-
1
-
-
0035232404
-
-
Ed, G. A. Cordell, Academic Press, San Diego
-
a) J. P. Michael in The Alkaloids, Vol. 55 (Ed.: G. A. Cordell), Academic Press, San Diego, 2001, pp. 91-258;
-
(2001)
The Alkaloids
, vol.55
, pp. 91-258
-
-
Michael, J.P.1
-
3
-
-
0038106171
-
-
c) R. Bloch, Chem. Rev. 1998, 98, 1407-1438;
-
(1998)
Chem. Rev
, vol.98
, pp. 1407-1438
-
-
Bloch, R.1
-
4
-
-
0001033542
-
-
d) G. Casiraghi, F. Zanardi, G. Rassu, P. Spanu, Chem. Rev. 1995, 95, 1677-1716.
-
(1995)
Chem. Rev
, vol.95
, pp. 1677-1716
-
-
Casiraghi, G.1
Zanardi, F.2
Rassu, G.3
Spanu, P.4
-
5
-
-
0000788623
-
-
For reviews, see: a
-
For reviews, see: a) T. E. Müller, M. Beller, Chem. Rev. 1998, 98, 675-703;
-
(1998)
Chem. Rev
, vol.98
, pp. 675-703
-
-
Müller, T.E.1
Beller, M.2
-
6
-
-
0003088944
-
-
Eds, A. Togni, H. Grützmacher, Wiley-VCH, New York
-
b) J. J. Brunet, D. Neibecker, Catalytic Heterofunctionalization (Eds.: A. Togni, H. Grützmacher), Wiley-VCH, New York, 2001, pp. 91-141;
-
(2001)
Catalytic Heterofunctionalization
, pp. 91-141
-
-
Brunet, J.J.1
Neibecker, D.2
-
9
-
-
34047161855
-
-
e) V. Kotov, C. C. Scarborough, S. S. Stahl, Inorg. Chem. 2007, 46, 1910-1923.
-
(2007)
Inorg. Chem
, vol.46
, pp. 1910-1923
-
-
Kotov, V.1
Scarborough, C.C.2
Stahl, S.S.3
-
10
-
-
0141954256
-
-
For other examples of catalytic amination of unactivated olefins, see: a
-
For other examples of catalytic amination of unactivated olefins, see: a) J.-S. Ryu, G. Y. Li, T. J. Marks, J. Am. Chem. Soc. 2003, 125, 12584-12605;
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 12584-12605
-
-
Ryu, J.-S.1
Li, G.Y.2
Marks, T.J.3
-
11
-
-
33244465401
-
-
b) J. Zhang, C.-G. Yang, C. He, J. Am. Chem. Soc. 2006, 128, 1798-1799;
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 1798-1799
-
-
Zhang, J.1
Yang, C.-G.2
He, C.3
-
12
-
-
34250863844
-
-
c) H. Du, W. Yuan, B. Zhao, Y. Shi, J. Am. Chem. Soc. 2007, 129, 7496-7497.
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 7496-7497
-
-
Du, H.1
Yuan, W.2
Zhao, B.3
Shi, Y.4
-
13
-
-
36849030278
-
-
For reviews that describe aerobic oxidative amination reactions, see: a
-
For reviews that describe aerobic oxidative amination reactions, see: a) E. M. Beccalli, G. Broggini, M. Martinelli, S. Sottocornola, Chem. Rev. 2007, 107, 5318-5365;
-
(2007)
Chem. Rev
, vol.107
, pp. 5318-5365
-
-
Beccalli, E.M.1
Broggini, G.2
Martinelli, M.3
Sottocornola, S.4
-
14
-
-
10044294415
-
-
b) S. S. Stahl, Angew. Chem. 2004, 116, 3480-3501;
-
(2004)
Angew. Chem
, vol.116
, pp. 3480-3501
-
-
Stahl, S.S.1
-
15
-
-
4143153074
-
-
Angew. Chem. Int. Ed. 2004, 43, 3400-3420.
