-
1
-
-
78651483272
-
-
For reviews on traditional cross-coupling reactions, see
-
For reviews on traditional cross-coupling reactions, see
-
-
-
-
3
-
-
0036589259
-
-
Hassan, J.; Sévignon, M.; Gozzi, C.; Schulz, E.; Lemaire, M. Chem. Rev. 2002, 102, 1359
-
(2002)
Chem. Rev.
, vol.102
, pp. 1359
-
-
Hassan, J.1
Sévignon, M.2
Gozzi, C.3
Schulz, E.4
Lemaire, M.5
-
4
-
-
78651492445
-
-
For selected recent reviews on direct arylation, see
-
For selected recent reviews on direct arylation, see
-
-
-
-
8
-
-
70350494926
-
-
Giri, R.; Shi, B.-F.; Engle, K. M.; Maugel, N.; Yu, J.-Q. Chem. Soc. Rev. 2009, 38, 3242
-
(2009)
Chem. Soc. Rev.
, vol.38
, pp. 3242
-
-
Giri, R.1
Shi, B.-F.2
Engle, K.M.3
Maugel, N.4
Yu, J.-Q.5
-
9
-
-
72449170089
-
-
Ackermann, L.; Vicente, R.; Kapdi, A. R. Angew. Chem., Int. Ed. 2009, 48, 9792
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 9792
-
-
Ackermann, L.1
Vicente, R.2
Kapdi, A.R.3
-
10
-
-
57549092674
-
-
Catellani, M.; Motti, E.; Della Ca, N. Acc. Chem. Res. 2008, 41, 1512
-
(2008)
Acc. Chem. Res.
, vol.41
, pp. 1512
-
-
Catellani, M.1
Motti, E.2
Della Ca, N.3
-
11
-
-
33846918696
-
-
Alberico, D.; Scott, M. E.; Lautens, M. Chem. Rev. 2007, 107, 174
-
(2007)
Chem. Rev.
, vol.107
, pp. 174
-
-
Alberico, D.1
Scott, M.E.2
Lautens, M.3
-
12
-
-
34248361209
-
-
Campeau, L.-C.; Stuart, D. R.; Fagnou, K. Aldrichimica Acta 2007, 40, 35
-
(2007)
Aldrichimica Acta
, vol.40
, pp. 35
-
-
Campeau, L.-C.1
Stuart, D.R.2
Fagnou, K.3
-
15
-
-
70349900402
-
-
For a discussion, see:;, For examples of direct arylation with alkyl palladium(II) intermediates capable of β-hydride elimination see:; J. Org. Chem. 1994, 59, 33
-
For a discussion, see: René, O.; Lapointe, D.; Fagnou, K. Org. Lett. 2009, 11, 4560 For examples of direct arylation with alkyl palladium(II) intermediates capable of β-hydride elimination see: Song, Z. Z.; Wong, H. N. C. J. Org. Chem. 1994, 59, 33
-
(2009)
Org. Lett.
, vol.11
, pp. 4560
-
-
René, O.1
Lapointe, D.2
Fagnou, K.3
Song, Z.Z.4
Wong, H.N.C.5
-
16
-
-
70349934303
-
-
Hu, Y.; Yu, C.; Ren, D.; Hu, Q.; Zhang, L.; Cheng, D. Angew. Chem., Int. Ed. 2009, 48, 5448
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 5448
-
-
Hu, Y.1
Yu, C.2
Ren, D.3
Hu, Q.4
Zhang, L.5
Cheng, D.6
-
17
-
-
33847085137
-
-
Ozawa, F.; Ito, T.; Yamamoto, A. J. Am. Chem. Soc. 1980, 102, 6457
-
(1980)
