-
1
-
-
0000341815
-
-
For leading reviews, see: a
-
For leading reviews, see: a) D. Lucet, T. L. Gall, C. Mioskowski, Angew. Chem. 1998, 110, 2724;
-
(1998)
Angew. Chem
, vol.110
, pp. 2724
-
-
Lucet, D.1
Gall, T.L.2
Mioskowski, C.3
-
4
-
-
33745110538
-
-
c) S. R. S. S. Kotti, C. Timmons, G. Li, Chem. Biol. Drug Des. 2006, 67, 101.
-
(2006)
Chem. Biol. Drug Des
, vol.67
, pp. 101
-
-
Kotti, S.R.S.S.1
Timmons, C.2
Li, G.3
-
5
-
-
33847087811
-
-
For examples of metal-mediated diamination reactions, see: cobalt-mediated: a P. N. Becker, M. A. White, R. G. Bergman, J. Am. Chem. Soc. 1980, 102, 5676;
-
For examples of metal-mediated diamination reactions, see: cobalt-mediated: a) P. N. Becker, M. A. White, R. G. Bergman, J. Am. Chem. Soc. 1980, 102, 5676;
-
-
-
-
6
-
-
85022465705
-
-
mercury-mediated: b J. Barluenga, L. Alonso-Cires, G. Asensio, Synthesis 1979, 962;
-
mercury-mediated: b) J. Barluenga, L. Alonso-Cires, G. Asensio, Synthesis 1979, 962;
-
-
-
-
7
-
-
0001362632
-
-
manganese-mediated: c W. E. Fristad, T. A. Brandvold, J. R. Peterson, S. R. Thompson, J. Org. Chem. 1985, 50, 3647;
-
manganese-mediated: c) W. E. Fristad, T. A. Brandvold, J. R. Peterson, S. R. Thompson, J. Org. Chem. 1985, 50, 3647;
-
-
-
-
8
-
-
33847090307
-
-
osmium-mediated: d A. O. Chong, K. Oshima, K. B. Sharpless, J. Am. Chem. Soc. 1977, 99, 3420;
-
osmium-mediated: d) A. O. Chong, K. Oshima, K. B. Sharpless, J. Am. Chem. Soc. 1977, 99, 3420;
-
-
-
-
12
-
-
0000748578
-
palladium-mediated: H) J.-E. Bäckvall
-
palladium-mediated: h) J.-E. Bäckvall, Tetrahedron Lett. 1978, 19, 163;
-
(1978)
Tetrahedron Lett
, vol.19
, pp. 163
-
-
-
13
-
-
54249118814
-
-
thallium-mediated: i V. G. Aranda, J. Barluenga, F. Aznar, Synthesis 1974, 504.
-
thallium-mediated: i) V. G. Aranda, J. Barluenga, F. Aznar, Synthesis 1974, 504.
-
-
-
-
14
-
-
23844527400
-
-
For recent copper(II)-mediated intramolecular diamination, see: a) T. P. Zabawa, D. Kasi, S. R. Chemler, J. Am. Chem. Soc. 2005, 127, 11250;
-
For recent copper(II)-mediated intramolecular diamination, see: a) T. P. Zabawa, D. Kasi, S. R. Chemler, J. Am. Chem. Soc. 2005, 127, 11250;
-
-
-
-
16
-
-
54249090892
-
-
2, see: a) G. Li, H.-X. Wei, S. H. Kim, M. D. Carducci, Angew. Chem. 2001, 113, 4407;
-
2, see: a) G. Li, H.-X. Wei, S. H. Kim, M. D. Carducci, Angew. Chem. 2001, 113, 4407;
-
-
-
-
18
-
-
0037067329
-
-
b) H.-X. Wei, S. H. Kim, G. Li, J. Org. Chem. 2002, 67, 4777.
