-
6
-
-
0032481653
-
-
J. Åhman, J. P. Wolfe, M. V. Troutman, M. Palucki, S. L. Buchwald, J. Am. Chem. Soc. 1998, 120, 1918
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 1918
-
-
Åhman, J.1
Wolfe, J.P.2
Troutman, M.V.3
Palucki, M.4
Buchwald, S.L.5
-
7
-
-
0037138675
-
-
T. Hamada, A. Chieffi, J. Åhman, S. L. Buchwald, J. Am. Chem. Soc. 2002, 124, 1261
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 1261
-
-
Hamada, T.1
Chieffi, A.2
Åhman, J.3
Buchwald, S.L.4
-
8
-
-
33645023302
-
-
G. Chen, F. Y. Kwong, H. O. Chan, W.-Y. Yu, A. S. C. Chan, Chem. Commun. 2006, 1413
-
(2006)
Chem. Commun.
, pp. 1413
-
-
Chen, G.1
Kwong, F.Y.2
Chan, H.O.3
Yu, W.-Y.4
Chan, A.S.C.5
-
10
-
-
38349078282
-
-
X. Liao, Z. Weng, J. F. Hartwig, J. Am. Chem. Soc. 2008, 130, 195.
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 195
-
-
Liao, X.1
Weng, Z.2
Hartwig, J.F.3
-
13
-
-
84866932111
-
-
P. Nareddy, L. Mantilli, L. Guénée, C. Mazet, Angew. Chem. 2012, 124, 3892
-
(2012)
Angew. Chem.
, vol.124
, pp. 3892
-
-
Nareddy, P.1
Mantilli, L.2
Guénée, L.3
Mazet, C.4
-
15
-
-
67651210439
-
-
A. M. Taylor, R. A. Altman, S. L. Buchwald, J. Am. Chem. Soc. 2009, 131, 9900
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 9900
-
-
Taylor, A.M.1
Altman, R.A.2
Buchwald, S.L.3
-
17
-
-
33845579450
-
-
X. Xie, Y. Chen, D. Ma, J. Am. Chem. Soc. 2006, 128, 16050.
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 16050
-
-
Xie, X.1
Chen, Y.2
Ma, D.3
-
18
-
-
84655162040
-
-
A recent review.
-
A recent review:, J. Zhou, Synlett 2012, 1.
-
(2012)
Synlett
, pp. 1
-
-
Zhou, J.1
-
20
-
-
80052330954
-
-
J. S. Harvey, S. P. Simonovich, C. R. Jamison, D. W. C. MacMillan, J. Am. Chem. Soc. 2011, 133, 13782
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 13782
-
-
Harvey, J.S.1
Simonovich, S.P.2
Jamison, C.R.3
MacMillan, D.W.C.4
-
21
-
-
80052328305
-
-
A. Bigot, A. E. Williamson, M. J. Gaunt, J. Am. Chem. Soc. 2011, 133, 13778.
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 13778
-
-
Bigot, A.1
Williamson, A.E.2
Gaunt, M.J.3
-
22
-
-
80053492633
-
-
Z. Huang, Z. Liu, J. Zhou, J. Am. Chem. Soc. 2011, 133, 15882.
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 15882
-
-
Huang, Z.1
Liu, Z.2
Zhou, J.3
-
24
-
-
68549140974
-
-
P. M. Lundin, J. Esquivias, G. C. Fu, Angew. Chem. 2009, 121, 160
-
(2009)
Angew. Chem.
, vol.121
, pp. 160
-
-
Lundin, P.M.1
Esquivias, J.2
Fu, G.C.3
-
26
-
-
0000545221
-
-
M. Kosugi, I. Hagiwara, T. Sumiya, T. Migita, Bull. Chem. Soc. Jpn. 1984, 57, 242.
-
(1984)
Bull. Chem. Soc. Jpn.
, vol.57
, pp. 242
-
-
Kosugi, M.1
Hagiwara, I.2
Sumiya, T.3
Migita, T.4
-
27
-
-
79952600795
-
-
N. Jalalian, E. E. Ishikawa, L. F. Silva, B. Olofsson, Org. Lett. 2011, 13, 1552.
-
(2011)
Org. Lett.
, vol.13
, pp. 1552
-
-
Jalalian, N.1
Ishikawa, E.E.2
Silva, L.F.3
Olofsson, B.4
-
28
-
-
79955413969
-
-
V. L. Rendina, D. C. Moebius, J. S. Kingsbury, Org. Lett. 2011, 13, 2004
-
(2011)
Org. Lett.
, vol.13
, pp. 2004
-
-
Rendina, V.L.1
Moebius, D.C.2
Kingsbury, J.S.3
-
29
-
-
58249112654
-
-
Y.-M. Shen, B. Wang, Y. Shi, Angew. Chem. 2006, 118, 1457
-
(2006)
Angew. Chem.
, vol.118
, pp. 1457
-
-
Shen, Y.-M.1
Wang, B.2
Shi, Y.3
-
31
-
-
0030087784
-
-
G. Delle Monache, B. Botta, V. Vinciguerra, J. F. de Mello, A. de Andrade Chiappeta, Phytochemistry 1996, 41, 537
-
(1996)
Phytochemistry
, vol.41
, pp. 537
-
-
Delle Monache, G.1
Botta, B.2
Vinciguerra, V.3
De Mello, J.F.4
De Andrade Chiappeta, A.5
-
32
-
-
74049162896
-
-
K. Umehara, K. Nemoto, A. Matsushita, E. Terada, O. Monthakantirat, W. De-Eknamkul, T. Miyase, T. Warashina, M. Degawa, H. Noguchi, J. Nat. Prod. 2009, 72, 2163.
