-
1
-
-
79952675758
-
-
For a review on iron-promoted reactions involving C-H bond functionalization, see.
-
For a review on iron-promoted reactions involving C-H bond functionalization, see:, C.-L. Sun, B.-J. Li, Z.-J. Shi, Chem. Rev. 2011, 111, 1293-1314.
-
(2011)
Chem. Rev.
, vol.111
, pp. 1293-1314
-
-
Sun, C.-L.1
Li, B.-J.2
Shi, Z.-J.3
-
2
-
-
84871051155
-
-
3-C-H bonds, see
-
3-C-H bonds, see
-
-
-
-
5
-
-
84871097172
-
-
Ed.
-
R. H. Crabtree, Ed. Chem. Rev. 2010, 110, 576-1211
-
(2010)
Chem. Rev.
, vol.110
, pp. 576-1211
-
-
Crabtree, R.H.1
-
7
-
-
78650648241
-
-
M. Wasa, K. M. Engle, J.-Q. Yu, Isr. J. Chem. 2010, 50, 605-616
-
(2010)
Isr. J. Chem.
, vol.50
, pp. 605-616
-
-
Wasa, M.1
Engle, K.M.2
Yu, J.-Q.3
-
8
-
-
77349125577
-
-
I. A. I. Mkhalid, J. H. Barnard, T. B. Marder, J. M. Murphy, J. F. Hartwig, Chem. Rev. 2010, 110, 890-931
-
(2010)
Chem. Rev.
, vol.110
, pp. 890-931
-
-
Mkhalid, I.A.I.1
Barnard, J.H.2
Marder, T.B.3
Murphy, J.M.4
Hartwig, J.F.5
-
9
-
-
77149164746
-
-
R. Jazzar, J. Hitce, A. Renaudat, J. Sofack-Kreutzer, O. Baudoin, Chem. Eur. J. 2010, 16, 2654-2672
-
(2010)
Chem. Eur. J.
, vol.16
, pp. 2654-2672
-
-
Jazzar, R.1
Hitce, J.2
Renaudat, A.3
Sofack-Kreutzer, J.4
Baudoin, O.5
-
10
-
-
84855398195
-
-
T. A. Ramirez, B. Zhao, Y. Shi, Chem. Soc. Rev. 2012, 41, 931-942.
-
(2012)
Chem. Soc. Rev.
, vol.41
, pp. 931-942
-
-
Ramirez, T.A.1
Zhao, B.2
Shi, Y.3
-
11
-
-
84871102578
-
-
2H has been reported. Under Fe catalysis
-
2H has been reported. Under Fe catalysis
-
-
-
-
12
-
-
0026675484
-
-
D. H. R. Barton, S. D. Bévière, W. Chavasiri, D. Doller, B. Hu, Tetrahedron Lett. 1992, 33, 5473-5476
-
(1992)
Tetrahedron Lett.
, vol.33
, pp. 5473-5476
-
-
Barton, D.H.R.1
Bévière, S.D.2
Chavasiri, W.3
Doller, D.4
Hu, B.5
-
13
-
-
79960252042
-
-
W. Liu, Y. Li, K. Liu, Z. Li, J. Am. Chem. Soc. 2011, 133, 10756-10759
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 10756-10759
-
-
Liu, W.1
Li, Y.2
Liu, K.3
Li, Z.4
-
16
-
-
0027530711
-
-
S.-I. Murahashi, Y. Oda, T. Naota, T. Kuwabara, Tetrahedron Lett. 1993, 34, 1299-1302
-
(1993)
Tetrahedron Lett.
