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Volumn 9, Issue 3, 1998, Pages 407-422

Enantioselective catalysis. Part 119: New chiral 2-(2- pyridinyl)oxazoline ligands containing an additional optically active substituent in the pyridine system

Author keywords

[No Author keywords available]

Indexed keywords

2 (2 PYRIDINYL)OXAZOLINE; OXAZOLINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0032512603     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(97)00619-8     Document Type: Article
Times cited : (36)

References (36)
  • 3
    • 2842564022 scopus 로고
    • Transition metal catalyzed reactions
    • Eds.: G. Helmchen, R. W. Hoffmann, J. Mulzer, E. Schaumann, Thieme, Stuttgart, New York and references therein
    • 3. H. Brunner, Transition Metal Catalyzed Reactions in Houben-Weyl, Vol. E 21d, Stereoselective Synthesis (Eds.: G. Helmchen, R. W. Hoffmann, J. Mulzer, E. Schaumann), Thieme, Stuttgart, New York 1995, 4074-4081 and references therein.
    • (1995) Houben-Weyl, Vol. E 21d, Stereoselective Synthesis , pp. 4074-4081
    • Brunner, H.1
  • 16
    • 0010339791 scopus 로고    scopus 로고
    • Since (+)-pinocarvone was prepared from (-)-α-pinene (ca. 80% ee) 10% of the other enantiomer was present. Hence, after synthesis of the chiral oxazoline 9 there might be a mixture of diastereomers
    • 16. Since (+)-pinocarvone was prepared from (-)-α-pinene (ca. 80% ee) 10% of the other enantiomer was present. Hence, after synthesis of the chiral oxazoline 9 there might be a mixture of diastereomers.
  • 17
    • 0010388058 scopus 로고    scopus 로고
    • In this paper L-menthyl-represents [(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl]-and D-menthyl-represents [(1S,2R,5S)-2-isopropyl-5-methylcyclohexyl]-
    • 17. In this paper L-menthyl-represents [(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl]-and D-menthyl-represents [(1S,2R,5S)-2-isopropyl-5-methylcyclohexyl]-.
  • 20
    • 0010418367 scopus 로고
    • Ph.D. Thesis, Stanford University
    • 20. S. G. Hentges, Ph.D. Thesis, Stanford University 1980.
    • (1980)
    • Hentges, S.G.1
  • 25
    • 33845550434 scopus 로고
    • 25. General procedure: W. K. Fife, J. Org. Chem. 1983, 48, 1375-1377.
    • (1983) J. Org. Chem. , vol.48 , pp. 1375-1377
    • Fife, W.K.1
  • 30
    • 0010383174 scopus 로고    scopus 로고
    • We thank Prof. A. von Zelewsky, University of Fribourg (Switzerland) for providing this compound
    • 30. We thank Prof. A. von Zelewsky, University of Fribourg (Switzerland) for providing this compound.
  • 33
    • 0010341897 scopus 로고    scopus 로고
    • 4 to improve the performance of Rh-catalysed asymmetric hydrosilylations has been reported (e.g. Refs. 6 and 7)
    • 4 to improve the performance of Rh-catalysed asymmetric hydrosilylations has been reported (e.g. Refs. 6 and 7).
  • 35
    • 0029965916 scopus 로고    scopus 로고
    • 35. The CIP-nomenclature of related compounds (e.g. Ref. 12 and G. Chelucci, M. A. Cabras, Tetrahedron: Asymmetry 1996, 7, 965-966) is in error. The correct configuration of 3-9 at C-5 is R (C-4a/C-8a has priority with respect to C-9/C-7) and at C-7 also R (priority sequence: C-9>C-8/C-8a>C-6/C-5).
    • (1996) Tetrahedron: Asymmetry , vol.7 , pp. 965-966
    • Chelucci, G.1    Cabras, M.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.