-
(2009)
J. Nat. Prod.
, vol.72
, pp. 2163
-
-
Umehara, K.1
Nemoto, K.2
Matsushita, A.3
Terada, E.4
Monthakantirat, O.5
De-Eknamkul, W.6
Miyase, T.7
Warashina, T.8
Degawa, M.9
Noguchi, H.10
-
33
-
-
33845470059
-
-
D. Kruger, A. E. Sopchik, C. A. Kingsbury, J. Org. Chem. 1984, 49, 778.
-
(1984)
J. Org. Chem.
, vol.49
, pp. 778
-
-
Kruger, D.1
Sopchik, A.E.2
Kingsbury, C.A.3
-
34
-
-
49549169170
-
-
A. K. Bose, M. Tsai, S. D. Sharma, M. S. Manhas, Tetrahedron Lett. 1973, 14, 3851.
-
(1973)
Tetrahedron Lett.
, vol.14
, pp. 3851
-
-
Bose, A.K.1
Tsai, M.2
Sharma, S.D.3
Manhas, M.S.4
-
36
-
-
0026686518
-
-
I. Ojima, I. Habus, M. Zhao, M. Zucco, Y. H. Park, C. M. Sun, T. Brigaud, Tetrahedron 1992, 48, 6985.
-
(1992)
Tetrahedron
, vol.48
, pp. 6985
-
-
Ojima, I.1
Habus, I.2
Zhao, M.3
Zucco, M.4
Park, Y.H.5
Sun, C.M.6
Brigaud, T.7
-
38
-
-
84876544410
-
-
WO 2003/006452
-
T. Koskelainen, L. Otsomaa, A. Karjalainen, P. Kotovuori, J. Tenhunen, S. Rasku, P. Nore, E. Tiainen, O. Tormakangas, WO 2003/006452, 2003.
-
(2003)
-
-
Koskelainen, T.1
Otsomaa, L.2
Karjalainen, A.3
Kotovuori, P.4
Tenhunen, J.5
Rasku, S.6
Nore, P.7
Tiainen, E.8
Tormakangas, O.9
-
39
-
-
84876523895
-
-
CCDC 878815 and 878816 contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
-
-
-
-
40
-
-
81755182712
-
-
A previous study reported asymmetric arylation of silyl ester enolates using a Pd/Josiphos catalyst. The O-enolate complex was assumed to form directly from transmetalation to [(L)Pd(Ar)(OAc)] and can undergo direct C-C reductive elimination to form products, but no computational details were given.
-
A previous study reported asymmetric arylation of silyl ester enolates using a Pd/Josiphos catalyst. The O-enolate complex was assumed to form directly from transmetalation to [(L)Pd(Ar)(OAc)] and can undergo direct C-C reductive elimination to form products, but no computational details were given:, K. Kobayashi, Y. Yamamoto, N. Miyaura, Organometallics 2011, 30, 6323.
-
(2011)
Organometallics
, vol.30
, pp. 6323
-
-
Kobayashi, K.1
Yamamoto, Y.2
Miyaura, N.3
-
42
-
-
33644554472
-
-
R. L. Robiette, J. Richardson, V. K. Aggarwal, J. N. Harvey, J. Am. Chem. Soc. 2006, 128, 2394.
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 2394
-
-
Robiette, R.L.1
Richardson, J.2
Aggarwal, V.K.3
Harvey, J.N.4
-
43
-
-
34547185222
-
-
Arylation of an enantioenriched Li enolate of cyclohexanone by diaryl iodonium salts
-
Arylation of an enantioenriched Li enolate of cyclohexanone by diaryl iodonium salts:, V. K. Aggarwal, B. Olofsson, Angew. Chem. 2005, 117, 5652
-
(2005)
Angew. Chem.
, vol.117
, pp. 5652
-
-
Aggarwal, V.K.1
Olofsson, B.2
-
44
-
-
24644484333
-
-
Catalytic asymmetric protonation of silyl enolate of cyclic ketones is generally less efficient than asymmetric coupling for synthesis of enantioenriched α-arylketones
-
Angew. Chem. Int. Ed. 2005, 44, 5516; Catalytic asymmetric protonation of silyl enolate of cyclic ketones is generally less efficient than asymmetric coupling for synthesis of enantioenriched α-arylketones
-
(2005)
Angew. Chem. Int. Ed.
, vol.44
, pp. 5516
-
-
-
45
-
-
34848848323
-
-
A. Yanagisawa, T. Touge, T. Arai, Angew. Chem. 2005, 117, 1570
-
(2005)
Angew. Chem.
, vol.117
, pp. 1570
-
-
Yanagisawa, A.1
Touge, T.2
Arai, T.3
-
48
-
-
69249201073
-
-
Recent review
-
Recent review:, J. T. Mohr, A. Y. Hong, B. M. Stoltz, Nat. Chem. 2009, 1, 359
-
(2009)
Nat. Chem.
, vol.1
, pp. 359
-
-
Mohr, J.T.1
Hong, A.Y.2
Stoltz, B.M.3
-
49
-
-
80051688161
-
-
E. M. Beck, A. M. Hyde, E. N. Jacobsen, Org. Lett. 2011, 13, 4260
-
(2011)
Org. Lett.
, vol.13
, pp. 4260
-
-
Beck, E.M.1
Hyde, A.M.2
Jacobsen, E.N.3
-
50
-
-
80052083175
-
-
C. H. Cheon, O. Kanno, F. D. Toste, J. Am. Chem. Soc. 2011, 133, 13248.
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 13248
-
-
Cheon, C.H.1
Kanno, O.2
Toste, F.D.3
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