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Volumn 54, Issue 37, 1998, Pages 11247-11254

Monobenzylether of (R,R)-1,2-diphenylethane-1,2-diol as chiral auxiliary in the diastereoselective reduction of α-ketoesters

Author keywords

[No Author keywords available]

Indexed keywords

BENZENE DERIVATIVE; ESTER; ETHANE; ETHER DERIVATIVE;

EID: 0032505218     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(98)00657-7     Document Type: Article
Times cited : (31)

References (34)
  • 4
    • 0003978131 scopus 로고
    • American Chemical Society: Washington D.C., USA, Chapter 2
    • 2. For a review see: Morrison, J. D.; Mosher, H. S. Asymmetric Organic Reactions; American Chemical Society: Washington D.C., USA, 1976; Chapter 2, p 50.
    • (1976) Asymmetric Organic Reactions , pp. 50
    • Morrison, J.D.1    Mosher, H.S.2
  • 21
    • 0000778942 scopus 로고    scopus 로고
    • The importance of π-π interaction in asymmetric synthesis has been recently pointed out
    • (d) Dumas, F.; Mesrhab, B.; d'Angelo, J.; Riche, C.; Chiaroni, A. J. Org. Chem. 1996, 61, 2293. The importance of π-π interaction in asymmetric synthesis has been recently pointed out: Jones, G. B.; Chapman, B. J. Synthesis 1995, 475. For a recent discussion about the arene-arene interactions see: Hunter, C. A. Angew. Chem. Int. Ed. Engl. 1993, 32, 1585. Hunter, C. A. Chem. Soc. Rev. 1994, 101. Cozzi, F.; Siegel, J. S. Pure Appl. Chem. 1995, 67, 1995.
    • (1996) J. Org. Chem. , vol.61 , pp. 2293
    • Dumas, F.1    Mesrhab, B.2    D'Angelo, J.3    Riche, C.4    Chiaroni, A.5
  • 22
    • 0029066475 scopus 로고
    • (d) Dumas, F.; Mesrhab, B.; d'Angelo, J.; Riche, C.; Chiaroni, A. J. Org. Chem. 1996, 61, 2293. The importance of π-π interaction in asymmetric synthesis has been recently pointed out: Jones, G. B.; Chapman, B. J. Synthesis 1995, 475. For a recent discussion about the arene-arene interactions see: Hunter, C. A. Angew. Chem. Int. Ed. Engl. 1993, 32, 1585. Hunter, C. A. Chem. Soc. Rev. 1994, 101. Cozzi, F.; Siegel, J. S. Pure Appl. Chem. 1995, 67, 1995.
    • (1995) Synthesis , pp. 475
    • Jones, G.B.1    Chapman, B.J.2
  • 23
    • 0000056388 scopus 로고
    • (d) Dumas, F.; Mesrhab, B.; d'Angelo, J.; Riche, C.; Chiaroni, A. J. Org. Chem. 1996, 61, 2293. The importance of π-π interaction in asymmetric synthesis has been recently pointed out: Jones, G. B.; Chapman, B. J. Synthesis 1995, 475. For a recent discussion about the arene-arene interactions see: Hunter, C. A. Angew. Chem. Int. Ed. Engl. 1993, 32, 1585. Hunter, C. A. Chem. Soc. Rev. 1994, 101. Cozzi, F.; Siegel, J. S. Pure Appl. Chem. 1995, 67, 1995.
    • (1993) Angew. Chem. Int. Ed. Engl. , vol.32 , pp. 1585
    • Hunter, C.A.1
  • 24
    • 0001894947 scopus 로고
    • (d) Dumas, F.; Mesrhab, B.; d'Angelo, J.; Riche, C.; Chiaroni, A. J. Org. Chem. 1996, 61, 2293. The importance of π-π interaction in asymmetric synthesis has been recently pointed out: Jones, G. B.; Chapman, B. J. Synthesis 1995, 475. For a recent discussion about the arene-arene interactions see: Hunter, C. A. Angew. Chem. Int. Ed. Engl. 1993, 32, 1585. Hunter, C. A. Chem. Soc. Rev. 1994, 101. Cozzi, F.; Siegel, J. S. Pure Appl. Chem. 1995, 67, 1995.
    • (1994) Chem. Soc. Rev. , pp. 101
    • Hunter, C.A.1
  • 25
    • 0001579080 scopus 로고
    • (d) Dumas, F.; Mesrhab, B.; d'Angelo, J.; Riche, C.; Chiaroni, A. J. Org. Chem. 1996, 61, 2293. The importance of π-π interaction in asymmetric synthesis has been recently pointed out: Jones, G. B.; Chapman, B. J. Synthesis 1995, 475. For a recent discussion about the arene-arene interactions see: Hunter, C. A. Angew. Chem. Int. Ed. Engl. 1993, 32, 1585. Hunter, C. A. Chem. Soc. Rev. 1994, 101. Cozzi, F.; Siegel, J. S. Pure Appl. Chem. 1995, 67, 1995.
    • (1995) Pure Appl. Chem. , vol.67 , pp. 1995
    • Cozzi, F.1    Siegel, J.S.2
  • 31
    • 85038535642 scopus 로고    scopus 로고
    • 1H NMR and literature data, as discussed above. Work is now in progress in order to establish the minimum energy conformation both by a more detailed analysis of the NMR spectra and by molecular mechanics calculations
    • 1H NMR and literature data, as discussed above. Work is now in progress in order to establish the minimum energy conformation both by a more detailed analysis of the NMR spectra and by molecular mechanics calculations.
  • 32
    • 0003816070 scopus 로고    scopus 로고
    • HC*-C*H value can be obtained by the classical Karplus equation, assuming an equal molar ratio for the three conformers. see for instance: EdiSES: Napoli
    • HC*-C*H value can be obtained by the classical Karplus equation, assuming an equal molar ratio for the three conformers. (see for instance: Hesse, M.; Meier, H.; Zeeh, B. Metodi Spettroscopici nella Chimica Organica; EdiSES: Napoli, 1996)
    • (1996) Metodi Spettroscopici Nella Chimica Organica
    • Hesse, M.1    Meier, H.2    Zeeh, B.3
  • 33
    • 85038537257 scopus 로고    scopus 로고
    • See ref. 2 p 84
    • 14. See ref. 2 p 84.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.