-
1
-
-
0002782655
-
-
For reviews of α-alkylation of carbonyl compounds, see: In;, Eds.; Oxford University Press: New York, Vol., pp.
-
For reviews of α-alkylation of carbonyl compounds, see: Caine, D. In Comprehensive Organic Synthesis; Trost, B. M. and Fleming, I., Eds.; Oxford University Press: New York, 1991; Vol. 9, pp 1-63.
-
(1991)
Comprehensive Organic Synthesis
, vol.9
, pp. 1-63
-
-
Caine, D.1
Trost, B.M.2
Fleming, I.3
-
3
-
-
74849140182
-
-
Johansson, C. C. C.; Colacot, T. J. Angew. Chem., Int. Ed. 2010, 49, 676
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, pp. 676
-
-
Johansson, C.C.C.1
Colacot, T.J.2
-
6
-
-
42049098605
-
-
For a recent account of metal-free arylation, see
-
For a recent account of metal-free arylation, see: Dichiarante, V.; Fagnoni, M. Synlett 2008, 787
-
(2008)
Synlett
, pp. 787
-
-
Dichiarante, V.1
Fagnoni, M.2
-
7
-
-
0001461267
-
-
For selected reviews of organobismuth reagents, see
-
For selected reviews of organobismuth reagents, see: Barton, D. H. R.; Finet, J.-P. Pure Appl. Chem. 1987, 59, 937
-
(1987)
Pure Appl. Chem.
, vol.59
, pp. 937
-
-
Barton, D.H.R.1
Finet, J.-P.2
-
8
-
-
40849085240
-
-
Abramovitch, R. A.; Barton, D. H. R.; Finet, J.-P. Tetrahedron 1988, 44, 3039
-
(1988)
Tetrahedron
, vol.44
, pp. 3039
-
-
Abramovitch, R.A.1
Barton, D.H.R.2
Finet, J.-P.3
-
10
-
-
0035796429
-
-
For recent applications, see:;; J. Am. Chem. Soc. 2003, 125, 10494
-
Elliott, G.; Konopelski, J. P. Tetrahedron 2001, 57, 5683 For recent applications, see: Ooi, T.; Goto, R.; Maruoka, K. J. Am. Chem. Soc. 2003, 125, 10494
-
(2001)
Tetrahedron
, vol.57
, pp. 5683
-
-
Elliott, G.1
Konopelski, J.P.2
Ooi, T.3
Goto, R.4
Maruoka, K.5
-
13
-
-
0028856166
-
-
For selected examples of the use of organolead reagents, see
-
For selected examples of the use of organolead reagents, see: Orito, K.; Sasaki, T.; Suginome, H. J. Org. Chem. 1995, 60, 6208
-
(1995)
J. Org. Chem.
, vol.60
, pp. 6208
-
-
Orito, K.1
Sasaki, T.2
Suginome, H.3
-
14
-
-
33748594965
-
-
Morgan, J.; Pinhey, J. T.; Rowe, B. R. J. Chem. Soc., Perkin Trans. 1 1997, 1005
-
(1997)
J. Chem. Soc., Perkin Trans. 1
, pp. 1005
-
-
Morgan, J.1
Pinhey, J.T.2
Rowe, B.R.3
-
15
-
-
0000349617
-
-
Elliott, G. I.; Konopelski, J. P.; Olmstead, M. M. Org. Lett. 1999, 1, 1867
-
(1999)
Org. Lett.
, vol.1
, pp. 1867
-
-
Elliott, G.I.1
Konopelski, J.P.2
Olmstead, M.M.3
-
17
-
-
34548734673
-
-
Xia, J.; Brown, L. E.; Konopelski, J. P. J. Org. Chem. 2007, 72, 6885
-
(2007)
J. Org. Chem.
, vol.72
, pp. 6885
-
-
Xia, J.1
Brown, L.E.2
Konopelski, J.P.3
-
18
-
-
59049089106
-
-
For recent reviews of polyvalent iodine, see
-
For recent reviews of polyvalent iodine, see: Zhdankin, V. V.; Stang, P. J. Chem. Rev. 2008, 108, 5299
-
(2008)
Chem. Rev.
