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Volumn 7, Issue 9, 1996, Pages 2501-2504

New chiral non-racemic piperidine-derived epoxy lactams

Author keywords

[No Author keywords available]

Indexed keywords

LACTAM DERIVATIVE; PIPERIDINE DERIVATIVE;

EID: 0030249234     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/0957-4166(96)00317-5     Document Type: Article
Times cited : (11)

References (35)
  • 10
    • 77957051048 scopus 로고
    • Brossi, A., Ed.; Academic Press, London
    • (b) Strunz, G. M.; Findlay, J. A. In The Alkaloids, Brossi, A., Ed.; Academic Press, London, 1985; Vol. 26, pp 89-183.
    • (1985) The Alkaloids , vol.26 , pp. 89-183
    • Strunz, G.M.1    Findlay, J.A.2
  • 11
    • 0011838270 scopus 로고
    • Cordell G. A., Ed; Academic Press, London
    • (c) Daly, J. W.; Garraffo, H. M.; Spande, T. F. In The Alkaloids, Cordell G. A., Ed; Academic Press, London, 1993; Vol. 43, pp 185-288.
    • (1993) The Alkaloids , vol.43 , pp. 185-288
    • Daly, J.W.1    Garraffo, H.M.2    Spande, T.F.3
  • 16
    • 0001046290 scopus 로고
    • 7. For other reports on the preparation of 1, see: (a) Royer, J.; Husson, H.-P. Heterocycles 1993, 36, 1493.
    • (1993) Heterocycles , vol.36 , pp. 1493
    • Royer, J.1    Husson, H.-P.2
  • 18
    • 0027934450 scopus 로고
    • 8. For a review on the synthesis of chiral epoxides, see: Besse, P.; Veschambre, H. Tetrahedron 1994, 50, 8885.
    • (1994) Tetrahedron , vol.50 , pp. 8885
    • Besse, P.1    Veschambre, H.2
  • 19
    • 85030271452 scopus 로고    scopus 로고
    • note
    • 5); 72.8 (C-2); 84.4 (C-8a); 161.3 (C=O); 164.6 (C=O).
  • 20
    • 85030279270 scopus 로고    scopus 로고
    • note
    • 3O); 55.9 (C-7); 56.3 (C-6); 59.2 (C-3); 72.7 (C-2); 84.3 (C-8a); 126.1 (C-o); 127.9 (C-p); 128.7 (C-m); 137.7 (C-ipso); 161.3 (C=O); 165.0 (C=O).
  • 21
    • 85030277526 scopus 로고    scopus 로고
    • note
    • 11. All yields are from material purified by column chromatography. Satisfactory analytical and/or spectral data were obtained for all new compounds.
  • 22
    • 0001045392 scopus 로고
    • 12. A similar mechanism has been proposed for the epoxidation of α,β-unsaturated ketones by hydroperoxide ion: House, H. O.; Ro, R. S. J. Am. Chem. Soc. 1958, 80, 2428.
    • (1958) J. Am. Chem. Soc. , vol.80 , pp. 2428
    • House, H.O.1    Ro, R.S.2
  • 23
    • 85030274931 scopus 로고    scopus 로고
    • note
    • -3. Complete data have been deposited at the Cambridge Crystallographic Data Centre.
  • 30
    • 0028900263 scopus 로고
    • To our knowledge there is only one example of the epoxidation of a conjugated six-membered lactam: see reference 16e
    • (e) Li, B.; Smith, M. B. Synthetic Commun. 1995, 25, 1265. To our knowledge there is only one example of the epoxidation of a conjugated six-membered lactam: see reference 16e.
    • (1995) Synthetic Commun. , vol.25 , pp. 1265
    • Li, B.1    Smith, M.B.2
  • 32
    • 85030279058 scopus 로고    scopus 로고
    • note
    • 3, 75 MHz) δ 29.5 (C-8); 56.6 (C-7); 59.3 (C-3); 72.9 (C-2); 84.6 (C-8a); 126.1 (C-o); 128.1 (C-p); 129.0 (C-m); 137.9 (C-ipso); 162.5 (C=O); 199.6 (C=O).
  • 33
    • 85030273828 scopus 로고    scopus 로고
    • note
    • 2O); 73.0 (C-2); 84.9 (C-8a); 126.0 (C-o); 128.0 (C-p); 128.9 (C-p); 137.9 (C-ipso); 166.3 (C=O).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.