-
(2004)
Angew. Chem. Int. Ed
, vol.43
, pp. 3400-3420
-
-
-
16
-
-
0026785465
-
-
For intermolecular aerobic oxidative amination of electron-deficient olefins, see: a
-
For intermolecular aerobic oxidative amination of electron-deficient olefins, see: a) T. Hosokawa, M. Takano, Y. Kuroki, S.-I. Murahashi, Tetrahedron Lett. 1992, 33, 6643-6646;
-
(1992)
Tetrahedron Lett
, vol.33
, pp. 6643-6646
-
-
Hosokawa, T.1
Takano, M.2
Kuroki, Y.3
Murahashi, S.-I.4
-
18
-
-
0142214634
-
-
For intermolecular aerobic oxidative amination, see: a
-
For intermolecular aerobic oxidative amination, see: a) V. I. Timokhin, N. R. Anastasi, S. S. Stahl, J. Am. Chem. Soc. 2003, 125, 12996-12997;
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 12996-12997
-
-
Timokhin, V.I.1
Anastasi, N.R.2
Stahl, S.S.3
-
19
-
-
14844317635
-
-
b) J. L. Brice, J. E. Harang, V. I. Timokhin, N. R. Anastasi, S. S. Stahl, J. Am. Chem. Soc. 2005, 127, 2868-2869;
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 2868-2869
-
-
Brice, J.L.1
Harang, J.E.2
Timokhin, V.I.3
Anastasi, N.R.4
Stahl, S.S.5
-
21
-
-
35548990249
-
-
d) M. M. Rogers, V. Kotov, J. Chatwichien, S. S. Stahl, Org. Lett. 2007, 9, 4331-4334.
-
(2007)
Org. Lett
, vol.9
, pp. 4331-4334
-
-
Rogers, M.M.1
Kotov, V.2
Chatwichien, J.3
Stahl, S.S.4
-
22
-
-
1042276609
-
-
For Pd-catalyzed allylic acetoxylation of terminal alkenes, see: a
-
For Pd-catalyzed allylic acetoxylation of terminal alkenes, see: a) M. S. Chen, M. C. White, J. Am. Chem. Soc. 2004, 126, 1346-1347;
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 1346-1347
-
-
Chen, M.S.1
White, M.C.2
-
23
-
-
18744372130
-
-
b) M. S. Chen, N. Prabagaran, N. A. Labenz, M. C. White, J. Am. Chem. Soc. 2005, 127, 6970-6971;
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 6970-6971
-
-
Chen, M.S.1
Prabagaran, N.2
Labenz, N.A.3
White, M.C.4
-
24
-
-
33750180621
-
-
c) T. Mitsudome, T. Umetani, N. Nosaka, K. Mori, T. Mizugaki, K. Ebitani, K. Kaneda, Angew. Chem. 2006, 118, 495-499;
-
(2006)
Angew. Chem
, vol.118
, pp. 495-499
-
-
Mitsudome, T.1
Umetani, T.2
Nosaka, N.3
Mori, K.4
Mizugaki, T.5
Ebitani, K.6
Kaneda, K.7
-
25
-
-
30444437460
-
-
Angew. Chem. Int. Ed. 2006, 45, 481-485.
-
(2006)
Angew. Chem. Int. Ed
, vol.45
, pp. 481-485
-
-
-
26
-
-
34250877913
-
-
For an example of Pd-catalyzed oxidative allylic amination of unactivated alkenes this is limited to an intramolecular case and requires quinone as the stoichiometric oxidant, see: a K. J. Fraunhoffer, M. C. White, J. Am. Chem. Soc. 2007, 129, 7274-7276;
-
For an example of Pd-catalyzed oxidative allylic amination of unactivated alkenes this is limited to an intramolecular case and requires quinone as the stoichiometric oxidant, see: a) K. J. Fraunhoffer, M. C. White, J. Am. Chem. Soc. 2007, 129, 7274-7276;
-
-
-
-
27
-
-
0001338814
-
-
For single examples of catalytic allylic C-H amination, see: b
-
For single examples of catalytic allylic C-H amination, see: b) R. C. Larock, T. R. Hightower, L. A. Hasvold, K. P. Peterson, J. Org. Chem. 1996, 61, 3584-3585.
