-
1
-
-
0242526099
-
-
For recent reviews on C-H activation and functionalization, see: (a)
-
For recent reviews on C-H activation and functionalization, see: (a) Kakiuchi, F.; Chatani, N. Adv. Synth. Catal. 2003, 345, 1077.
-
(2003)
Adv. Synth. Catal.
, vol.345
, pp. 1077
-
-
Kakiuchi, F.1
Chatani, N.2
-
2
-
-
0036589261
-
-
(b) Ritleng, V.; Sirlin, C.; Pfeffer, M. Chem. Rev. 2002, 102, 1731.
-
(2002)
Chem. Rev.
, vol.102
, pp. 1731
-
-
Ritleng, V.1
Sirlin, C.2
Pfeffer, M.3
-
3
-
-
65249146649
-
-
For recent reviews on activation of sp3 C-H bonds adjacent to a nitrogen atom, see: (a)
-
For recent reviews on activation of sp3 C-H bonds adjacent to a nitrogen atom, see: (a) Li, C. J. Acc. Chem. Res. 2009, 42, 335.
-
(2009)
Acc. Chem. Res.
, vol.42
, pp. 335
-
-
Li, C.J.1
-
11
-
-
0001039632
-
-
(a) Shono, T.; Matsumura, Y.; Onomura, O.; Ogaki, M.; Kanazawa, T. J. Org. Chem. 1987, 52, 536.
-
(1987)
J. Org. Chem.
, vol.52
, pp. 536
-
-
Shono, T.1
Matsumura, Y.2
Onomura, O.3
Ogaki, M.4
Kanazawa, T.5
-
14
-
-
0000588796
-
-
(d) Shono, T.; Hamaguchi, H.; Matsumura, Y. J. Am. Chem. Soc. 1975, 97, 4264.
-
(1975)
J. Am. Chem. Soc.
, vol.97
, pp. 4264
-
-
Shono, T.1
Hamaguchi, H.2
Matsumura, Y.3
-
16
-
-
0037077015
-
-
(a) Sun, P.; Sun, C.; Weinreb, S. M. J. Org. Chem. 2002, 67, 4337.
-
(2002)
J. Org. Chem.
, vol.67
, pp. 4337
-
-
Sun, P.1
Sun, C.2
Weinreb, S.M.3
-
17
-
-
0001594575
-
-
(b) Han, G.; LaPorte, M.; McIntosh, M. C.; Weinreb, S. M. J. Org. Chem. 1996, 61, 9483.
-
(1996)
J. Org. Chem.
, vol.61
, pp. 9483
-
-
Han, G.1
LaPorte, M.2
McIntosh, M.C.3
Weinreb, S.M.4
-
18
-
-
0026450952
-
-
(a) Murahashi, S.-I.; Naota, T.; Miyaguchi, N.; Nakato, T. Tetrahedron Lett. 1992, 33, 6991.
-
(1992)
Tetrahedron Lett.
, vol.33
, pp. 6991
-
-
Murahashi, S.-I.1
Naota, T.2
Miyaguchi, N.3
Nakato, T.4
-
19
-
-
0026072907
-
-
(b) Murahashi, S.-I.; Saito, T.; Naota, T.; Kumobakashi, H.; Akutogaua, S. Tetrahedron Lett. 1991, 32, 5991.
-
(1991)
Tetrahedron Lett.
, vol.32
, pp. 5991
-
-
Murahashi, S.-I.1
Saito, T.2
Naota, T.3
Kumobakashi, H.4
Akutogaua, S.5
-
20
-
-
0025760728
-
-
(c) Murahashi, S.-I.; Saito, T.; Naota, T.; Kumobayashi, H.; Akutapxwa, S. Tetrahedron Lett. 1991, 32, 2145.
-
(1991)
Tetrahedron Lett.
, vol.32
, pp. 2145
-
-
Murahashi, S.-I.1
Saito, T.2
Naota, T.3
Kumobayashi, H.4
Akutapxwa, S.5
-
21
-
-
0000687399
-
-
(d) Murahashi, S.-I.; Naota, T.; Kuwzbara, T.; Saito, T.; Kumobayashi, H.; Akutagawa, S. J. Am. Chem. Soc. 1990, 1l2, 7820.