, vol.34
, pp. 1299-1302
-
-
Murahashi, S.-I.1
Oda, Y.2
Naota, T.3
Kuwabara, T.4
-
18
-
-
0000638447
-
-
Cu
-
S.-I. Murahashi, T. Naota, K. Yonemura, J. Am. Chem. Soc. 1988, 110, 8256-8258. Cu
-
(1988)
J. Am. Chem. Soc.
, vol.110
, pp. 8256-8258
-
-
Murahashi, S.-I.1
Naota, T.2
Yonemura, K.3
-
20
-
-
84871089350
-
-
2H has been also documented. Under Fe catalysis
-
2H has been also documented. Under Fe catalysis
-
-
-
-
22
-
-
28244482843
-
-
Metal-free
-
A. J. Catino, J. M. Nichols, H. Choi, S. Gottipamula, M. P. Doyle, Org. Lett. 2005, 7, 5167-5170. Metal-free
-
(2005)
Org. Lett.
, vol.7
, pp. 5167-5170
-
-
Catino, A.J.1
Nichols, J.M.2
Choi, H.3
Gottipamula, S.4
Doyle, M.P.5
-
23
-
-
71549150337
-
-
J. Zhang, Z. Wang, Y. Wang, C. Wan, X. Zheng, Z. Wang, Green Chem. 2009, 11, 1973-1978
-
(2009)
Green Chem.
, vol.11
, pp. 1973-1978
-
-
Zhang, J.1
Wang, Z.2
Wang, Y.3
Wan, C.4
Zheng, X.5
Wang, Z.6
-
24
-
-
0029840740
-
-
M. Ochiai, T. Ito, H. Takahashi, A. Nakanishi, M. Toyonari, T. Sueda, S. Goto, M. Shiro, J. Am. Chem. Soc. 1996, 118, 7716-7730
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 7716-7730
-
-
Ochiai, M.1
Ito, T.2
Takahashi, H.3
Nakanishi, A.4
Toyonari, M.5
Sueda, T.6
Goto, S.7
Shiro, M.8
-
25
-
-
0000579758
-
-
T. Sueda, S. Fukuda, M. Ochiai, Org. Lett. 2001, 3, 2387-2390.
-
(2001)
Org. Lett.
, vol.3
, pp. 2387-2390
-
-
Sueda, T.1
Fukuda, S.2
Ochiai, M.3
-
26
-
-
84871099792
-
-
2H as stoichiometric oxidant, see the followings. Fe-promoted reactions
-
2H as stoichiometric oxidant, see the followings. Fe-promoted reactions
-
-
-
-
27
-
-
59049103808
-
-
Z. Li, R. Yu, H. Li, Angew. Chem. 2008, 120, 7607-7610
-
(2008)
Angew. Chem.
, vol.120
, pp. 7607-7610
-
-
Li, Z.1
Yu, R.2
Li, H.3
-
28
-
-
54749149062
-
-
Angew. Chem. Int. Ed. 2008, 47, 7497-7500
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 7497-7500
-
-
-
29
-
-
70349120945
-
-
H. Li, Z. He, X. Guo, W. Li, X. Zhao, Z. Li, Org. Lett. 2009, 11, 4176-4179
-
(2009)
Org. Lett.
, vol.11
, pp. 4176-4179
-
-
Li, H.1
He, Z.2
Guo, X.3
Li, W.4
Zhao, X.5
Li, Z.6
-
30
-
-
77951857209
-
-
S. Pan, J. Liu, H. Li, Z. Wang, X. Guo, Z. Li, Org. Lett. 2010, 12, 1932-1935
-
(2010)
Org. Lett.
, vol.12
, pp. 1932-1935
-
-
Pan, S.1
Liu, J.2
Li, H.3
Wang, Z.4
Guo, X.5
Li, Z.6
-
31
-
-
82355160856
-
-
W. Liu, J. Liu, D. Ogawa, Y. Nishihara, X. Guo, Z. Li, Org. Lett. 2011, 13, 6272-6275
-
(2011)
Org. Lett.
