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Volumn 43, Issue 1, 2000, Pages 40-50

The mechanism of asymmetric reduction catalyzed by a C2 symmetric bis-amino alcohol catalyst - In situ NMR study of the structure of new type of dual-centered catalyst

Author keywords

2D gradient experiment; Bis oxazaborolidine; Diaminodihydroxylborane; In situ NMR

Indexed keywords


EID: 0342266761     PISSN: 10069291     EISSN: None     Source Type: Journal    
DOI: 10.1007/bf03028848     Document Type: Article
Times cited : (8)

References (11)
  • 1
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    • (1987) Bull. Chem. Soc. Jpn. , vol.60 , pp. 395
    • Itsuno, S.1    Sakurai, Y.2    Ito, K.3
  • 2
    • 33845282886 scopus 로고
    • Highly enantioselective borane reduction of ketones catalyzed by chiral oxazaborolidines. Mechanism and synthetic implications
    • Corey, E. J., Bakshi, R. K., Shibata, S., Highly enantioselective borane reduction of ketones catalyzed by chiral oxazaborolidines. Mechanism and synthetic implications, J. Am. Chem. Soc., 1987, 109: 5551.
    • (1987) J. Am. Chem. Soc. , vol.109 , pp. 5551
    • Corey, E.J.1    Bakshi, R.K.2    Shibata, S.3
  • 4
    • 0030442525 scopus 로고    scopus 로고
    • The structure of chiral oxazaborolidine and the enantioselective borane reduction of propiophenone
    • Jiang, Y-Z, Qin, Y., Mi. A-Q. et al., The structure of chiral oxazaborolidine and the enantioselective borane reduction of propiophenone, Chinese J. of Organic Chemistry, 1996, 16:29.
    • (1996) Chinese J. of Organic Chemistry , vol.16 , pp. 29
    • Jiang, Y.-Z.1    Qin, Y.2    Mi, A.-Q.3
  • 5
    • 33845185615 scopus 로고
    • Practical enantioselective Diels-Alder and Aldol reactiions using a new chiral controller system
    • Corey, E J., Imwinkelried, R., Pikui, S. et al., Practical enantioselective Diels-Alder and Aldol reactiions using a new chiral controller system, J. Am. Chem. Soc., 1989, 111: 5493.
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 5493
    • Corey, E.J.1    Imwinkelried, R.2    Pikui, S.3
  • 6
    • 0030472830 scopus 로고    scopus 로고
    • Asymmetric two-center catalysis-learning from nature
    • Steinhagen, H., Helmehen, G., Asymmetric two-center catalysis-learning from nature, Angew. Chem., Int. Ed. Engl., 1996, 35(30): 2339.
    • (1996) Angew. Chem., Int. Ed. Engl. , vol.35 , Issue.30 , pp. 2339
    • Steinhagen, H.1    Helmehen, G.2
  • 7
    • 85047672054 scopus 로고
    • A practical synthesis of nonpeptide cyclic ureas as potent HIV protease inhibitors
    • Rassano, L. T., Lo, Y. S., Anzalone, L., et al., A practical synthesis of nonpeptide cyclic ureas as potent HIV protease inhibitors, Tetrahedron Letter, 1995, 36: 4967.
    • (1995) Tetrahedron Letter , vol.36 , pp. 4967
    • Rassano, L.T.1    Lo, Y.S.2    Anzalone, L.3
  • 8
    • 0039390765 scopus 로고    scopus 로고
    • Preparation of chiral bis-β-amino alcohols and their application in the enantioselective catalytic borane reduction of aromatic ketones
    • Li, X-Z, Xie, R-G., Preparation of chiral bis-β-amino alcohols and their application in the enantioselective catalytic borane reduction of aromatic ketones, Chinese J. Organic Chemistry, 1998, 18: 142.
    • (1998) Chinese J. Organic Chemistry , vol.18 , pp. 142
    • Li, X.-Z.1    Xie, R.-G.2
  • 11
    • 84943982238 scopus 로고
    • 11B-NMR-Spektroskopic zur Untersuchung von hydroborierungen, 1 hydroborierungen von 3-methyl-1.3-butadien mit boran in tetrahydrofuran und dimethylsulfid
    • 11B-NMR-Spektroskopic zur Untersuchung von hydroborierungen, 1 hydroborierungen von 3-methyl-1.3-butadien mit boran in tetrahydrofuran und dimethylsulfid. Naturtorsch B: Anorg. Chem., Org. Chem., 1980, 35B(10): 1229.
    • (1980) Naturtorsch B: Anorg. Chem., Org. Chem. , vol.35 B , Issue.10 , pp. 1229
    • Contreras, R.1    Wrackmeyer, B.Z.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.