-
1
-
-
84891568337
-
-
Ed, J.-E. BGckvall, Wiley-VCH, Weinheim
-
a) Modern Oxidation Methods (Ed.: J.-E. BGckvall), Wiley-VCH, Weinheim, 2004;
-
(2004)
Modern Oxidation Methods
-
-
-
2
-
-
53549100817
-
-
b Comprehensive Organic Synthesis (Eds.: B. M. Trost, I. A. Fleming), Pergamon, Oxford, 1991.
-
b )Comprehensive Organic Synthesis (Eds.: B. M. Trost, I. A. Fleming), Pergamon, Oxford, 1991.
-
-
-
-
3
-
-
36849030278
-
-
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
-
4
-
-
53549101085
-
-
b) S. S. Stahl, Angew. Chem. 2004, 116, 3425-3445;
-
(2004)
Angew. Chem
, vol.116
, pp. 3425-3445
-
-
Stahl, S.S.1
-
5
-
-
4143153074
-
-
Angew. Chem. Int. Ed. 2004, 43, 3400-3420.
-
(2004)
Angew. Chem. Int. Ed
, vol.43
, pp. 3400-3420
-
-
-
6
-
-
33750509858
-
-
IV, see: a J.-Q. Yu, R. Giri, X. Chen, Org. Biomol. Chem. 2006, 4, 4041-4047;
-
IV, see: a) J.-Q. Yu, R. Giri, X. Chen, Org. Biomol. Chem. 2006, 4, 4041-4047;
-
-
-
-
7
-
-
33846503323
-
-
b) O. Daugulis, V. G. Zaitsev, D. Shabashov, O.-N. Pham, A. Lazareva, Synlett 2006, 3382-3388;
-
(2006)
Synlett
, pp. 3382-3388
-
-
Daugulis, O.1
Zaitsev, V.G.2
Shabashov, D.3
Pham, O.-N.4
Lazareva, A.5
-
9
-
-
34047101384
-
-
and references cited therein
-
d) N. R. Deprez, M. S. Sanford, Inorg. Chem. 2007, 46, 1924-1935, and references cited therein.
-
(2007)
Inorg. Chem
, vol.46
, pp. 1924-1935
-
-
Deprez, N.R.1
Sanford, M.S.2
-
10
-
-
19744375923
-
-
a) E. J. Alexanian, C. Lee, E. J. Sorensen, J. Am. Chem. Soc. 2005, 127, 7690-7691;
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 7690-7691
-
-
Alexanian, E.J.1
Lee, C.2
Sorensen, E.J.3
-
13
-
-
34547480362
-
-
Angew. Chem. Int. Ed. 2007, 46, 5737-5740;
-
(2007)
Angew. Chem. Int. Ed
, vol.46
, pp. 5737-5740
-
-
-
14
-
-
41449108079
-
-
d) Y. Li, D. Song, V. M. Dong, J. Am. Chem. Soc. 2008, 130, 2962-2964.
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 2962-2964
-
-
Li, Y.1
Song, D.2
Dong, V.M.3
-
15
-
-
27144440348
-
-
a) J. Streuff, C. H. Hövelmann, M. Nieger, K. Muñiz, J. Am. Chem. Soc. 2005, 127, 14586-14587;
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 14586-14587
-
-
Streuff, J.1
Hövelmann, C.H.2
Nieger, M.3
Muñiz, K.4
-
16
-
-
53549120978
-
-
b) K. Muñiz, J. Am. Chem. Soc. 2007, 129, 14 542-14543;
-
(2007)
J. Am. Chem. Soc
, vol.129
, Issue.14
, pp. 542-14543
-
-
Muñiz, K.1
-
17
-
-
41449087573
-
-
c) K. Muñiz, C. H. Hövelmann, J. Streuff, J. Am. Chem. Soc. 2008, 130, 763-773.
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 763-773
-
-
Muñiz, K.1
Hövelmann, C.H.2
Streuff, J.3
-
18
-
-
34248577469
-
-
a) L. L. Welbes, T. W. Lyons, K. A. Cychosz, M. S. Sanford, J. Am. Chem. Soc. 2007, 129, 5836-5837;
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 5836-5837
-
-
Welbes, L.L.1
Lyons, T.W.2
Cychosz, K.A.3
Sanford, M.S.4
-
19
-
-
34247542965
-
-
b) X. Tong, M. Beller, M. K. Tse, J. Am. Chem. Soc. 2007, 129, 4906-4907.
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 4906-4907
-
-
Tong, X.1
Beller, M.2
Tse, M.K.3
-
21
-
-
0001022539
-
-
For the use of palladium/benzoquinone/hydrogen peroxide as oxidants, see: a
-
For the use of palladium/benzoquinone/hydrogen peroxide as oxidants, see: a) B. Åkermark, E. M. Larsson, J. D. Oslob, J. Org. Chem. 1994, 59, 5729-5733;
-
(1994)
J. Org. Chem
, vol.59
, pp. 5729-5733
-
-
Åkermark, B.1
Larsson, E.M.2
Oslob, J.D.3
-
22
-
-
0000535433
-
-
b) C. Jia, P. MOller, H. Mimoun, J. Mol. Catal. A 1995, 101, 127-136;
-
(1995)
J. Mol. Catal. A
, vol.101
, pp. 127-136
-
-
Jia, C.1
MOller, P.2
Mimoun, H.3
-
23
-
-
0035923308
-
-
c) C. Querci, R. D'Aloisio, R. Bortolo, M. Ricci, D. Bianchi, J. Mol. Catal. A 2001, 176, 95-100.