, vol.108
, pp. 5299
-
-
Zhdankin, V.V.1
Stang, P.J.2
-
19
-
-
70449597257
-
-
3- iodanes as arylation reagents, see:; Tetrahedron 2009, 65, 3149
-
3-iodanes as arylation reagents, see: Eastman, K.; Baran, P. S. Tetrahedron 2009, 65, 3149
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 9052
-
-
Olofsson, B.1
Merritt, E.A.2
Eastman, K.3
Baran, P.S.4
-
20
-
-
77954856046
-
-
Norrby, P.-O.; Petersen, T. B.; Bielawski, M.; Olofsson, B. Chem.-Eur. J. 2010, 16, 8251
-
(2010)
Chem.-Eur. J.
, vol.16
, pp. 8251
-
-
Norrby, P.-O.1
Petersen, T.B.2
Bielawski, M.3
Olofsson, B.4
-
21
-
-
17644362249
-
-
For recent selected examples of the use of arynes as arylation reagents, see
-
For recent selected examples of the use of arynes as arylation reagents, see: Tambar, U. K.; Stoltz, B. M. J. Am. Chem. Soc. 2005, 127, 5340
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 5340
-
-
Tambar, U.K.1
Stoltz, B.M.2
-
23
-
-
68049103230
-
-
Liu, Y.-L.; Liang, Y.; Pi, S.-F.; Li, J.-H. J. Org. Chem. 2009, 74, 5691
-
(2009)
J. Org. Chem.
, vol.74
, pp. 5691
-
-
Liu, Y.-L.1
Liang, Y.2
Pi, S.-F.3
Li, J.-H.4
-
24
-
-
77949851037
-
-
Tadross, P. M.; Gilmore, C. D.; Bugga, P.; Virgil, S. C.; Stoltz, B. M. Org. Lett. 2010, 12, 1224
-
(2010)
Org. Lett.
, vol.12
, pp. 1224
-
-
Tadross, P.M.1
Gilmore, C.D.2
Bugga, P.3
Virgil, S.C.4
Stoltz, B.M.5
-
25
-
-
15744377645
-
-
For nucleophilic aromatic substitution reactions, see
-
For nucleophilic aromatic substitution reactions, see: Bella, M.; Kobbelgaard, S.; Jørgensen, K. A. J. Am. Chem. Soc. 2005, 127, 3670
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 3670
-
-
Bella, M.1
Kobbelgaard, S.2
Jørgensen, K.A.3
-
26
-
-
33745450163
-
-
Kobbelgaard, S.; Bella, M.; Jørgensen, K. A. J. Org. Chem. 2006, 71, 4980
-
(2006)
J. Org. Chem.
, vol.71
, pp. 4980
-
-
Kobbelgaard, S.1
Bella, M.2
Jørgensen, K.A.3
-
27
-
-
77949708742
-
-
Prüger, B.; Hofmeister, G. E.; Jacobsen, C. B.; Alberg, D. G.; Nielsen, M.; Jørgensen, K. A. Chem.-Eur. J. 2010, 16, 3783
-
(2010)
Chem.-Eur. J.
, vol.16
, pp. 3783
-
-
Prüger, B.1
Hofmeister, G.E.2
Jacobsen, C.B.3
Alberg, D.G.4
Nielsen, M.5
Jørgensen, K.A.6
-
28
-
-
34547184381
-
-
Alemán, J.; Richter, B.; Jørgensen, K. A. Angew. Chem., Int. Ed. 2007, 46, 5515
-
(2007)
Angew. Chem., Int. Ed.
, vol.46
, pp. 5515
-
-
Alemán, J.1
Richter, B.2
Jørgensen, K.A.3
-
29
-
-
34547178180
-
-
Alemán, J.; Cabrera, S.; Maerten, E.; Overgaard, J.; Jørgensen, K. A. Angew. Chem., Int. Ed. 2007, 46, 5520
-
(2007)
Angew. Chem., Int. Ed.
