-
1
-
-
33751142878
-
-
(a) Minisci, F.; Fontana, F.; Vismara, E. Gazz. Chim. Ital. 1993, 123, 9-18.
-
(1993)
Gazz. Chim. Ital
, vol.123
, pp. 9-18
-
-
Minisci, F.1
Fontana, F.2
Vismara, E.3
-
5
-
-
14844354033
-
-
(b) Cannella, R.; Clerici, A.; Pastori, N.; Regolini, E.; Porta, O. Org. Lett. 2005, 7, 645-648.
-
(2005)
Org. Lett
, vol.7
, pp. 645-648
-
-
Cannella, R.1
Clerici, A.2
Pastori, N.3
Regolini, E.4
Porta, O.5
-
7
-
-
27644539170
-
-
(a) Clerici, A.; Cannella, R.; Panzeri, W.; Pastori, N.; Regolini, E.; Porta, O. Tetrahedron Lett. 2005, 46, 8351-8354.
-
(2005)
Tetrahedron Lett
, vol.46
, pp. 8351-8354
-
-
Clerici, A.1
Cannella, R.2
Panzeri, W.3
Pastori, N.4
Regolini, E.5
Porta, O.6
-
8
-
-
33747342194
-
-
(b) Clerici, A.; Cannella, R.; Pastori, N.; Panzeri, W.; Porta, O. Tetrahedron 2006, 62, 5986-5994.
-
(2006)
Tetrahedron
, vol.62
, pp. 5986-5994
-
-
Clerici, A.1
Cannella, R.2
Pastori, N.3
Panzeri, W.4
Porta, O.5
-
10
-
-
2942545129
-
-
Galii, C. Chem. Rev. 1988, 88, 765-792.
-
(1988)
Chem. Rev
, vol.88
, pp. 765-792
-
-
Galii, C.1
-
11
-
-
37049094859
-
-
For intramolecular additions of aryl radicals to nonactivated olefins, see: a
-
For intramolecular additions of aryl radicals to nonactivated olefins, see: (a) Beckwith, A. L. J.; Meijs, G. F. J. Chem. Soc., Chem. Commun. 1981, 595-597.
-
(1981)
J. Chem. Soc., Chem. Commun
, pp. 595-597
-
-
Beckwith, A.L.J.1
Meijs, G.F.2
-
12
-
-
1642348801
-
-
(b) Vaillard, S. E.; Postigo, A.: Rossi, R. A. J. Org. Chem. 2004, 69, 2037-2041.
-
(2004)
J. Org. Chem
, vol.69
, pp. 2037-2041
-
-
Vaillard, S.E.1
Postigo, A.2
Rossi, R.A.3
-
13
-
-
24744468986
-
-
(c) Liu, Q.; Han, B.; Zhang, W.; Yang, L.; Liu, Z.-L.; Yu, W. Synlett 2005, 2248-2250.
-
(2005)
Synlett
, pp. 2248-2250
-
-
Liu, Q.1
Han, B.2
Zhang, W.3
Yang, L.4
Liu, Z.-L.5
Yu, W.6
-
17
-
-
0001360724
-
-
-1 for the 5-exo-cyclization of 2-(allyloxy)phenyl radicals: Johnston, L. J.; Lusztyk, J.; Wayner, D. D. M.; Abeywickreyma, A. N.; Beckwith, A. L. J.; Scaiano, J. C.; Ingold, K. U. J. Am. Chem. Soc. 1985, 107, 4594-4596.
-
-1 for the 5-exo-cyclization of 2-(allyloxy)phenyl radicals: Johnston, L. J.; Lusztyk, J.; Wayner, D. D. M.; Abeywickreyma, A. N.; Beckwith, A. L. J.; Scaiano, J. C.; Ingold, K. U. J. Am. Chem. Soc. 1985, 107, 4594-4596.
-
-
-
-
18
-
-
33746877486
-
-
(a) Heinrich, M. R.; Blank, O.; Wölfel, S. Org. Lett. 2006, 8, 3323-3325.