-
(2002)
J. Org. Chem
, vol.67
, pp. 4777
-
-
Wei, H.-X.1
Kim, S.H.2
Li, G.3
-
19
-
-
19744362485
-
-
For a recent example of palladium(II)-catalyzed intermolecular diamination of conjugated dienes, see: G. L. J. Bar, G. C. Lloyd-Jones, K. I. Booker-Milburn, J. Am. Chem. Soc. 2005, 127, 7308.
-
For a recent example of palladium(II)-catalyzed intermolecular diamination of conjugated dienes, see: G. L. J. Bar, G. C. Lloyd-Jones, K. I. Booker-Milburn, J. Am. Chem. Soc. 2005, 127, 7308.
-
-
-
-
20
-
-
27144440348
-
-
For recent examples of palladium(II)- and nickel(II)-catalyzed intramolecular diamination of olefins, see: a) J. Streuff, C. H. Hövelmann, M. Nieger, K. Muñiz, J. Am. Chem. Soc. 2005, 127, 14586;
-
For recent examples of palladium(II)- and nickel(II)-catalyzed intramolecular diamination of olefins, see: a) J. Streuff, C. H. Hövelmann, M. Nieger, K. Muñiz, J. Am. Chem. Soc. 2005, 127, 14586;
-
-
-
-
21
-
-
54249111121
-
-
b) K. Muñiz, J. Streuff, C. H. Hövelmann, A. Núñez, Angew. Chem. 2007, 119, 7255;
-
(2007)
Angew. Chem
, vol.119
, pp. 7255
-
-
Muñiz, K.1
Streuff, J.2
Hövelmann, C.H.3
Núñez, A.4
-
24
-
-
41449087573
-
-
d) K. Muñiz, C. H. Hövelmann, J. Streuff, J. Am. Chem. Soc. 2008, 130, 763;
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 763
-
-
Muñiz, K.1
Hövelmann, C.H.2
Streuff, J.3
-
25
-
-
43749124197
-
-
e) C. H. Hövelmann, J. Streuff, L. Brelot, K. Muñiz, Chem. Commun. 2008, 2334.
-
(2008)
Chem. Commun
, pp. 2334
-
-
Hövelmann, C.H.1
Streuff, J.2
Brelot, L.3
Muñiz, K.4
-
26
-
-
0042401093
-
-
F. D. Greene, J. C. Stowell, W. R. Bergmark, J. Org. Chem. 1969, 34, 2254.
-
(1969)
J. Org. Chem
, vol.34
, pp. 2254
-
-
Greene, F.D.1
Stowell, J.C.2
Bergmark, W.R.3
-
27
-
-
33846624362
-
-
a) H. Du, B. Zhao, Y. Shi, J. Am. Chem. Soc. 2007, 129, 762;
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 762
-
-
Du, H.1
Zhao, B.2
Shi, Y.3
-
28
-
-
34548770013
-
-
b) L. Xu, H. Du, Y. Shi, J. Org. Chem. 2007, 72, 7038;
-
(2007)
J. Org. Chem
, vol.72
, pp. 7038
-
-
Xu, L.1
Du, H.2
Shi, Y.3
-
29
-
-
34748841069
-
-
c) H. Du, W. Yuan, B. Zhao, Y. Shi, J. Am. Chem. Soc. 2007, 129, 11688;
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 11688
-
-
Du, H.1
Yuan, W.2
Zhao, B.3
Shi, Y.4
-
31
-
-
34547198807
-
-
W. Yuan, H. Du, B. Zhao, Y. Shi, Org. Lett. 2007, 9, 2589.
-
(2007)
Org. Lett
, vol.9
, pp. 2589
-
-
Yuan, W.1
Du, H.2
Zhao, B.3
Shi, Y.4
-
32
-
-
34250863844
-
-
a) H. Du, W. Yuan, B. Zhao, Y. Shi, J. Am. Chem. Soc. 2007, 129, 7496;
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 7496
-
-
Du, H.1
Yuan, W.2
Zhao, B.3
Shi, Y.4
-
33
-
-
46949104564
-
-
b) H. Du, B. Zhao, Y. Shi, J. Am. Chem. Soc. 2008, 130, 8590.
