메뉴 건너뛰기




Volumn 54, Issue 26, 1998, Pages 7229-7271

Anomeric amides - Structure, properties and reactivity

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE;

EID: 0032565904     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(98)00197-5     Document Type: Review
Times cited : (92)

References (141)
  • 20
    • 0003244794 scopus 로고
    • Stereoelectronic Effects in Organic Chemistry
    • Baldwin, J. E. F. Ed.; Pergamon Press: Oxford
    • 20. Deslongchamps, P. Stereoelectronic Effects in Organic Chemistry, Organic Chemistry Series Vol. 1; Baldwin, J. E. F. Ed.; Pergamon Press: Oxford, 1984; p. 4.
    • (1984) Organic Chemistry Series , vol.1 , pp. 4
    • Deslongchamps, P.1
  • 22
    • 0010476736 scopus 로고    scopus 로고
    • Oxford Chemistry Primers; Davies, S. G. Ed.; Oxford University Press: Oxford
    • 22. Kirby, A. J. Stereoetectronic Effects, Oxford Chemistry Primers; Davies, S. G. Ed.; Oxford University Press: Oxford, 1996.
    • (1996) Stereoetectronic Effects
    • Kirby, A.J.1
  • 24
    • 0010439370 scopus 로고    scopus 로고
    • For an excellent overview of anomeric effects on conformation in six-membered ring systems see Reference 22; see also Reference 21, Ch. 11, Section 4g
    • 24. For an excellent overview of anomeric effects on conformation in six-membered ring systems see Reference 22; see also Reference 21, Ch. 11, Section 4g.
  • 27
    • 0010511766 scopus 로고    scopus 로고
    • See Reference 23, Ch. 4, p. 94
    • 27. See Reference 23, Ch. 4, p. 94.
  • 29
    • 0010437639 scopus 로고    scopus 로고
    • See Reference 21, p. 612
    • 29. See Reference 21, p. 612.
  • 30
    • 0001918171 scopus 로고
    • Structural Theory of Organic Chemistry
    • Springer-Verlag: Berlin, Part IV, pp. 177-183
    • 30. Epiotis, N. D.; Cherry, W. R.; Shaik, S.; Yates, Y. L.; Bernardi, F. Structural Theory of Organic Chemistry, Topics in Current Chemistry; Springer-Verlag: Berlin, 1977; Part I, pp. 3-27, Part IV, pp. 177-183.
    • (1977) Topics in Current Chemistry , Issue.PART I , pp. 3-27
    • Epiotis, N.D.1    Cherry, W.R.2    Shaik, S.3    Yates, Y.L.4    Bernardi, F.5
  • 34
    • 0004105856 scopus 로고
    • Longman Scientific and Technical: New York
    • 34. Isaacs, N. S. Physical Organic Chemistry; Longman Scientific and Technical: New York, 1995; p. 176.
    • (1995) Physical Organic Chemistry , pp. 176
    • Isaacs, N.S.1
  • 38
    • 0010478595 scopus 로고    scopus 로고
    • See Reference 30, pp. 49-54
    • 38. See Reference 30, pp. 49-54
  • 40
    • 0010476737 scopus 로고    scopus 로고
    • -1; see Reference 41
    • -1; see Reference 41.
  • 52
    • 0010435819 scopus 로고    scopus 로고
    • See Reference 28, p. 142
    • 52. See Reference 28, p. 142.
  • 83
    • 0010477445 scopus 로고
    • The Decompositions of Peroxides and Azoalkanes
    • Kochi, J. K. Ed.; John Wiley and Sons: New York
    • -1; see Koenig, T. The Decompositions of Peroxides and Azoalkanes. In Free Radicals; Kochi, J. K. Ed.; John Wiley and Sons: New York, 1973; Vol. 1; p. 113.
    • (1973) Free Radicals , vol.1 , pp. 113
    • Koenig, T.1
  • 99
    • 0010435439 scopus 로고    scopus 로고
    • Unpublished results
    • 99. Glover, S. A. Unpublished results.
    • Glover, S.A.1
  • 101
    • 0010511172 scopus 로고    scopus 로고
    • See Reference 34 p 511
    • 101. See Reference 34 p 511.
  • 102
    • 0010438803 scopus 로고    scopus 로고
    • See Reference 34 p.515 and cited references
    • 102. See Reference 34 p.515 and cited references.
  • 105
    • 0010478598 scopus 로고    scopus 로고
    • Unpublished results
    • 105. Several N-acyloxy-N-alkoxybenzamides have been shown to react at the 5′ N-7 of GG sequences; Banks, T; Glover, S.A.; Prakash, A.S.; Rowbottom, C.A. Unpublished results.
    • Banks, T.1    Glover, S.A.2    Prakash, A.S.3    Rowbottom, C.A.4
  • 106
    • 0010436145 scopus 로고    scopus 로고
    • Unpublished results
    • 106. At 1μmol/plate, N-acetoxy-N-butoxy-2-naphthamide and N-acetoxy-N-butoxybenzamide gave 5508 and 477 revenants respectively in Salmonella TA100 without metabolic activation; Bonin, A.M.; Glover, S.A.; Rowbottom, C.A. Unpublished results.
    • Bonin, A.M.1    Glover, S.A.2    Rowbottom, C.A.3
  • 112
  • 114
    • 0003158891 scopus 로고
    • Conformational Analysis of Hydrazines
    • Patai, S. Ed.; John Wiley and Sons: London
    • 114. Shvo, Y. Conformational Analysis of Hydrazines. In The chemistry of the hydrazo, azo and azoxy groups Part 2; Patai, S. Ed.; John Wiley and Sons: London, 1975; pp. 1017-1095.
    • (1975) The Chemistry of the Hydrazo, Azo and Azoxy Groups Part 2 , pp. 1017-1095
    • Shvo, Y.1
  • 119
    • 0010439754 scopus 로고    scopus 로고
    • See Reference 114, p. 1035
    • 119. See Reference 114, p. 1035.
  • 121
    • 0010436147 scopus 로고    scopus 로고
    • See Reference 114, pp. 1076, 1080
    • 121. See Reference 114, pp. 1076, 1080
  • 130
    • 0010480486 scopus 로고    scopus 로고
    • Cooley (Reference 5) reported a α correlation with ρ = -0.47 for the same series in chloroform; rate constants were not given
    • 130. Cooley (Reference 5) reported a α correlation with ρ = -0.47 for the same series in chloroform; rate constants were not given.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.