-
(2001)
J. Mol. Catal. A
, vol.176
, pp. 95-100
-
-
Querci, C.1
D'Aloisio, R.2
Bortolo, R.3
Ricci, M.4
Bianchi, D.5
-
24
-
-
0037028556
-
-
2 disproportionation, see the Supporting Information of: a B. A. Steinhoff, S. R. Fix, S. S. Stahl, J. Am. Chem. Soc. 2002, 124, 766-767;
-
2 disproportionation, see the Supporting Information of: a) B. A. Steinhoff, S. R. Fix, S. S. Stahl, J. Am. Chem. Soc. 2002, 124, 766-767;
-
-
-
-
25
-
-
33644645936
-
-
and b B. A. Steinhoff, A. E. King, S. S. Stahl, J. Org. Chem. 2006, 71, 1861-1868;
-
and b) B. A. Steinhoff, A. E. King, S. S. Stahl, J. Org. Chem. 2006, 71, 1861-1868;
-
-
-
-
27
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53549104501
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IV species proceed with retention of configuration, see Ref. [4c].
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IV species proceed with retention of configuration, see Ref. [4c].
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-
28
-
-
33751385850
-
-
2, see: a S. Ma, X. Lu, J. Org. Chem. 1993, 58, 1245-1250;
-
2, see: a) S. Ma, X. Lu, J. Org. Chem. 1993, 58, 1245-1250;
-
-
-
-
31
-
-
0003995267
-
-
For reviews on chloropalladation, see: a, Ed, E. J. Nigishi, Wiley-VCH, Weinheim
-
For reviews on chloropalladation, see: a) X. Lu, Handbook of Organopalladium Chemistry for Organic Synthesis, V2 (Ed.: E. J. Nigishi), Wiley-VCH, Weinheim, 2002, pp. 2267-2287;
-
(2002)
Handbook of Organopalladium Chemistry for Organic Synthesis, V2
, pp. 2267-2287
-
-
Lu, X.1
-
33
-
-
33244484834
-
-
a) A. M. Johns, M. Utsunomiya, C. D. Incarvito, J. F. Hartwig, J. Am. Chem. Soc. 2006, 128, 1828-1839;
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 1828-1839
-
-
Johns, A.M.1
Utsunomiya, M.2
Incarvito, C.D.3
Hartwig, J.F.4
-
34
-
-
33845582904
-
-
b) A. M. Johns, J. W. Tye, J. F. Hartwig, J. Am. Chem. Soc. 2006, 128, 16010-16011;
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 16010-16011
-
-
Johns, A.M.1
Tye, J.W.2
Hartwig, J.F.3
-
35
-
-
0001462910
-
-
c) J.-E. Bäckvall, J.-E. Nyström, R. E. Nordberg, J. Am. Chem. Soc. 1985, 107, 3676-3686.
-
(1985)
J. Am. Chem. Soc
, vol.107
, pp. 3676-3686
-
-
Bäckvall, J.-E.1
Nyström, J.-E.2
Nordberg, R.E.3
-
36
-
-
0037253324
-
-
Y.-A. Lee, K. H. Yoo, O.-S. Jung, Bull. Chem. Soc. Jpn. 2003, 76, 107-110.
-
(2003)
Bull. Chem. Soc. Jpn
, vol.76
, pp. 107-110
-
-
Lee, Y.-A.1
Yoo, K.H.2
Jung, O.-S.3
-
37
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53549133448
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-; values from R. C. Weast, Handbook of Chemistry and Physics, 50th ed., The Chemical Rubber Co., Cleveland, 1969, D-110;
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-; values from R. C. Weast, Handbook of Chemistry and Physics, 50th ed., The Chemical Rubber Co., Cleveland, 1969, D-110;
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38
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53549107013
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- system, values from http://www.lenntech.com/hydrogen-peroxide.htm.
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- system, values from http://www.lenntech.com/hydrogen-peroxide.htm.
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39
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14544273703
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For recent examples in which Pt complexes were used as models for catalytic Pd intermediates, see: a
-
For recent examples in which Pt complexes were used as models for catalytic Pd intermediates, see: a) A. R. Dick, J. W. Kampf, M. S. Sanford, Organometallics 2005, 24, 482-485;
-
(2005)
Organometallics
, vol.24
, pp. 482-485
-
-
Dick, A.R.1
Kampf, J.W.2
Sanford, M.S.3
-
40
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9144262453
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-
b) A. J. Canty, M. C. Denney, G. van Koten, B. W. Skelton, A. H. White, Organometallics 2004, 23, 5432-5439;
-
(2004)
Organometallics
, vol.23
, pp. 5432-5439
-
-
Canty, A.J.1
Denney, M.C.2
van Koten, G.3
Skelton, B.W.4
White, A.H.5
-
41
-
-
3142681619
-
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c) A. J. Canty, J. Patel, T. Rodemann, J. H. Ryan, B. W. Skelton, A. H. White, Organometallics 2004, 23, 3466-3473.
-
(2004)
Organometallics
, vol.23
, pp. 3466-3473
-
-
Canty, A.J.1
Patel, J.2
Rodemann, T.3
Ryan, J.H.4
Skelton, B.W.5
White, A.H.6
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43
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33845551477
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The retention of the configuration at the carbon center during cleavage of the C-Pd bond was observed when CuCl2 was used as the oxidant, see Refs, 11b] and [11c, However, the oxidative cleavage of the C-Pd bond by CuCl2 to form a C-Cl bond with configuration inversion was also reported, see: J.-E. Bäckvall, Acc. Chem. Res. 1983, 16, 335-342
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2 to form a C-Cl bond with configuration inversion was also reported, see: J.-E. Bäckvall, Acc. Chem. Res. 1983, 16, 335-342.
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