, vol.46
, pp. 5520
-
-
Alemán, J.1
Cabrera, S.2
Maerten, E.3
Overgaard, J.4
Jørgensen, K.A.5
-
30
-
-
73349084638
-
-
Jensen, K. L.; Franke, P. T.; Nielsen, L. T.; Daasbjerg, K.; Jørgensen, K. A. Angew. Chem., Int. Ed. 2010, 49, 129
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, pp. 129
-
-
Jensen, K.L.1
Franke, P.T.2
Nielsen, L.T.3
Daasbjerg, K.4
Jørgensen, K.A.5
-
31
-
-
69049104186
-
-
Conrad, J. C.; Kong, J.; Laforteza, B. N.; MacMillan, D. W. C. J. Am. Chem. Soc. 2009, 131, 11640
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 11640
-
-
Conrad, J.C.1
Kong, J.2
Laforteza, B.N.3
MacMillan, D.W.C.4
-
32
-
-
77951688144
-
-
Um, J. M.; Gutierrez, O.; Schoenebeck, F.; Houk, K. N.; MacMillan, D. W. C. J. Am. Chem. Soc. 2010, 132, 6001
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 6001
-
-
Um, J.M.1
Gutierrez, O.2
Schoenebeck, F.3
Houk, K.N.4
MacMillan, D.W.C.5
-
33
-
-
36348935166
-
-
For selected examples, see
-
For selected examples, see: Bogle, K. M.; Hirst, D. J.; Dixon, D. J. Org. Lett. 2007, 9, 4901
-
(2007)
Org. Lett.
, vol.9
, pp. 4901
-
-
Bogle, K.M.1
Hirst, D.J.2
Dixon, D.J.3
-
34
-
-
67749114483
-
-
Nicolaou, K. C.; Reingruber, R.; Sarlah, D.; Bräse, S. J. Am. Chem. Soc. 2009, 131, 2086
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 2086
-
-
Nicolaou, K.C.1
Reingruber, R.2
Sarlah, D.3
Bräse, S.4
-
36
-
-
78449246996
-
-
Huang, X.; Goddard, R.; Maulide, N. Angew. Chem., Int. Ed. 2010, 49, 8979
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, pp. 8979
-
-
Huang, X.1
Goddard, R.2
Maulide, N.3
-
37
-
-
33947292899
-
-
For the seminal studies of Martin, see
-
For the seminal studies of Martin, see: Martin, J. C.; Arhart, R. J. J. Am. Chem. Soc. 1971, 93, 2339
-
(1971)
J. Am. Chem. Soc.
, vol.93
, pp. 2339
-
-
Martin, J.C.1
Arhart, R.J.2
-
38
-
-
0003134818
-
-
Martin, J. C.; Arhart, R. J.; Franz, J. A.; Perozzi, E. F.; Kaplan, L. J. Org. Synth. 1977, 57, 22
-
(1977)
Org. Synth.
, vol.57
, pp. 22
-
-
Martin, J.C.1
Arhart, R.J.2
Franz, J.A.3
Perozzi, E.F.4
Kaplan, L.J.5
-
40
-
-
37049113984
-
-
Daves, D., Jr.; Anderson, W. R., Jr.; Pickering, M. V. J. Chem. Soc., Chem. Commun. 1974, 301
-
(1974)
J. Chem. Soc., Chem. Commun.
, pp. 301
-
-
Daves Jr., D.1
Anderson Jr., W.R.2
Pickering, M.V.3
-
42
-
-
54249141380
-
-
Fürstner, A.; Alcarazo, M.; Radkowski, K.; Lehmann, C. W. Angew. Chem., Int. Ed. 2008, 47, 8302
-
(2008)
Angew. Chem., Int. Ed.
, vol.47
, pp. 8302
-
-
Fürstner, A.1
Alcarazo, M.2
Radkowski, K.3
Lehmann, C.W.4
-
43
-
-
79957986525
-
-
The structure of 6aa was unambiguously confirmed by X-ray crystallographic analysis. See the Supporting Information (SI) for details.
-
The structure of 6aa was unambiguously confirmed by X-ray crystallographic analysis. See the Supporting Information (SI) for details.
-
-
-
-
44
-
-
78650301207
-
-
For gold-catalyzed oxyarylation of alkynes, see
-
For gold-catalyzed oxyarylation of alkynes, see: Li, C.-W.; Pati, K.; Lin, G.-Y.; Abu Sohel, S. M.; Hung, H.-H.; Liu, R.-S. Angew. Chem., Int. Ed. 2010, 49, 9891
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, pp. 9891
-
-
Li, C.-W.1
Pati, K.2
Lin, G.-Y.3
Abu Sohel, S.M.4
Hung, H.-H.5
Liu, R.-S.6
-
45
-
-
70350657122
-
-
Cuenca, A. B.; Montserrat, S.; Hossain, K. M.; Mancha, G.; Lled́s, A.; Medio-Siḿn, M.; Ujaque, G.; Asensio, G. Org. Lett. 2009, 11, 4906
-
(2009)
Org. Lett.