-
(1990)
J. Am. Chem. Soc.
, vol.1 L2
, pp. 7820
-
-
Murahashi, S.-I.1
Naota, T.2
Kuwzbara, T.3
Saito, T.4
Kumobayashi, H.5
Akutagawa, S.6
-
22
-
-
0000638447
-
-
(e) Murahashi, S.-I.; Naota, T.; Yonemura, K. J. Am. Chem. Soc. 1988, 110, 8256.
-
(1988)
J. Am. Chem. Soc.
, vol.110
, pp. 8256
-
-
Murahashi, S.-I.1
Naota, T.2
Yonemura, K.3
-
23
-
-
33746872900
-
-
(a) Reddy, B. V. S.; Reddy, L. R.; Corey, E. J. Org. Lett. 2006, 8, 3391.
-
(2006)
Org. Lett.
, vol.8
, pp. 3391
-
-
Reddy, B.V.S.1
Reddy, L.R.2
Corey, E.J.3
-
24
-
-
33746918323
-
-
(b) Wang, D.-H.; Hao, X.-S.; Wu, D.-F.; Yu, J.-Q. Org. Lett. 2006, 8, 3387.
-
(2006)
Org. Lett.
, vol.8
, pp. 3387
-
-
Wang, D.-H.1
Hao, X.-S.2
Wu, D.-F.3
Yu, J.-Q.4
-
25
-
-
70349463744
-
-
note
-
The only example was achieved by electrochemical oxidation, see ref 3a.
-
-
-
-
26
-
-
33845280103
-
-
(a) Jacobsen, E. N.; Markó, I.; Mungall, W. S.; Schröder, G.; Sharpless, K. B. J. Am. Chem. Soc. 1988, 110, 1968.
-
(1988)
J. Am. Chem. Soc.
, vol.110
, pp. 1968
-
-
Jacobsen, E.N.1
Markó, I.2
Mungall, W.S.3
Schröder, G.4
Sharpless, K.B.5
-
27
-
-
0003544583
-
-
Ojima, Ed.; VCH: New York
-
(b) Johnson, R. A.; Sharpless, K. B. In Catalytic Asymmetric Synthesis, 2nd ed.; Ojima, I., Ed.; VCH: New York, 2000.
-
(2000)
Catalytic Asymmetric Synthesis, 2nd Ed.
, vol.1
-
-
Johnson, R.A.1
Sharpless, K.B.2
-
28
-
-
0042021461
-
-
For Fe-catalyzed dihydroxylations: (a)
-
For Fe-catalyzed dihydroxylations: (a) Fujita, M.; Costas, M.; Que, L., Jr. J. Am. Chem. Soc. 2003, 125, 9912.
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 9912
-
-
Fujita, M.1
Costas, M.2
Que Jr., L.3
-
29
-
-
0037181365
-
-
(b) Chen, K.; Costas, M.; Kim, J.; Tipton, A. K.; Que, L., Jr. J. Am. Chem. Soc. 2002, 124, 3026.
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 3026
-
-
Chen, K.1
Costas, M.2
Kim, J.3
Tipton, A.K.4
Que Jr., L.5
-
30
-
-
0345583676
-
-
(c) Chen, K.; Que, L. Angew. Chem., Int. Ed. 1999, 38, 2227.
-
(1999)
Angew. Chem., Int. Ed.
, vol.38
, pp. 2227
-
-
Chen, K.1
Que, L.2
-
31
-
-
0036532292
-
-
For Mn-catalyzed dihydroxylations: (d)
-
For Mn-catalyzed dihydroxylations: (d) Brinksma, J.; Schmieder, L.; Van Vliet, G.; Boaron, R.; Hage, R.; De Vos, D. E.; Alsters, P. L.; Feringa, B. L. Tetrahedron Lett. 2002, 43, 2619.