J. Am. Chem. Soc.
, vol.102
, pp. 6457
-
-
Ozawa, F.1
Ito, T.2
Yamamoto, A.3
-
19
-
-
78651516346
-
-
For examples of direct arylation using alkylpalladium intermediates generated from cyclobutanol fragmentation, see
-
For examples of direct arylation using alkylpalladium intermediates generated from cyclobutanol fragmentation, see
-
-
-
-
20
-
-
0033599513
-
-
Nishimura, T.; Ohe, K.; Uemura, S. J. Am. Chem. Soc. 1999, 121, 2645
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 2645
-
-
Nishimura, T.1
Ohe, K.2
Uemura, S.3
-
21
-
-
0035936747
-
-
For the analogous reaction using cyclobutanone oximes, see:; J. Am. Chem. Soc. 2000, 122, 12049
-
Nishimura, T.; Ohe, K.; Uemura, S. J. Org. Chem. 2001, 66, 1455 For the analogous reaction using cyclobutanone oximes, see: Nishimura, T.; Uemura, S. J. Am. Chem. Soc. 2000, 122, 12049
-
(2001)
J. Org. Chem.
, vol.66
, pp. 1455
-
-
Nishimura, T.1
Ohe, K.2
Uemura, S.3
Nishimura, T.4
Uemura, S.5
-
22
-
-
29844440702
-
-
Buchanan, G. O.; Williams, P. G.; Feling, R. H.; Kauffman, C. A.; Jensen, P. R.; Fenical, W. Org. Lett. 2005, 7, 2731
-
(2005)
Org. Lett.
, vol.7
, pp. 2731
-
-
Buchanan, G.O.1
Williams, P.G.2
Feling, R.H.3
Kauffman, C.A.4
Jensen, P.R.5
Fenical, W.6
-
23
-
-
78651473656
-
-
Cascade Heck reaction
-
Cascade Heck reaction
-
-
-
-
24
-
-
33746464516
-
-
3)-H activation:; Chem.-Eur. J. 2007, 13, 792
-
3)-H activation: Hitce, J.; Retailleau, P.; Baudoin, O. Chem.-Eur. J. 2007, 13, 792
-
(1988)
J. Am. Chem. Soc.
, vol.110
, pp. 2328
-
-
Abelman, M.M.1
Overman, L.E.2
Copéret, C.3
Ma, S.4
Negishi, E.5
Corkey, B.K.6
Toste, F.D.7
Ethirajan, M.8
Oh, H.-S.9
Cha, J.K.10
Hitce, J.11
Retailleau, P.12
Baudoin, O.13
-
25
-
-
77955393861
-
-
Rousseaux, S.; Davi, M.; Sofack-Kreutzer, J.; Pierre, C.; Kefalidis, C. E.; Clot, E.; Fagnou, K.; Baudoin, O. J. Am. Chem. Soc. 2010, 132, 10706
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 10706
-
-
Rousseaux, S.1
Davi, M.2
Sofack-Kreutzer, J.3
Pierre, C.4
Kefalidis, C.E.5
Clot, E.6
Fagnou, K.7
Baudoin, O.8
-
26
-
-
0037771626
-
-
Toyota, M.; Ilangovan, A.; Okamoto, R.; Masaki, T.; Arakawa, M.; Ihara, M. Org. Lett. 2002, 4, 4293
-
(2002)
Org. Lett.
, vol.4
, pp. 4293
-
-
Toyota, M.1
Ilangovan, A.2
Okamoto, R.3
Masaki, T.4
Arakawa, M.5
Ihara, M.6
-
27
-
-
35548943629
-
-
Cruz, A. C. F.; Miller, N. D.; Willis, M. C. Org. Lett. 2007, 9, 4391
-
(2007)
Org. Lett.
, vol.9
, pp. 4391
-
-
Cruz, A.C.F.1
Miller, N.D.2
Willis, M.C.3
-
28
-
-
78651513461
-
-
For a good entry into the metal homoenolate literature, see
-
For a good entry into the metal homoenolate literature, see
-
-
-
-
29
-
-
64549099855
-
-
3)-H activation and subsequent cross-coupling, see:; J. Am. Chem. Soc. 2007, 129, 3510
-
3)-H activation and subsequent cross-coupling, see: Giri, R.; Maugel, N.; Li, J.-J.; Wang, D.-H.; Breazzano, S. P.; Saunders, L. B.; Yu, J.-Q. J. Am. Chem. Soc. 2007, 129, 3510
-
(2009)
