-
6
-
-
85033148903
-
-
note
-
11 should be in agreement with a more extensive bond formation at the site adjacent to the heteroatom.
-
-
-
-
10
-
-
0001382427
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-
(a) Fringuelli, F.; Germani, R.; Pizzo, F.; Savelli, G. Tetrahedron Lett. 1989, 30, 1427.
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Fringuelli, F.1
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11
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0009672226
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(b) Fringuelli, F.; Pizzo, F.; Germani, R.; Savelli, G. Org. Prep. Proced. Int. 1989, 21, 757.
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Fringuelli, F.1
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12
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0001580329
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(a) Fringuelli, F.; Germani, R.; Pizzo, F.; Santinelli, F.; Savelli, G. J. Org. Chem. 1992, 57, 1198.
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Fringuelli, F.1
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13
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33947294185
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(b) Curci, R.; Di Prete, R. A.; Edwars, J. O.; Modena, G. J. Org. Chem. 1970, 35, 740.
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Curci, R.1
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18
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0030026262
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(d) Kluge, R.; Shulz, M.; Liebisch, S. Tetrahedron 1996, 52, 2957.
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Kluge, R.1
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22
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0001627220
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(h) Mori, K.; Hazra, B. G.; Pfeiffer, R. J.; Gupta, A. K.; Lindgren, B. S. Tetrahedron 1987, 43, 2249.
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Mori, K.1
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Lindgren, B.S.5
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24
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0342881496
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(j) Itoh, T.; Jitsukawa, K.; Kaneda, K.; Teranishi, S. J. Am. Chem. Soc. 1979, 101, 159.
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Itoh, T.1
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Teranishi, S.4
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26
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-
85033137626
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-
7b
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7b
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-
-
-
31
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-
85033136671
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-
6a
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6a
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-
-
-
32
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0037517511
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(a) Fringuelli, F.; Germani. R.; Pizzo, F.; Savelli, G. Gazz. Chim. Ital. 1989, 119, 249.
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Fringuelli, F.1
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33
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0027858331
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(b) Fringuelli, F.; Pellegrino, R.; Pizzo, F. Synth. Commun. 1993, 23, 3157.
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Fringuelli, F.1
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34
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0028060422
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(c) Fringuelli, F.; Pellegrino, R.; Piermatti, O.; Pizzo, F. Synth. Commun. 1994, 24, 2665.
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Fringuelli, F.1
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35
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0027930603
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(d) Fringuelli, F.; Pani, G.; Piermatti, O.; Pizzo, F. Tetrahedron 1994, 50, 11499.
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36
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0000941772
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(e) Brufola, G.; Fringuelli, F.; Piermatti, O.; Pizzo, F. Heterocycles 1996, 43, 1257.
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Brufola, G.1
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37
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-
85033132473
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-
10 The reaction time is not always optimized
-
10 The reaction time is not always optimized.
-
-
-
-
38
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-
85033153490
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-
7j
-
7j
-
-
-
39
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-
37049080091
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-
Jones, P.; Hagget, M. L.; Holden, D.; Robinson, P. J.; Edwards, J. O.; Bakofer, S. J.; Hayden, Y. T. J. Chem. Soc., Perkin Trans. 2 1989, 443.
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Jones, P.1
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Robinson, P.J.4
Edwards, J.O.5
Bakofer, S.J.6
Hayden, Y.T.7
-
40
-
-
85033140036
-
-
6a In strong alkaline medium the transition state of the epoxidation is a bis-anion or a mono-anion depending on the peroxy acid used
-
6a In strong alkaline medium the transition state of the epoxidation is a bis-anion or a mono-anion depending on the peroxy acid used.
-
-
-
-
41
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-
85033141657
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-
7a
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7a
-
-
-
42
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-
4243597363
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-
Wiley: New York; Coll.
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Böhme H. Organic Synthesis; Wiley: New York, 1955; Coll. Vol. 3, p 619.
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Böhme, H.1
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