-
(2006)
Org. Lett
, vol.8
, pp. 3323-3325
-
-
Heinrich, M.R.1
Blank, O.2
Wölfel, S.3
-
19
-
-
33846204009
-
-
(b) Heinrich, M. R.; Blank, O.; Wetzel, A. J. Org. Chem. 2007, 72, 476-484.
-
(2007)
J. Org. Chem
, vol.72
, pp. 476-484
-
-
Heinrich, M.R.1
Blank, O.2
Wetzel, A.3
-
20
-
-
0035781106
-
-
For alkoxyamines as regulators for living polymerizations, see
-
For alkoxyamines as regulators for living polymerizations, see: Hawker, C. J.; Bosman, A. W.; Hart, E. Chem. Rev. 2001, 101, 3661-3688.
-
(2001)
Chem. Rev
, vol.101
, pp. 3661-3688
-
-
Hawker, C.J.1
Bosman, A.W.2
Hart, E.3
-
21
-
-
84944203602
-
-
For the decomposition of dibenzoyl peroxide in the presence of olefins and TEMPO, see
-
For the decomposition of dibenzoyl peroxide in the presence of olefins and TEMPO, see: Moad, G.; Rizzardo, E.; Solomon, D. H. Aust. J. Chem. 1983, 36, 1573-1588.
-
(1983)
Aust. J. Chem
, vol.36
, pp. 1573-1588
-
-
Moad, G.1
Rizzardo, E.2
Solomon, D.H.3
-
22
-
-
34247165162
-
-
For a recent report on the organocatalytic radical α-oxygenation of aldehydes involving TEMPO as trapping reagent, see: Sibi, M. P, Hasegawa, M. J. Am. Chem. Soc. 2007, 129, 4124-412
-
For a recent report on the organocatalytic radical α-oxygenation of aldehydes involving TEMPO as trapping reagent, see: Sibi, M. P.; Hasegawa, M. J. Am. Chem. Soc. 2007, 129, 4124-412.
-
-
-
-
23
-
-
33344460519
-
-
For the photochemical formation of aryl radicals in the presence of TEMPO, see
-
For the photochemical formation of aryl radicals in the presence of TEMPO, see: Heinrich, M. R.; Kirschstein, M. Tetrahedron Lett. 2006, 47, 2115-2118.
-
(2006)
Tetrahedron Lett
, vol.47
, pp. 2115-2118
-
-
Heinrich, M.R.1
Kirschstein, M.2
-
24
-
-
0002200501
-
-
-1 (5 °C): Citterio, A.; Minisci, F.; Vismara, E. J. Org. Chem. 1982, 47, 81-88.
-
-1 (5 °C): Citterio, A.; Minisci, F.; Vismara, E. J. Org. Chem. 1982, 47, 81-88.
-
-
-
-
25
-
-
0000955889
-
-
Garden, S. J.; Avila, D. V.; Beckwith, A. L. J.; Bowry, V. W.; Ingold, K. U.; Lusztyk, J. J. Org. Chem. 1996, 61, 805-809.
-
(1996)
J. Org. Chem
, vol.61
, pp. 805-809
-
-
Garden, S.J.1
Avila, D.V.2
Beckwith, A.L.J.3
Bowry, V.W.4
Ingold, K.U.5
Lusztyk, J.6
-
26
-
-
0000745524
-
-
For kinetics of nitroxide radical trapping solvent, effects, see
-
For kinetics of nitroxide radical trapping (solvent, effects), see: Beckwith, A. L. J.; Bowry, V. W.; Ingold, K. U. J. Am. Chem. Soc. 1992, 114, 4983-4992.
-
(1992)
J. Am. Chem. Soc
, vol.114
, pp. 4983-4992
-
-
Beckwith, A.L.J.1
Bowry, V.W.2
Ingold, K.U.3
-
27
-
-
0034678011
-
-
For carboaminohydroxylation, see: a
-
For carboaminohydroxylation, see: (a) Studer, A. Angew. Chem., Int. Ed. 2000, 39, 1108-1111.
-
(2000)
Angew. Chem., Int. Ed
, vol.39
, pp. 1108-1111
-
-
Studer, A.1
-
28
-
-
0141855228
-
-
(b) Wetter, C.; Jantos, K.; Woithe, K.; Studer, A. Org. Lett. 2003, 5, 2899-2902.
