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15
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0001117371
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Davis F.A., Zhou P., Murphy C.K., Sundarababu G., Qi H., Han W., Przeslawski R.M., Chen B.-J., and Carroll P.J. J. Org. Chem. 63 (1998) 2273-2280
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Davis, F.A.1
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Przeslawski, R.M.7
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17
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0035804499
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Cahard D., Audouard C., Plaquevent J.-C., Toupet L., and Roques N. Tetrahedron Lett. 42 (2001) 1867
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Cahard, D.1
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29
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0000836901
-
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For a review on structure, reactivity and chemistry of fluoroalkyl radicals, see:
-
For a review on structure, reactivity and chemistry of fluoroalkyl radicals, see:. Dolbier Jr. W.R. Chem. Rev. 96 (1996) 1557-1584
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Dolbier Jr., W.R.1
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30
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0027219236
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For a review on manganese(III)-mediated reactions, see:
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For a review on manganese(III)-mediated reactions, see:. Melikyan G.G. Synthesis (1993) 833-850
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Melikyan, G.G.1
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31
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0026535899
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For a review on the selective oxidation of α,β-unsaturated ketones in α′-position, see:
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For a review on the selective oxidation of α,β-unsaturated ketones in α′-position, see:. Demir A., and Jeganathan A. Synthesis (1992) 235-247
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Demir, A.1
Jeganathan, A.2
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32
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0000507386
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For applications of ceric ammonium nitrate, see:
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For applications of ceric ammonium nitrate, see:. Rueck K., and Kunz H. J. Prakt. Chem. 336 (1994) 470-472
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Rueck, K.1
Kunz, H.2
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33
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33846307752
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For a review on cerium(IV)-mediated reactions, see:
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For a review on cerium(IV)-mediated reactions, see:. Nair V., Mathew J., and Prabhakaran J. Chem. Soc. Rev. (1997) 127-132
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Nair, V.1
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34
-
-
34247554227
-
-
note
-
2O (1.35 g, 5.0 mmol), potassium acetate (1.0 g) and olefin (1.0 mL) and heated in a pressure tube for 20 min (temperature of surrounding oil bath: 140 °C). The reaction mixture was cooled, diluted with water, and extracted twice with dichloromethane. The combined organic extracts were dried over sodium sulfate, concentrated and purified by flash column chromatography to give tetralones 2 as colorless oils.
-
-
-
-
35
-
-
34247552741
-
-
note
-
3): δ 3.6
-
-
-
-
36
-
-
34247603030
-
-
note
-
An experiment with α-fluoroacetophenone (1a) and 1-octene run under the conditions described in the general procedure Ref. 18 showed complete disappearance of 1a after 8 min.
-
-
-
-
37
-
-
0001754635
-
-
For vicinal proton-fluorine spin-spin couplings, see:
-
For vicinal proton-fluorine spin-spin couplings, see:. Williamson K.L., Hsu Y.-F.L., Hall F.H., Swager S., and Coulter M.S. J. Am. Chem. Soc. 90 (1968) 6717-6722
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Williamson, K.L.1
Hsu, Y.-F.L.2
Hall, F.H.3
Swager, S.4
Coulter, M.S.5
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38
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-
0000728171
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-
For vicinal endo-endo and exo-exo spin-spin couplings in norbornanes, see:
-
For vicinal endo-endo and exo-exo spin-spin couplings in norbornanes, see:. Marshall J.L., Walter S.R., Barfield M., Marchand A.P., Marchand N.W., and Segre A.L. Tetrahedron 32 (1976) 537-542
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Marshall, J.L.1
Walter, S.R.2
Barfield, M.3
Marchand, A.P.4
Marchand, N.W.5
Segre, A.L.6
-
39
-
-
34247591398
-
-
note
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3 (0.0 ppm).
-
-
-
-
40
-
-
0002727973
-
-
For lactone formation, both a radical attack on the carbonyl oxygen atom and on the manganese have been proposed:
-
For lactone formation, both a radical attack on the carbonyl oxygen atom and on the manganese have been proposed:. Fristad W.E., and Peterson J.R. J. Org. Chem. 50 (1985) 10-18
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Fristad, W.E.1
Peterson, J.R.2
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41
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0000057422
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-
Renaud P., and Sibi M.P. (Eds), Wiley-VCH, Weinheim
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Snider B.B. In: Renaud P., and Sibi M.P. (Eds). Radicals in Organic Synthesis. 1st ed. Vol. 1 (2001), Wiley-VCH, Weinheim 198-218
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-
Snider, B.B.1
-
42
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-
34247578617
-
-
+) 236.0849. Found: 236.0849.
-
-
-
-
43
-
-
34247571394
-
-
+) 216.1514. Found: 216.1517.
-
-
-
-
44
-
-
0000382065
-
-
Santi R., Bergamini F., Citterio A., Sebastiano R., and Nicolini M. J. Org. Chem. 57 (1992) 4250-4255
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Santi, R.1
Bergamini, F.2
Citterio, A.3
Sebastiano, R.4
Nicolini, M.5
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45
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-
0001104642
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-
For a characterization of (Z)-3-phenyl-2-pentenal, see:
-
For a characterization of (Z)-3-phenyl-2-pentenal, see:. Chou S.-S.P., Kuo H.-L., Wang C.-J., Tsai C.-Y., and Sun C.-M. J. Org. Chem. 54 (1989) 868-872
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Chou, S.-S.P.1
Kuo, H.-L.2
Wang, C.-J.3
Tsai, C.-Y.4
Sun, C.-M.5
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46
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0002743531
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-
For cyclizations of vinyl radicals on aryl rings, see:
-
For cyclizations of vinyl radicals on aryl rings, see:. Montevecchi P.C., and Navacchia M.L. J. Org. Chem. 63 (1998) 537-542
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Montevecchi, P.C.1
Navacchia, M.L.2
-
47
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34247609895
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-
note
-
For the formation of aldehyde 4, the following mechanism is proposed: {A figure is presented}
-
-
-
-
48
-
-
24044451193
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For the radical Smiles-type rearrangement, see:
-
For the radical Smiles-type rearrangement, see:. Bacque E., El Qacemi M., and Zard S.Z. Org. Lett. 7 (2005) 3817-3820
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Bacque, E.1
El Qacemi, M.2
Zard, S.Z.3
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