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 2619
-
-
Brinksma, J.1
Schmieder, L.2
Van Vliet, G.3
Boaron, R.4
Hage, R.5
De Vos, D.E.6
Alsters, P.L.7
Feringa, B.L.8
-
32
-
-
0033119499
-
-
(e) De Vos, D. E.; De Wildeman, S.; Sels, B. F.; Grobet, P. J.; Jacobs, P. A. Angew. Chem., Int. Ed. 1999, 38, 980.
-
(1999)
Angew. Chem., Int. Ed.
, vol.38
, pp. 980
-
-
De Vos, D.E.1
De Wildeman, S.2
Sels, B.F.3
Grobet, P.J.4
Jacobs, P.A.5
-
33
-
-
26844562589
-
-
For Ru-catalyzed dihydroxylations: (f)
-
For Ru-catalyzed dihydroxylations: (f) Yip, W.-P.; Yu, W.-Y.; Zhu, N.; Che, C.-M. J. Am. Chem. Soc. 2005, 127, 14239.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 14239
-
-
Yip, W.-P.1
Yu, W.-Y.2
Zhu, N.3
Che, C.-M.4
-
34
-
-
4644293702
-
-
(g) Ho, C.-M.; Yu, W.-Y.; Che, C.-M. Angew. Chem., Int. Ed. 2004, 43, 3303.
-
(2004)
Angew. Chem., Int. Ed.
, vol.43
, pp. 3303
-
-
Ho, C.-M.1
Yu, W.-Y.2
Che, C.-M.3
-
36
-
-
33748225303
-
-
(i) Shing, T. K. M.; Tai, V. W. F.; Tam, E. K. W. Angew. Chem., Int. Ed. 1994, 33, 2312.
-
(1994)
Angew. Chem., Int. Ed.
, vol.33
, pp. 2312
-
-
Shing, T.K.M.1
Tai, V.W.F.2
Tam, E.K.W.3
-
37
-
-
67749110109
-
-
For Pdcatalyzed dihydroxylations: (j)
-
For Pdcatalyzed dihydroxylations: (j)Wang, A.; Jiang, H.; Chen, H. J. Am. Chem. Soc. 2009, 131, 3846.
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 3846
-
-
Wang, A.1
Jiang, H.2
Chen, H.3
-
39
-
-
33646083667
-
-
Celik, M.; Alp, C.; Coskun, B.; Gültekina, M. S.; Balci, M. Tetrahedron Lett. 2006, 47, 3659.
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 3659
-
-
Celik, M.1
Alp, C.2
Coskun, B.3
Gültekina, M.S.4
Balci, M.5
-
40
-
-
34249012488
-
-
HH (ax-ax, trans): 6-14 Hz]. The coupling constants of similar structure, such as (cis and trans)- 2,3-dihydroxypyrans and substituted tetrahydroquinoline, can also be used for reference. For detail, see: (a)
-
HH (ax-ax, trans): 6-14 Hz]. The coupling constants of similar structure, such as (cis and trans)- 2,3-dihydroxypyrans and substituted tetrahydroquinoline, can also be used for reference. For detail, see: (a) Levecque, P.; Gammon, D.; Kinfe, H. H.; Jacobs, P.; De Vos, D.; Sels, B. Org. Biomol. Chem. 2007, 5, 1800.
-
(2007)
Org. Biomol. Chem.
, vol.5
, pp. 1800
-
-
Levecque, P.1
Gammon, D.2
Kinfe, H.H.3
Jacobs, P.4
De Vos, D.5
Sels, B.6
-
41
-
-
0029933876
-
-
(b) Sugai, T.; lkeda, H.; Ohta, H. Tetrahedron 1996, 52, 8123.
-
(1996)
Tetrahedron
, vol.52
, pp. 8123
-
-
Sugai, T.1
Lkeda, H.2
Ohta, H.3
-
42
-
-
33845335853
-
-
(c) Sridharan, V.; Avendaño, C.; Menéndez, J. C. Tetrahedron 2007, 63, 673.
