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Volumn 36, Issue 3, 1997, Pages 235-236

Enantioselective Hydrogen Transfer from a Chiral Tin Hydride to a Prochiral Carbon-Centered Radical

Author keywords

Asymmetric synthesis; Homogeneous catalysis; Radicals; Tin

Indexed keywords


EID: 0030935083     PISSN: 05700833     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.199702351     Document Type: Article
Times cited : (70)

References (24)
  • 8
    • 48749136090 scopus 로고
    • Schumann et al. reported the enantioselective reduction of tertiary alkyl halides with chiral diorganoalkoxytin hydrides: H. Schumann, B. Pachaly, B. C. Schütze, J. Organomet. Chem. 1984, 265, 145-152.
    • (1984) J. Organomet. Chem. , vol.265 , pp. 145-152
    • Schumann, H.1    Pachaly, B.2    Schütze, B.C.3
  • 9
    • 0001214485 scopus 로고
    • Tin hydrides in which tin is the only chiral center undergo racemization when exposed to radical chain reaction conditions: a) M. Gielen, Y. Tondeur, J. Organomet. Chem. 1979, 169, 265-281; b) M. Gielen, Pure Appl. Chem. 1980, 52, 657-667.
    • (1979) J. Organomet. Chem. , vol.169 , pp. 265-281
    • Gielen, M.1    Tondeur, Y.2
  • 10
    • 0642382533 scopus 로고
    • Tin hydrides in which tin is the only chiral center undergo racemization when exposed to radical chain reaction conditions: a) M. Gielen, Y. Tondeur, J. Organomet. Chem. 1979, 169, 265-281; b) M. Gielen, Pure Appl. Chem. 1980, 52, 657-667.
    • (1980) Pure Appl. Chem. , vol.52 , pp. 657-667
    • Gielen, M.1
  • 13
    • 37049072213 scopus 로고
    • and references therein
    • Enantioselective abstractions of hydrogen atoms from chiral, racemic substrates by chiral radicals have been reported: H.-S. Dang, V. Diart, B. P. Roberts, D. A. Tocher, J. Chem. Soc. Perkin Trans. 2 1994, 1039-1045, and references therein.
    • (1994) J. Chem. Soc. Perkin Trans. 2 , pp. 1039-1045
    • Dang, H.-S.1    Diart, V.2    Roberts, B.P.3    Tocher, D.A.4
  • 15
    • 0642321119 scopus 로고    scopus 로고
    • Jpn. Kokai Tokkyo Koho JP 04 91,093, 1992
    • b) R. Noyori, M. Kitamura, K. Takemoto, Jpn. Kokai Tokkyo Koho JP 04 91,093, 1992 [Chem. Abstr. 1992, 117, 171695u].
    • Noyori, R.1    Kitamura, M.2    Takemoto, K.3
  • 16
    • 85030277119 scopus 로고
    • b) R. Noyori, M. Kitamura, K. Takemoto, Jpn. Kokai Tokkyo Koho JP 04 91,093, 1992 [Chem. Abstr. 1992, 117, 171695u].
    • (1992) Chem. Abstr. , vol.117
  • 17
    • 0025390935 scopus 로고    scopus 로고
    • B. Wiedel, MOPAC61C, modified version of the original software by J. J. P. Stewart, J. Comput. Aided Mol. Des. 1990, 4, 1-105.
    • MOPAC61C
    • Wiedel, B.1
  • 19
    • 0642382526 scopus 로고    scopus 로고
    • Bardolino
    • 2-symmetric binaphthyl substituent synthesized by a different route, and its use in the enantioselective reduction of an α-bromoketone (10-41%ee), was recently presented: D. P. Curran, D. Nanni, Abstr. Pap. 7th Int. Symp. Org. Free Radicals, Bardolino, 1996, p. 66.
    • (1996) Abstr. Pap. 7th Int. Symp. Org. Free Radicals , pp. 66
    • Curran, D.P.1    Nanni, D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.