, vol.11
, pp. 4906
-
-
Cuenca, A.B.1
Montserrat, S.2
Hossain, K.M.3
Mancha, G.4
Lled́s, A.5
Medio-Siḿn, M.6
Ujaque, G.7
Asensio, G.8
-
46
-
-
79958009409
-
-
The configuration of the major isomer was determined by nuclear Overhauser effect (NOE) experiments. See the SI for details.
-
The configuration of the major isomer was determined by nuclear Overhauser effect (NOE) experiments. See the SI for details.
-
-
-
-
47
-
-
11944251609
-
-
For selected reviews of the Pummerer reaction, see
-
For selected reviews of the Pummerer reaction, see: Carreño, M. C. Chem. Rev. 1995, 95, 1717
-
(1995)
Chem. Rev.
, vol.95
, pp. 1717
-
-
Carreño, M.C.1
-
51
-
-
77955571128
-
-
Smith, L. H. S.; Coote, S. C.; Sneddon, H. F.; Procter, D. J. Angew. Chem., Int. Ed. 2010, 49, 5832
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, pp. 5832
-
-
Smith, L.H.S.1
Coote, S.C.2
Sneddon, H.F.3
Procter, D.J.4
-
52
-
-
79958012332
-
-
The ratio of 6ad to 7ad was 96/4, as measured by GC. For details of the preparation of an authentic sample of 7ad, see the SI.
-
The ratio of 6ad to 7ad was 96/4, as measured by GC. For details of the preparation of an authentic sample of 7ad, see the SI.
-
-
-
-
53
-
-
0030736240
-
-
The use of sulfoxide 5f bearing a tert -butyl group led to α-(phenylsulfanyl) ketoester 9 in good yield: See:;;, and references therein
-
The use of sulfoxide 5f bearing a tert -butyl group led to α-(phenylsulfanyl) ketoester 9 in good yield: See: Redon, M.; Janousek, Z.; Viehe, H. G. Tetrahedron 1997, 53, 15717 and references therein
-
(1997)
Tetrahedron
, vol.53
, pp. 15717
-
-
Redon, M.1
Janousek, Z.2
Viehe, H.G.3
-
54
-
-
32644481382
-
-
For an extended Pummerer reaction of an indole ring, see
-
For an extended Pummerer reaction of an indole ring, see: Akai, S.; Kawashita, N.; Wada, Y.; Satoh, H.; Alinejad, A. H.; Kakiguchi, K.; Kuriwaki, I.; Kita, Y. Tetrahedron Lett. 2006, 47, 1881
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 1881
-
-
Akai, S.1
Kawashita, N.2
Wada, Y.3
Satoh, H.4
Alinejad, A.H.5
Kakiguchi, K.6
Kuriwaki, I.7
Kita, Y.8
-
55
-
-
0030799835
-
-
Kita, Y.; Takeda, Y.; Matsugi, M.; Iio, K.; Gotanda, K.; Murata, K.; Akai, S. Angew. Chem., Int. Ed. Engl. 1997, 36, 1529
-
(1997)
Angew. Chem., Int. Ed. Engl.
, vol.36
, pp. 1529
-
-
Kita, Y.1
Takeda, Y.2
Matsugi, M.3
Iio, K.4
Gotanda, K.5
Murata, K.6
Akai, S.7
-
56
-
-
0034720947
-
-
Akai, S.; Morita, N.; Lio, K.; Nakumura, Y.; Kita, Y. Org. Lett. 2000, 2, 2279
-
(2000)
Org. Lett.
, vol.2
, pp. 2279
-
-
Akai, S.1
Morita, N.2
Lio, K.3
Nakumura, Y.4
Kita, Y.5
-
58
-
-
7044284674
-
-
Akai, S.; Kawashita, N.; Satoh, H.; Wada, Y.; Kakiguchi, K.; Kuriwaki, I.; Kita, Y. Org. Lett. 2004, 6, 3793
-
(2004)
Org. Lett.