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 8590
-
-
Du, H.1
Zhao, B.2
Shi, Y.3
-
34
-
-
0001186123
-
-
For a leading reference on 4, see: J. W. Timberlake, J. Alender, A. W. Garner, M. L. Hodges, C. Özmeral, S. Szilagyi, J. O. Jacobus, J. Org. Chem. 1981, 46, 2082.
-
For a leading reference on 4, see: J. W. Timberlake, J. Alender, A. W. Garner, M. L. Hodges, C. Özmeral, S. Szilagyi, J. O. Jacobus, J. Org. Chem. 1981, 46, 2082.
-
-
-
-
35
-
-
36849045727
-
-
For an example of copper(I)-catalyzed diamination using 4, see: B. Zhao, W. Yuan, H. Du, Y. Shi, Org. Lett. 2007, 9, 4943.
-
For an example of copper(I)-catalyzed diamination using 4, see: B. Zhao, W. Yuan, H. Du, Y. Shi, Org. Lett. 2007, 9, 4943.
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-
-
-
36
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54249138339
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Trace amounts of product resulting from diamination at the terminal carbon centers were formed for diene 6
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Trace amounts of product resulting from diamination at the terminal carbon centers were formed for diene 6.
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-
-
-
37
-
-
0001312564
-
-
2, see: a) B. M. Trost, Acc. Chem. Res. 1980, 13, 385;
-
2, see: a) B. M. Trost, Acc. Chem. Res. 1980, 13, 385;
-
-
-
-
38
-
-
30444431520
-
-
Ed, E.-i. Negishi, Wiley, New York
-
b) B. Åkermark, K. Zetterberg in Handbook of Organopalladium Chemistry for Organic Synthesis (Ed.: E.-i. Negishi), Wiley, New York, 2002, p. 1875.
-
(2002)
Handbook of Organopalladium Chemistry for Organic Synthesis
, pp. 1875
-
-
Åkermark, B.1
Zetterberg, K.2
-
40
-
-
41449083866
-
-
2, see: S. A. Reed, M. C. White, J. Am. Chem. Soc. 2008, 130, 3316.
-
2, see: S. A. Reed, M. C. White, J. Am. Chem. Soc. 2008, 130, 3316.
-
-
-
-
41
-
-
0000518357
-
-
For leading reviews on palladium(II)-catalyzed cyclization of N and O nucleophiles onto olefins, see: a) L. S. Hegedus, Tetrahedron 1984, 40, 2415;
-
For leading reviews on palladium(II)-catalyzed cyclization of N and O nucleophiles onto olefins, see: a) L. S. Hegedus, Tetrahedron 1984, 40, 2415;
-
-
-
-
46
-
-
34047161855
-
-
f) V. Kotov, C. C. Scarborough, S. S. Stahl, Inorg. Chem. 2007, 46, 1910.
-
(2007)
Inorg. Chem
, vol.46
, pp. 1910
-
-
Kotov, V.1
Scarborough, C.C.2
Stahl, S.S.3
-
47
-
-
54249098803
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Internal diamination products from the resulting dienes were also observed
-
Internal diamination products from the resulting dienes were also observed.
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48
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54249170240
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For leading references on the formation of dienes from [(π-allyl) Pd] complexes, see: a) Ref. [14a];
-
For leading references on the formation of dienes from [(π-allyl) Pd] complexes, see: a) Ref. [14a];
-
-
-
-
49
-
-
33749868637
-
-
Ed, E.-i. Negishi, Wiley, New York
-
b) I. Shimizu, in Handbook of Organopalladium Chemistry for Organic Synthesis (Ed.: E.-i. Negishi), Wiley, New York, 2002, p. 1981.
-
(2002)
Handbook of Organopalladium Chemistry for Organic Synthesis
, pp. 1981
-
-
Shimizu, I.1
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