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Volumn 7, Issue 11, 1996, Pages 3247-3254

Chiral oxazolines linked to tetrathiafulvalene (TTF): Redox-active ligands for asymmetric synthesis

Author keywords

[No Author keywords available]

Indexed keywords

OXAZOLINE DERIVATIVE; TETRATHIAFULVALENE DERIVATIVE;

EID: 0030575843     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/0957-4166(96)00425-9     Document Type: Article
Times cited : (45)

References (42)
  • 3
    • 0011829479 scopus 로고
    • NATO ASI Series 6, Martins Nijhoft: Dordrecht, Chp.3
    • 2. For leading monographs see: (a) Bosnich, B. Asymmetric Synthesis, NATO ASI Series 6, 103, Martins Nijhoft: Dordrecht, 1986, Chp.3.
    • (1986) Asymmetric Synthesis , pp. 103
    • Bosnich, B.1
  • 29
    • 37049071580 scopus 로고
    • Special Issue on Molecular Conductors
    • (b) J. Mater. Chem., Special Issue on Molecular Conductors, 1995, 5, 1469-1760.
    • (1995) J. Mater. Chem. , vol.5 , pp. 1469-1760
  • 33
    • 0011831860 scopus 로고    scopus 로고
    • unpublished results
    • 15. Moore, A. J.; Bryce, M. R. unpublished results. (Cf. Panetta, C. A.; Baghdadchi, J.; Metzger, R. Mol. Cryst. Liq. Cryst., 1984, 707, 103).
    • Moore, A.J.1    Bryce, M.R.2
  • 37
    • 0000709515 scopus 로고
    • 18. Support for the assumption that no racemisation occurs during oxazoline formation is provided in Meyers, A. I.; Hoyer, D. Tetrahedron Lett., 1985, 26, 4687.
    • (1985) Tetrahedron Lett. , vol.26 , pp. 4687
    • Meyers, A.I.1    Hoyer, D.2
  • 42
    • 0011909091 scopus 로고    scopus 로고
    • note
    • 23. Allylpalladium chloride dimer could not be employed in these studies due to its decomposition under the conditions of the electrochemical measurements.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.