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0001046290
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7. For other reports on the preparation of 1, see: (a) Royer, J.; Husson, H.-P. Heterocycles 1993, 36, 1493.
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8. For a review on the synthesis of chiral epoxides, see: Besse, P.; Veschambre, H. Tetrahedron 1994, 50, 8885.
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Besse, P.1
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19
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85030271452
-
-
note
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5); 72.8 (C-2); 84.4 (C-8a); 161.3 (C=O); 164.6 (C=O).
-
-
-
-
20
-
-
85030279270
-
-
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
-
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85030277526
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-
note
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11. All yields are from material purified by column chromatography. Satisfactory analytical and/or spectral data were obtained for all new compounds.
-
-
-
-
22
-
-
0001045392
-
-
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.
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J. Am. Chem. Soc.
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House, H.O.1
Ro, R.S.2
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23
-
-
85030274931
-
-
note
-
-3. Complete data have been deposited at the Cambridge Crystallographic Data Centre.
-
-
-
-
26
-
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0025040045
-
-
16. (a) Romo, D.; Romine, J. L.; Midura, W.; Meyers, A. I. Tetrahedron 1990, 46, 4951.
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Romo, D.1
Romine, J.L.2
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Meyers, A.I.4
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28
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0027953364
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(c) Herdeis, C.; Hubmann, H. P.; Lotter, H. Tetrahedron: Asymmetry 1994, 5, 119.
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Lotter, H.3
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0028966223
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(d) Andres, C. J.; Spetseris, N.; Norton, J. R.; Meyers, A. I. Tetrahedron Lett. 1995, 36, 1613.
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Andres, C.J.1
Spetseris, N.2
Norton, J.R.3
Meyers, A.I.4
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30
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0028900263
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-
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.
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Synthetic Commun.
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-
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Li, B.1
Smith, M.B.2
-
32
-
-
85030279058
-
-
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
-
-
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).
-
-
-
-
34
-
-
0020112101
-
-
20. For reviews, see: (a) Sharpless, K. B.; Behrens, C. H.; Katsuki, T.; Lee, A. W. M.; Martin, V. S.; Takatani, M.; Viti, S. M.; Walker, F. J.; Woodard, S. S. Pure Appl. Chem. 1983, 55, 589.
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Pure Appl. Chem.
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, pp. 589
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Sharpless, K.B.1
Behrens, C.H.2
Katsuki, T.3
Lee, A.W.M.4
Martin, V.S.5
Takatani, M.6
Viti, S.M.7
Walker, F.J.8
Woodard, S.S.9
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