, vol.13
, pp. 6272-6275
-
-
Liu, W.1
Liu, J.2
Ogawa, D.3
Nishihara, Y.4
Guo, X.5
Li, Z.6
-
32
-
-
80052714613
-
-
Q. Xia, W. Chen, H. Qiu, J. Org. Chem. 2011, 76, 7577-7582
-
(2011)
J. Org. Chem.
, vol.76
, pp. 7577-7582
-
-
Xia, Q.1
Chen, W.2
Qiu, H.3
-
33
-
-
80055077308
-
-
M. Ghobrial, M. Schnürch, M. D. Mihovilovic, J. Org. Chem. 2011, 76, 8781-8793
-
(2011)
J. Org. Chem.
, vol.76
, pp. 8781-8793
-
-
Ghobrial, M.1
Schnürch, M.2
Mihovilovic, M.D.3
-
34
-
-
77954808623
-
-
Rh
-
W. Han, P. Mayer, A. R. Ofial, Adv. Synth. Catal. 2010, 352, 1667-1676. Rh
-
(2010)
Adv. Synth. Catal.
, vol.352
, pp. 1667-1676
-
-
Han, W.1
Mayer, P.2
Ofial, A.R.3
-
36
-
-
27144547547
-
-
Cu
-
Y. Bonvin, E. Callens, I. Larrosa, D. A. Henderson, J. Oldham, A. J. Burton, A. G. M. Barrett, Org. Lett. 2005, 7, 4549-4552. Cu
-
(2005)
Org. Lett.
, vol.7
, pp. 4549-4552
-
-
Bonvin, Y.1
Callens, E.2
Larrosa, I.3
Henderson, D.A.4
Oldham, J.5
Burton, A.J.6
Barrett, A.G.M.7
-
38
-
-
33745157509
-
-
Z. Li, D. S. Bohle, C.-J. Li, Proc. Natl. Acad. Sci. USA 2006, 103, 8928-8933
-
(2006)
Proc. Natl. Acad. Sci. USA
, vol.103
, pp. 8928-8933
-
-
Li, Z.1
Bohle, D.S.2
Li, C.-J.3
-
39
-
-
34848918499
-
-
Y. Zhang, H. Fu, Y. Jiang, Y. Zhao, Org. Lett. 2007, 9, 3813-3816
-
(2007)
Org. Lett.
, vol.9
, pp. 3813-3816
-
-
Zhang, Y.1
Fu, H.2
Jiang, Y.3
Zhao, Y.4
-
42
-
-
54749113948
-
-
Angew. Chem. Int. Ed. 2008, 47, 7075-7078
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 7075-7078
-
-
-
43
-
-
67649460736
-
-
K. Cheng, L. Huang, Y. Zhang, Org. Lett. 2009, 11, 2908-2911
-
(2009)
Org. Lett.
, vol.11
, pp. 2908-2911
-
-
Cheng, K.1
Huang, L.2
Zhang, Y.3
-
44
-
-
77957113130
-
-
X. Ye, C. Xie, Y. Pan, L. Han, T. Xie, Org. Lett. 2010, 12, 4240-4243
-
(2010)
Org. Lett.
, vol.12
, pp. 4240-4243
-
-
Ye, X.1
Xie, C.2
Pan, Y.3
Han, L.4
Xie, T.5
-
45
-
-
79953230911
-
-
Metal-free
-
Y. Wei, H. Ding, S. Lin, F. Liang, Org. Lett. 2011, 13, 1674-1677. Metal-free
-
(2011)
Org. Lett.
, vol.13
, pp. 1674-1677
-
-
Wei, Y.1
Ding, H.2
Lin, S.3
Liang, F.4
-
46
-
-
80054755679
-
-
T. He, L. Yu, L. Zhang, L. Wang, M. Wang, Org. Lett. 2011, 13, 5016-5019.
-
(2011)
Org. Lett.
, vol.13
, pp. 5016-5019
-
-
He, T.1
Yu, L.2
Zhang, L.3
Wang, L.4
Wang, M.5
-
48
-
-
84871061310
-
-
For reviews on iron-mediated or -catalyzed reactions, see
-
For reviews on iron-mediated or -catalyzed reactions, see
-
-
-
-
49
-
-
84890999876
-
-
(Ed.: B. Plietker), Wiley-VCH, Weinheim
-
Iron Catalysis in Organic Chemistry, (Ed.:, B. Plietker,), Wiley-VCH, Weinheim, 2008
-
(2008)
Iron Catalysis in Organic Chemistry
-
-
-
50
-
-
44349129755
-
-
A. Correa, O. G. Mancheño, C. Bolm, Chem. Soc. Rev. 2008, 37, 1108-1117
-
(2008)
Chem. Soc. Rev.