-
(2003)
Org. Lett
, vol.5
, pp. 2899-2902
-
-
Wetter, C.1
Jantos, K.2
Woithe, K.3
Studer, A.4
-
32
-
-
0035781101
-
-
For the persistant radical effect (PRE), see: (a) Fischer, H. Chem. Rev. 2001, 101, 3581-3610.
-
For the persistant radical effect (PRE), see: (a) Fischer, H. Chem. Rev. 2001, 101, 3581-3610.
-
-
-
-
33
-
-
0035896265
-
-
(b) Studer, A. Chem. Eur. J. 2001, 7, 1159-1164.
-
(2001)
Chem. Eur. J
, vol.7
, pp. 1159-1164
-
-
Studer, A.1
-
36
-
-
34848893565
-
-
4. Concentration and purification by column chromatography furnished the carboaminohydroxylation products.
-
4. Concentration and purification by column chromatography furnished the carboaminohydroxylation products.
-
-
-
-
37
-
-
0042004947
-
-
Electrophilic radicals (e.g., in the a-position of a carbonyl, ester, or cyano group) are unreactive toward diazonium salts: (a) Minisci, F.; Coppa, F.; Fontana, F.; Pianese, G.; Zhao, L. J. Org. Chem. 1992, 57, 3929-3933.
-
Electrophilic radicals (e.g., in the a-position of a carbonyl, ester, or cyano group) are unreactive toward diazonium salts: (a) Minisci, F.; Coppa, F.; Fontana, F.; Pianese, G.; Zhao, L. J. Org. Chem. 1992, 57, 3929-3933.
-
-
-
-
39
-
-
0032528238
-
-
For recent reports on nonradical carbohydroxylation, see: a
-
For recent reports on nonradical carbohydroxylation, see: (a) Nakamura, H.; Sekido, M.; Ito, M.; Yamamoto, Y. J. Am. Chem. Soc. 1998, 120, 6838-6839.
-
(1998)
J. Am. Chem. Soc
, vol.120
, pp. 6838-6839
-
-
Nakamura, H.1
Sekido, M.2
Ito, M.3
Yamamoto, Y.4
-
41
-
-
0038081446
-
-
(c) Fürstner, A.; Szillat, H.; Stelzer, F. J. Am. Chem. Soc. 2000, 122, 6785-6786.
-
(2000)
J. Am. Chem. Soc
, vol.122
, pp. 6785-6786
-
-
Fürstner, A.1
Szillat, H.2
Stelzer, F.3
-
42
-
-
4344621693
-
-
(d) Suga, S.; Kageyama, Y.; Babu, G.; Itami, K.; Yoshida, J. Org. Lett. 2004, 6, 2709-2711.
-
(2004)
Org. Lett
, vol.6
, pp. 2709-2711
-
-
Suga, S.1
Kageyama, Y.2
Babu, G.3
Itami, K.4
Yoshida, J.5
-
43
-
-
0742304172
-
-
(e) Miller, S. P.; Morgan, J. P.; Nepveux, F. J., V; Morken, J. P. Org. Lett. 2004, 6, 131-133.
-
(2004)
Org. Lett
, vol.6
, pp. 131-133
-
-
Miller, S.P.1
Morgan, J.P.2
Nepveux, F.J.V.3
Morken, J.P.4
-
45
-
-
33846064261
-
-
(a) Wang, K.-J.; Zhang, Y.-J.; Yang, C.-R. Chem. Biodiversity 2006, 3, 1317-1324.
-
(2006)
Chem. Biodiversity
, vol.3
, pp. 1317-1324
-
-
Wang, K.-J.1
Zhang, Y.-J.2
Yang, C.-R.3
-
46
-
-
3543151359
-
-
(b) Zhang, Y.-J.; Nagao, T.; Tanaka, T.; Yang, C.-R.; Okabe, H.; Kouno, I. Biol. Pharm. Bull. 2004, 27, 251-255.
-
(2004)
Biol. Pharm. Bull
, vol.27
, pp. 251-255
-
-
Zhang, Y.-J.1
Nagao, T.2
Tanaka, T.3
Yang, C.-R.4
Okabe, H.5
Kouno, I.6
|