-
(1996)
J. Org. Chem
, vol.61
, pp. 3584-3585
-
-
Larock, R.C.1
Hightower, T.R.2
Hasvold, L.A.3
Peterson, K.P.4
-
28
-
-
41449083866
-
-
A related Pd-catalyzed method for allylic amination of alkenes by using a chromium cocatalyst and benzoquinone as the oxidant appeared just prior to submission of this manuscript; see
-
A related Pd-catalyzed method for allylic amination of alkenes by using a chromium cocatalyst and benzoquinone as the oxidant appeared just prior to submission of this manuscript; see: S. A. Reed, M. C. White, J. Am. Chem. Soc. 2008, 130, 3316-3318.
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 3316-3318
-
-
Reed, S.A.1
White, M.C.2
-
29
-
-
0030968870
-
-
For other metal-catalyzed intermolecular oxidative allylic amination of unactivated olefins, see: a
-
For other metal-catalyzed intermolecular oxidative allylic amination of unactivated olefins, see: a) R. S. Srivastava, K. M. Nicholas, J. Am. Chem. Soc. 1997, 119, 3302-3310;
-
(1997)
J. Am. Chem. Soc
, vol.119
, pp. 3302-3310
-
-
Srivastava, R.S.1
Nicholas, K.M.2
-
30
-
-
0029959361
-
-
b) S. Cenini, F. Ragaini, S. Tollari, D. Paone, J. Am. Chem. Soc. 1996, 118, 11964-11965;
-
(1996)
J. Am. Chem. Soc
, vol.118
, pp. 11964-11965
-
-
Cenini, S.1
Ragaini, F.2
Tollari, S.3
Paone, D.4
-
32
-
-
0001508823
-
-
2 (16.1); see: a) I. Koppel, J. Koppel, F. Degerbeck, L. Grehn, U. Ragnarsson, J. Org. Chem. 1991, 56, 7172-7174;
-
2 (16.1); see: a) I. Koppel, J. Koppel, F. Degerbeck, L. Grehn, U. Ragnarsson, J. Org. Chem. 1991, 56, 7172-7174;
-
-
-
-
34
-
-
53349115492
-
-
D301 (OH) is a basic resin with a structure that is similar to Amberlite IRA93/94. For more information, see
-
D301 (OH) is a basic resin with a structure that is similar to Amberlite IRA93/94. For more information, see http://www.kingresin.com.
-
-
-
-
35
-
-
53349155759
-
-
The nonallylic isomers consist of two major products, the homo-and bishomoallylimide. Other isomers are less than 5%.
-
The nonallylic isomers consist of two major products, the homo-and bishomoallylimide. Other isomers are less than 5%.
-
-
-
-
38
-
-
26944488411
-
-
The role of MA is analogous to that of benzoquinone in other Pd-mediated oxidation reactions that involve nucleophilic attack on π-allylpalladium species. See references [7a and b] and: a J.-E. Bäckvall, S. E. Byström, R. E. Nordberg, J. Org. Chem. 1984, 49, 4619-4631;
-
The role of MA is analogous to that of benzoquinone in other Pd-mediated oxidation reactions that involve nucleophilic attack on π-allylpalladium species. See references [7a and b] and: a) J.-E. Bäckvall, S. E. Byström, R. E. Nordberg, J. Org. Chem. 1984, 49, 4619-4631;
-
-
-
-
40
-
-
33847603525
-
-
c) J.-E. Bäckvall, R. E. Nordberg, E. E. Björkman, C. Moberg, J. Chem. Soc. Chem. Commun. 1980, 943-944;
-
(1980)
J. Chem. Soc. Chem. Commun
, pp. 943-944
-
-
Bäckvall, J.-E.1
Nordberg, R.E.2
Björkman, E.E.3
Moberg, C.4
|