, vol.37
, pp. 1108-1117
-
-
Correa, A.1
Mancheño, O.G.2
Bolm, C.3
-
52
-
-
54849171100
-
-
S. Enthaler, K. Junge, M. Beller, Angew. Chem. 2008, 120, 3363-3367
-
(2008)
Angew. Chem.
, vol.120
, pp. 3363-3367
-
-
Enthaler, S.1
Junge, K.2
Beller, M.3
-
53
-
-
50049109778
-
-
Angew. Chem. Int. Ed. 2008, 47, 3317-3321
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 3317-3321
-
-
-
54
-
-
11144323895
-
-
For enyne cyclization, see
-
C. Bolm, J. Legros, J. Le Paih, L. Zani, Chem. Rev. 2004, 104, 6217-6254. For enyne cyclization, see
-
(2004)
Chem. Rev.
, vol.104
, pp. 6217-6254
-
-
Bolm, C.1
Legros, J.2
Le Paih, J.3
Zani, L.4
-
55
-
-
54849171800
-
-
V. Michelet, P. Y. Toullec, J.-P. Genêt, Angew. Chem. 2008, 120, 4338-4386
-
(2008)
Angew. Chem.
, vol.120
, pp. 4338-4386
-
-
Michelet, V.1
Toullec, P.Y.2
Genêt, J.-P.3
-
56
-
-
46649098072
-
-
For coupling reactions, see
-
Angew. Chem. Int. Ed. 2008, 47, 4268-4315. For coupling reactions, see
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 4268-4315
-
-
-
59
-
-
67649099463
-
-
W. M. Czaplik, M. Mayer, J. Cvengros, A. Jacobi von Wangelin, ChemSusChem 2009, 2, 396-417
-
(2009)
ChemSusChem
, vol.2
, pp. 396-417
-
-
Czaplik, W.M.1
Mayer, M.2
Cvengros, J.3
Von Wangelin, A.J.4
-
61
-
-
20444365340
-
-
For iron carbonyl complexes, see
-
A. Fürstner, R. Martin, Chem. Lett. 2005, 34, 624-629. For iron carbonyl complexes, see
-
(2005)
Chem. Lett.
, vol.34
, pp. 624-629
-
-
Fürstner, A.1
Martin, R.2
-
62
-
-
0004219714
-
-
in:, 2 nd edn., (Ed.: M. Schlosser), John Wiley & Sons, Chichester, pp
-
M. F. Semmelhack, in: Organometallics in Organic Synthesis. A Manual, 2 nd edn., (Ed.:, M. Schlosser,), John Wiley & Sons, Chichester, 2002, pp 1006-1121
-
(2002)
Organometallics in Organic Synthesis. A Manual
, pp. 1006-1121
-
-
Semmelhack, M.F.1
-
63
-
-
0003625966
-
-
4, (Eds.: G. Wilkinson, F. G. A. Stone, E. W. Abel), Pergamon Press, Oxford, ppâ€
-
Comprehensive Organometallic Chemistry, Vol. 4, (Eds.:, G. Wilkinson, F. G. A. Stone, E. W. Abel,), Pergamon Press, Oxford, 1982, pp 243-649.
-
(1982)
Comprehensive Organometallic Chemistry
, pp. 243-649
-
-
-
64
-
-
84871080877
-
-
For preparations of peroxyacetals and peroxyorthoesters, see the following: via C-H bond activation
-
For preparations of peroxyacetals and peroxyorthoesters, see the following: via C-H bond activation
-
-
-
-
65
-
-
84871066506
-
-
[3f]
-
[3f]
-
-
-
-
66
-
-
84871050483
-
-
[3g]; acetalization or acetal exchange
-
[3g]; acetalization or acetal exchange
-
-
-
-
67
-
-
84871035568
-
-
[4e]
-
[4e]
-
-
-
-
68
-
-
84871069957
-
-
[13e,f]
-
[13e,f]
-
-
-
-
69
-
-
84871093362
-
-
[14e]
-
[14e]
-
-
-
-
70
-
-
34547962666
-
-
K. Žmitek, M. Zupan, S. Stavber, J. Iskra, J. Org. Chem. 2007, 72, 6534-6540
-
(2007)
