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Volumn 58, Issue 21, 1993, Pages 5620-5623

Electrophilic Amination of Higher Order Cuprates with N,O-Bis (trimethylsilyl)hydroxylamine

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EID: 10144230587     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo00073a018     Document Type: Article
Times cited : (73)

References (30)
  • 8
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    • and references cited therein
    • Beak, P.; Selling, G. W. J. Org. Chem. 1989, 54, 5574 and references cited therein.
    • (1989) J. Org. Chem. , vol.54 , pp. 5574
    • Beak, P.1    Selling, G.W.2
  • 13
    • 0001899449 scopus 로고
    • and references cited therein
    • Nakamura, E. Synlett 1991, 539 and references cited therein.
    • (1991) Synlett , pp. 539
    • Nakamura, E.1
  • 19
    • 0001878909 scopus 로고
    • and references cited therein
    • Lipshutz, B. H. Synlett 1990, 119 and references cited therein.
    • (1990) Synlett , pp. 119
    • Lipshutz, B.H.1
  • 22
    • 0007101263 scopus 로고
    • The proposal for dimeric structures in LO cuprates has been confirmed by molecular weight determinations and NMR spectroscopy and amply demonstrated by X-ray crystallography:, and references cited therein
    • The proposal for dimeric structures in LO cuprates has been confirmed by molecular weight determinations and NMR spectroscopy and amply demonstrated by X-ray crystallography: Snyder, J. P.; Tipsword, G. E.; Spangler, D. P. J. Am. Chem. Soc. 1992, 114, 1507 and references cited therein.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 1507
    • Snyder, J.P.1    Tipsword, G.E.2    Spangler, D.P.3
  • 23
    • 37049118084 scopus 로고
    • Although literature data suggest a higher stability with aromatic groups, a structure in LO cuprates in which the alkyl bridge again involves a three-center two-electron bond, with linear coordination at copper, has also been demonstrated
    • Although literature data suggest a higher stability with aromatic groups, a structure in LO cuprates in which the alkyl bridge again involves a three-center two-electron bond, with linear coordination at copper, has also been demonstrated: Jarvis, J. A. J.; Kilbourn, B. T.; Pearce, R.; Lappert, M. F. J. Chem. Soc., Chem. Commun. 1973, 475.
    • (1973) J. Chem. Soc., Chem. Commun. , pp. 475
    • Jarvis, J.A.J.1    Kilbourn, B.T.2    Pearce, R.3    Lappert, M.F.4
  • 28
    • 0003522704 scopus 로고
    • The oxidation potential data for Ph (<−0.1 V) and Me (−0.5 V), Springer: Berlin) suggest a decrease in hardness in moving from the aromatic to the aliphatic series and therefore support a more favorable interaction of aromatic and heteroaromatic ligands as compared with that of the alkyl groups with the harder N heteroatom
    • The oxidation potential data for Ph (<−0.1 V) and Me (−0.5 V) (Eberson, L. In Electron transfer reactions in Organic Chemistry; Springer: Berlin, 1987) suggest a decrease in hardness in moving from the aromatic to the aliphatic series and therefore support a more favorable interaction of aromatic and heteroaromatic ligands as compared with that of the alkyl groups with the harder N heteroatom.
    • (1987) Electron transfer reactions in Organic Chemistry
    • Eberson, L.1


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