; Nozaki, K.; Takaya, H. J. Org. Chem. 1996, 61, 5510-5516. (e) Chan, A. S. C.; Zhang, F.-Y.; Yip, C.-W. J. Am. Chem. Soc. 1997, 119, 4080-4081. (f) Zhang, F.-Y.; Pai, C.-C.; Chan, A. S. C. J. Am. Chem. Soc. 1998, 120, 5808-5809. (g) Zhang, F.-Y.; Yip, C.-W.; Cao, R.; Chan, A. S. C. Tetrahedron: Asymmetry 1997, 8, 585-589
  • 6
    • 84992263305 scopus 로고    scopus 로고
    • Guo, H.; Ding, K. Tetrahedron Lett. 2000, 41, in press
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    • 84992242058 scopus 로고    scopus 로고
    • (a) Guo, H.; Wang, Y.; Ding, K. Chin. J. Chem. 2000, in press. (b) see also Ref. 1e
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    • Imamoto, T.; Takeyama, T.; Kusumoto, T. Chem. Lett. 1985, 1491-1492
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    • For comprehensive reviews, see: (a) Trost, B. M.; Van Vranken, D. L. Chem. Rev. 1996, 96, 395. (b) Heumann, A.; Reglier, M. Tetrahedron 1995, 51, 975-1015. © Hayashi, T. In Catalytic Asymmetric Synthesis; Ojiama, I., Ed.; VCH: New York, 1993; pp. 325-365
  • 10
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    • For examples, see: (a) Deng, W.-P.; Hou, X.-L.; Dai, L.-X.; Yu, Y.-H.; Xia, W. Chem. Commun. 2000, 285-286. (b) Sprinz, J.; Helmchen, G. Tetrahedron Lett. 1993, 34, 1769-1772. © Matt, P. V., Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1993, 32, 566-568. (d) Dawson, G. J.; Frost, C. G.; Williams, J. M. J.; Coote, S. J. Tetrahedron Lett. 1993, 34, 3149-3150. (e) Ogasawara, M.; Yoshida, K.; Kamei, H.; Kato, K.; Uozumi, Y.; Hayashi, T. Tetrahedron: Asymmetry 1998, 9, 1779-1787. (f) Imai, Y.; Zhang, W.; Kida, T.; Nakatsuji, Y.; Ikeda, I. Tetrahedron Lett. 1998, 39, 4343-4346. (g) Selvakumar, K.; Valentini, M.; Woerle, M.; Pregosin, P. S.; Albinati, A. Organometallics 1999, 18, 1207-1215
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    • The best asymmetric induction obtained with MAP was reported to be 71% ee, see Ref. 3a
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    • Hunt, B. B.; Saunders, B. C. J. Chem. Soc. 1957, 2413-2414


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.