J. Org. Chem.
, vol.72
, pp. 6534-6540
-
-
Žmitek, K.1
Zupan, M.2
Stavber, S.3
Iskra, J.4
-
71
-
-
78649864359
-
-
ozonolysis
-
H.-J. Hamann, M. Hecht, A. Bunge, M. Gogol, J. Liebscher, Tetrahedron Lett. 2011, 52, 107-111; ozonolysis
-
(2011)
Tetrahedron Lett.
, vol.52
, pp. 107-111
-
-
Hamann, H.-J.1
Hecht, M.2
Bunge, A.3
Gogol, M.4
Liebscher, J.5
-
72
-
-
84871079019
-
-
[14a-d]; alkylation
-
[14a-d]; alkylation
-
-
-
-
74
-
-
84871078756
-
-
For our recent reports on synthetic application of oxygenation, see
-
For our recent reports on synthetic application of oxygenation, see
-
-
-
-
75
-
-
29844446598
-
-
Y. Nobe, K. Arayama, H. Urabe, J. Am. Chem. Soc. 2005, 127, 18006-18007
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 18006-18007
-
-
Nobe, Y.1
Arayama, K.2
Urabe, H.3
-
76
-
-
77949854901
-
-
H. Naito, T. Hata, H. Urabe, Org. Lett. 2010, 12, 1228-1230.
-
(2010)
Org. Lett.
, vol.12
, pp. 1228-1230
-
-
Naito, H.1
Hata, T.2
Urabe, H.3
-
77
-
-
84871041358
-
-
2H, see
-
2H, see
-
-
-
-
78
-
-
84871074151
-
-
[5c,f]
-
[5c,f]
-
-
-
-
80
-
-
0000031054
-
-
P. A. MacFaul, D. D. M. Wayner, K. U. Ingold, Acc. Chem. Res. 1998, 31, 159-162.
-
(1998)
Acc. Chem. Res.
, vol.31
, pp. 159-162
-
-
MacFaul, P.A.1
Wayner, D.D.M.2
Ingold, K.U.3
-
81
-
-
84871083038
-
-
2H by the Fe(II)-Fe(III) redox process. Subsequently, the former abstracts hydrogen from benzyl ether to give 15, which reacts with the latter to give the corresponding peroxyacetal. See
-
2H by the Fe(II)-Fe(III) redox process. Subsequently, the former abstracts hydrogen from benzyl ether to give 15, which reacts with the latter to give the corresponding peroxyacetal. See
-
-
-
-
82
-
-
84871070920
-
-
[3b,10b]
-
[3b,10b]
-
-
-
-
83
-
-
0030728024
-
-
P. A. MacFaul, K. U. Ingold, D. D. M. Wayner, L. Que Jr, J. Am. Chem. Soc. 1997, 119, 10594-10598.
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 10594-10598
-
-
MacFaul, P.A.1
Ingold, K.U.2
Wayner, D.D.M.3
Que Jr., J.4
-
84
-
-
0003787137
-
-
-, see:, John Wiley & Sons, Chichester, ppâ€
-
-, see:, I. Fleming, Frontier Orbitals and Organic Chemical Reactions, John Wiley & Sons, Chichester, 1976, pp 77-78.
-
(1976)
Frontier Orbitals and Organic Chemical Reactions
, pp. 77-78
-
-
Fleming, I.1
-
85
-
-
84871048429
-
-
Naturally occurring products containing peroxides are known. For a review, see
-
Naturally occurring products containing peroxides are known. For a review, see
-
-
-
-
87
-
-
0025778780
-
-
A. Nakamura, T. Ashino, M. Yamamoto, Tetrahedron Lett. 1991, 32, 4355-4358
-
(1991)
Tetrahedron Lett.