J. Org. Chem.
, vol.74
, pp. 1297
-
-
Molander, G.A.1
Jean-Gérard, L.2
Giri, R.3
Maugel, N.4
Li, J.-J.5
Wang, D.-H.6
Breazzano, S.P.7
Saunders, L.B.8
Yu, J.-Q.9
-
30
-
-
44949242600
-
-
Wang, D.-H.; Wasa, M.; Giri, R.; Yu, J.-Q. J. Am. Chem. Soc. 2008, 130, 7190
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 7190
-
-
Wang, D.-H.1
Wasa, M.2
Giri, R.3
Yu, J.-Q.4
-
31
-
-
67651233294
-
-
For a recent example of formal homoenolate arylation, see:; Angew. Chem., Int. Ed. 2010, 49, 7261
-
Wasa, M.; Engle, K. M.; Yu, J.-Q. J. Am. Chem. Soc. 2009, 131, 9886 For a recent example of formal homoenolate arylation, see: Renaudat, A.; Ludivine, J.-G.; Jazzar, R.; Kefalidis, C. E.; Clot, E.; Baudoin, O. Angew. Chem., Int. Ed. 2010, 49, 7261
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 9886
-
-
Wasa, M.1
Engle, K.M.2
Yu, J.-Q.3
Renaudat, A.4
Ludivine, J.-G.5
Jazzar, R.6
Kefalidis, C.E.7
Clot, E.8
Baudoin, O.9
-
33
-
-
78651517176
-
-
This type of coordination of alkenylcyclobutanols has been invoked before; see
-
This type of coordination of alkenylcyclobutanols has been invoked before; see
-
-
-
-
34
-
-
0000370802
-
-
Nemoto, H.; Miyata, J.; Yoshida, M.; Raku, N.; Fukumoto, K. J. Org. Chem. 1997, 62, 7850
-
(1997)
J. Org. Chem.
, vol.62
, pp. 7850
-
-
Nemoto, H.1
Miyata, J.2
Yoshida, M.3
Raku, N.4
Fukumoto, K.5
-
35
-
-
0033613808
-
-
Nemoto, H.; Yoshida, M.; Fukumoto, K.; Ihara, M. Tetrahedron Lett. 1999, 40, 907
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 907
-
-
Nemoto, H.1
Yoshida, M.2
Fukumoto, K.3
Ihara, M.4
-
36
-
-
0034699224
-
-
Yoshida, M.; Ismail, M. A.-H.; Nemoto, H.; Ihara, M. J. Chem. Soc., Perkin Trans. 1 2000, 2629
-
(2000)
J. Chem. Soc., Perkin Trans. 1
, pp. 2629
-
-
Yoshida, M.1
Ismail, M.A.-H.2
Nemoto, H.3
Ihara, M.4
-
37
-
-
78651511145
-
-
See Supporting Information for details
-
See Supporting Information for details.
-
-
-
-
38
-
-
33845534717
-
-
Wang, B.; Shen, Y.-M.; Shi, Y. J. Org. Chem. 2006, 71, 9519
-
(2006)
J. Org. Chem.
, vol.71
, pp. 9519
-
-
Wang, B.1
Shen, Y.-M.2
Shi, Y.3
-
39
-
-
78651485696
-
-
For an early example of palladium-catalyzed β-carboelimination of alkenyl-tert -cyclobutanols under oxidative conditions, see ref 5b. For a related rhodium-catalyzed C-C activation of allenyl-tert -cyclobutanols, see
-
For an early example of palladium-catalyzed β-carboelimination of alkenyl-tert -cyclobutanols under oxidative conditions, see ref 5b. For a related rhodium-catalyzed C-C activation of allenyl-tert -cyclobutanols, see
-
-
-
-
40
-
-
56449094610
-
-
Seiser, T.; Cramer, N. Angew. Chem., Int. Ed. 2008, 47, 9294
-
(2008)
Angew. Chem., Int. Ed.
, vol.47
, pp. 9294
-
-
Seiser, T.1
Cramer, N.2
-
41
-
-
10044267678
-
-
Zhang, H.; Ferreira, E. M.; Stoltz, B. M. Angew. Chem., Int. Ed. 2004, 43, 6144
-
(2004)
Angew. Chem., Int. Ed.
, vol.43
, pp. 6144
-
-
Zhang, H.1
Ferreira, E.M.2
Stoltz, B.M.3
|