, vol.6
, pp. 3793
-
-
Akai, S.1
Kawashita, N.2
Satoh, H.3
Wada, Y.4
Kakiguchi, K.5
Kuriwaki, I.6
Kita, Y.7
-
60
-
-
23044492191
-
-
Feldman, K. S.; Vidulova, D. B.; Karatjas, A. G. J. Org. Chem. 2005, 70, 6429
-
(2005)
J. Org. Chem.
, vol.70
, pp. 6429
-
-
Feldman, K.S.1
Vidulova, D.B.2
Karatjas, A.G.3
-
63
-
-
79958005155
-
-
Reference 18.
-
Reference 18.
-
-
-
-
64
-
-
66149130268
-
-
For analogous charge-accelerated sulfonium rearrangements in more complex systems, see
-
For analogous charge-accelerated sulfonium rearrangements in more complex systems, see: Yoshida, S.; Yorimitsu, H.; Oshima, K. Org. Lett. 2009, 11, 2185
-
(2009)
Org. Lett.
, vol.11
, pp. 2185
-
-
Yoshida, S.1
Yorimitsu, H.2
Oshima, K.3
-
65
-
-
77953504249
-
-
Kobatake, T.; Yoshida, S.; Yorimitsu, H.; Oshima, K. Angew. Chem., Int. Ed. 2010, 49, 2340
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, pp. 2340
-
-
Kobatake, T.1
Yoshida, S.2
Yorimitsu, H.3
Oshima, K.4
-
66
-
-
77956067595
-
-
Kobatake, T.; Fujino, D.; Yoshida, S.; Yorimitsu, H.; Oshima, K. J. Am. Chem. Soc. 2010, 132, 11838
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 11838
-
-
Kobatake, T.1
Fujino, D.2
Yoshida, S.3
Yorimitsu, H.4
Oshima, K.5
-
67
-
-
38349166185
-
-
Yoshida, S.; Yorimitsu, H.; Oshima, K. Org. Lett. 2007, 9, 5573
-
(2007)
Org. Lett.
, vol.9
, pp. 5573
-
-
Yoshida, S.1
Yorimitsu, H.2
Oshima, K.3
-
68
-
-
49149120184
-
-
Yoshida, S.; Yorimitsu, H.; Oshima, K. Chem. Lett. 2008, 37, 786
-
(2008)
Chem. Lett.
, vol.37
, pp. 786
-
-
Yoshida, S.1
Yorimitsu, H.2
Oshima, K.3
-
69
-
-
77649110096
-
-
For charge-accelerated Claisen rearrangements, see:;;, and references therein.
-
For charge-accelerated Claisen rearrangements, see: Madelaine, C.; Valerio, V.; Maulide, N. Angew. Chem., Int. Ed. 2010, 49, 1583 and references therein.
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, pp. 1583
-
-
Madelaine, C.1
Valerio, V.2
Maulide, N.3
-
70
-
-
0032481391
-
-
For selected applications of sulfonium ylide rearrangements, see
-
For selected applications of sulfonium ylide rearrangements, see: Berger, R.; Ziller, J. W.; Van Vranken, D. L. J. Am. Chem. Soc. 1998, 120, 841
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 841
-
-
Berger, R.1
Ziller, J.W.2
Van Vranken, D.L.3
-
71
-
-
27544467423
-
-
Ma, M.; Peng, L.; Li, C.; Zhang, X.; Wang, J. J. Am. Chem. Soc. 2005, 127, 15016
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 15016
-
-
Ma, M.1
Peng, L.2
Li, C.3
Zhang, X.4
Wang, J.5
-
73
-
-
53549118877
-
-
Boyarskikh, V.; Nyong, A.; Rainier, J. D. Angew. Chem., Int. Ed. 2008, 47, 5374
-
(2008)
Angew. Chem., Int. Ed.
, vol.47
, pp. 5374
-
-
Boyarskikh, V.1
Nyong, A.2
Rainier, J.D.3
-
74
-
-
79958007005
-
-
For examples of alternative synthetically useful manipulations of aromatic sulfanyl substituents (i.e., C-C bond-forming reactions), see refs 18e and 22d.
-
For examples of alternative synthetically useful manipulations of aromatic sulfanyl substituents (i.e., C-C bond-forming reactions), see refs 18e and 22d.
-
-
-
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