, vol.32
, pp. 4355-4358
-
-
Nakamura, A.1
Ashino, T.2
Yamamoto, M.3
-
88
-
-
0025987581
-
-
U. Anthoni, P. H. Nielsen, C. Christophersen, Tetrahedron Lett. 1991, 32, 7303-7304
-
(1991)
Tetrahedron Lett.
, vol.32
, pp. 7303-7304
-
-
Anthoni, U.1
Nielsen, P.H.2
Christophersen, C.3
-
89
-
-
0030976258
-
-
P. M. O'Neill, L. P. Bishop, N. L. Searle, J. L. Maggs, S. A. Ward, P. G. Bray, R. C. Storr, B. K. Park, Tetrahedron Lett. 1997, 38, 4263-4266
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 4263-4266
-
-
O'Neill, P.M.1
Bishop, L.P.2
Searle, N.L.3
Maggs, J.L.4
Ward, S.A.5
Bray, P.G.6
Storr, R.C.7
Park, B.K.8
-
90
-
-
0035829094
-
-
N. Murakami, M. Kawanishi, S. Itagaki, T. Horii, M. Kobayashi, Tetrahedron Lett. 2001, 42, 7281-7285
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 7281-7285
-
-
Murakami, N.1
Kawanishi, M.2
Itagaki, S.3
Horii, T.4
Kobayashi, M.5
-
91
-
-
0037033180
-
-
N. Murakami, M. Kawanishi, S. Itagaki, T. Horii, M. Kobayashi, Bioorg. Med. Chem. Lett. 2002, 12, 69-72.
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, pp. 69-72
-
-
Murakami, N.1
Kawanishi, M.2
Itagaki, S.3
Horii, T.4
Kobayashi, M.5
-
92
-
-
84871073199
-
-
For synthetic utility of peroxyacetals, see
-
For synthetic utility of peroxyacetals, see
-
-
-
-
93
-
-
0029993215
-
-
C. Helgorsky, A. Saux, M. Degueil-Castaing, B. Maillard, Tetrahedron 1996, 52, 8263-8274
-
(1996)
Tetrahedron
, vol.52
, pp. 8263-8274
-
-
Helgorsky, C.1
Saux, A.2
Degueil-Castaing, M.3
Maillard, B.4
-
94
-
-
0034661561
-
-
P. H. Dussault, R. J. Lee, J. A. Schultz, Y. S. Suh, Tetrahedron Lett. 2000, 41, 5457-5460
-
(2000)
Tetrahedron Lett.
, vol.41
, pp. 5457-5460
-
-
Dussault, P.H.1
Lee, R.J.2
Schultz, J.A.3
Suh, Y.S.4
-
95
-
-
0034680673
-
-
P. H. Dussault, T. K. Trullinger, S. Cho-Shultz, Tetrahedron 2000, 56, 9213-9220
-
(2000)
Tetrahedron
, vol.56
, pp. 9213-9220
-
-
Dussault, P.H.1
Trullinger, T.K.2
Cho-Shultz, S.3
-
96
-
-
0034670583
-
-
P. H. Dussault, I. Q. Lee, H.-J. Lee, R. J. Lee, Q. J. Niu, J. A. Schultz, U. R. Zope, J. Org. Chem. 2000, 65, 8407-8414
-
(2000)
J. Org. Chem.
, vol.65
, pp. 8407-8414
-
-
Dussault, P.H.1
Lee, I.Q.2
Lee, H.-J.3
Lee, R.J.4
Niu, Q.J.5
Schultz, J.A.6
Zope, U.R.7
-
99
-
-
84871082728
-
-
[3g]
-
[3g]
-
-
-
-
100
-
-
84871102904
-
-
2 group merely to give 2-hydroxyethyl benzoate in quantitative yield after aqueous work-up.
-
2 group merely to give 2-hydroxyethyl benzoate in quantitative yield after aqueous work-up.
-
-
-
|