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Volumn 21, Issue 20, 2002, Pages 4275-4280

Chelating diphosphines that contain a rhenium stereocenter in the backbone: Applications in rhodium-catalyzed enantioselective ketone hydrosilylations and alkene hydrogenations

Author keywords

[No Author keywords available]

Indexed keywords

HYDROSILYLATIONS;

EID: 0001610167     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om020432d     Document Type: Article
Times cited : (50)

References (67)
  • 1
    • 0037553445 scopus 로고    scopus 로고
    • Jacobsen, E. N., Pfaltz, A., Yamamoto, H. Eds.; Springer: Berlin, Germany, Chapter 6.3.
    • (a) Nishiyama, H. In Comprehensive Asymmetric Catalysis I-III; Jacobsen, E. N., Pfaltz, A., Yamamoto, H. Eds.; Springer: Berlin, Germany, 1999; Chapter 6.3.
    • (1999) Comprehensive Asymmetric Catalysis I-III
    • Nishiyama, H.1
  • 3
    • 0033597622 scopus 로고    scopus 로고
    • Some full papers that have appeared since the preceding reviews: (a) Yun, J.; Buchwald, S. L. J. Am. Chem. Soc. 1999, 121, 5640.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 5640
    • Yun, J.1    Buchwald, S.L.2
  • 11
    • 0035742298 scopus 로고    scopus 로고
    • For an essay on the unattainable limit of an "ideal catalyst", see: Gladysz, J. A. Pure Appl. Chem. 2001, 73, 1319.
    • (2001) Pure Appl. Chem. , vol.73 , pp. 1319
    • Gladysz, J.A.1
  • 13
    • 0000380332 scopus 로고    scopus 로고
    • Recent reviews are cited in ref 12. For commercial applications, see the following, (a) Dobbs, D. A.; Vanhessche, K. P. M.; Brazi, E.; Rautenstrauch, V.; Lenoir, J.-Y.; Genèt, J.-P.; Wiles, J.; Bergens, S. H. Angew. Chem., Int. Ed. 2000, 39, 1992; Angew. Chem. 2000, 112, 2080.
    • (2000) Angew. Chem. , vol.112 , pp. 2080
  • 16
    • 33748225871 scopus 로고
    • (a) Sawamura, M.; Kuwano, R.; Ito, Y. Angew. Chem., Int. Ed. Engl. 1994, 33, 111; Angew. Chem. 1994, 106, 92.
    • (1994) Angew. Chem. , vol.106 , pp. 92
  • 33
    • 0023537030 scopus 로고
    • Preliminary communication of some of the work in the preceding paper: Zwick, B. D.; Arif, A. M.; Patton, A. T.; Gladysz, J. A. Angew. Chem., Int. Ed. Engl. 1987, 26, 910; Angew. Chem. 1987, 99, 921.
    • (1987) Angew. Chem. , vol.99 , pp. 921
  • 36
    • 0038567620 scopus 로고    scopus 로고
    • note
    • c)-7 as given elsewhere).
  • 39
    • 0032538768 scopus 로고    scopus 로고
    • Selected recent references: (a) Kudis, S.; Helmchen, G. Angew. Chem., Int. Ed. 1998, 37, 3047; Angew. Chem. 1998, 110, 3210.
    • (1998) Angew. Chem. , vol.110 , pp. 3210
  • 44
    • 0035901665 scopus 로고    scopus 로고
    • (e) Bolm, C.; Kesselgruber, M.; Hermanns, N.; Hildebrand, J. P,; Raabe, G. Angew. Chem., Int. Ed. 2001, 40, 1488; Angew. Chem. 2001, 113, 1536.
    • (2001) Angew. Chem. , vol.113 , pp. 1536
  • 49
    • 0037553441 scopus 로고    scopus 로고
    • note
    • (b) The abbreviations "DH" (degree of hydrosilylation, corresponding to total conversion to 10 and 11) and "CY" (chemical yield, corresponding to conversion to 10) are often used.
  • 50
    • 0012706264 scopus 로고
    • Literature NMR data are as follows. 10a and 11a: ref 16a. 10a,b: ref 16b. 11c: Ojima, I.; Kogure, T. Organometallics 1982, 1, 1390. The silyl ether 10d and alcohol 12d are reported in ref 6d.
    • (1982) Organometallics , vol.1 , pp. 1390
    • Ojima, I.1    Kogure, T.2
  • 52
    • 0038228841 scopus 로고    scopus 로고
    • note
    • 6d is provisional and based upon (1) the order of chromatographic elution and (2) the dominant enantiomer obtained for 12a-c.
  • 53
  • 57
    • 0035905563 scopus 로고    scopus 로고
    • (a) Rossen, K. Angew. Chem., Int. Ed. 2001, 40, 4611; Angew. Chem. 2001, 113, 4747.
    • (2001) Angew. Chem. , vol.113 , pp. 4747
  • 63
    • 0037012673 scopus 로고    scopus 로고
    • and references therein
    • Tang, W.; Zhang, X. Angew. Chem., Int. Ed. 2002, 41, 1612; Angew. Chem. 2002, 114, 1682 and references therein.
    • (2002) Angew. Chem. , vol.114 , pp. 1682
  • 65
    • 0037891388 scopus 로고    scopus 로고
    • note
    • 2).
  • 67
    • 0038567618 scopus 로고    scopus 로고
    • note
    • The solvent was removed under vacuum, the residue was extracted with ether, and the extract was filtered through a silica gel plug. The solvent was removed from the filtrate, the residue extracted with ether (14a) or methanol (14b), and the extract passed through a syringe filter.


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