-
(2007)
Tetrahedron
, vol.63
, pp. 673
-
-
Sridharan, V.1
Avendaño, C.2
Menéndez, J.C.3
-
43
-
-
0001636945
-
-
Furthermore, hypervalent iodine(III) reagents promoted dioxygenation of alkenes always afford the cis-products. The mechanism of the formation of the cis-products have been proposed before. For detail, see (d) Also see ref 11
-
Furthermore, hypervalent iodine(III) reagents promoted dioxygenation of alkenes always afford the cis-products. The mechanism of the formation of the cis-products have been proposed before. For detail, see (d) Rebrovic, L.; Koser, G. F. J. Org. Chem. 1984, 49, 2462. Also see ref 11.
-
(1984)
J. Org. Chem.
, vol.49
, pp. 2462
-
-
Rebrovic, L.1
Koser, G.F.2
-
44
-
-
50249118196
-
-
(a) Murahashi, S.-I.; Nakae, T.; Terai, H.; Komiya, N. J. Am. Chem. Soc. 2008, 130, 11005.
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 11005
-
-
Murahashi, S.-I.1
Nakae, T.2
Terai, H.3
Komiya, N.4
-
45
-
-
27544488753
-
-
(b) Murahashi, S.; Komiya, N.; Terai, H. Angew. Chem., Int. Ed. 2005, 44, 6931.
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 6931
-
-
Murahashi, S.1
Komiya, N.2
Terai, H.3
-
46
-
-
0346850026
-
-
(c) Murahashi, S.; Komiya, N.; Terai, H.; Nakae, T. J. Am. Chem. Soc. 2003, 125, 15312.
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 15312
-
-
Murahashi, S.1
Komiya, N.2
Terai, H.3
Nakae, T.4
-
47
-
-
33646559970
-
-
Catino, A. J.; Nichols, J. M.; Nettles, B. J.; Doyle, M. P. J. Am. Chem. Soc. 2006, 128, 5648.
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 5648
-
-
Catino, A.J.1
Nichols, J.M.2
Nettles, B.J.3
Doyle, M.P.4
-
48
-
-
54749113948
-
-
For select examples, see: (a)
-
For select examples, see: (a) Zhao, L.; Li, C.-J. Angew. Chem., Int. Ed. 2008, 47, 7075.
-
(2008)
Angew. Chem., Int. Ed.
, vol.47
, pp. 7075
-
-
Zhao, L.1
Li, C.-J.2
-
51
-
-
33745157509
-
-
(d) Li, Z.; Bohle, D. S.; Li, C.-J. Proc. Natl. Acad. Sci. U.S.A. 2006, 103, 8928.
-
(2006)
Proc. Natl. Acad. Sci. U.S.A.
, vol.103
, pp. 8928
-
-
Li, Z.1
Bohle, D.S.2
Li, C.-J.3
-
58
-
-
66149114375
-
-
(b) Chu, L. L.; Zhang, X. G.; Qing, F.-L. Org. Lett. 2009, 11, 2197.
-
(2009)
Org. Lett.
, vol.11
, pp. 2197
-
-
Chu, L.L.1
Zhang, X.G.2
Qing, F.-L.3
-
61
-
-
61449212055
-
-
(e) Shen, Y.-M.; Li, M.; Wang, S.-Z.; Zhan, T.-G.; Tan, Z.; Guo, C.-C. Chem.Commun. 2009, 8, 953.
-
(2009)
Chem.Commun.
, vol.8
, pp. 953
-
-
Shen, Y.-M.1
Li, M.2
Wang, S.-Z.3
Zhan, T.-G.4
Tan, Z.5
Guo, C.-C.6
-
62
-
-
34848918499
-
-
(f) Zhang, Y.; Fu, H.; Jiang, Y.; Zhao, Y.-F. Org. Lett. 2007, 19, 3813.
-
(2007)
Org. Lett.
, vol.19
, pp. 3813
-
-
Zhang, Y.1
Fu, H.2
Jiang, Y.3
Zhao, Y.-F.4
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