-
1
-
-
48749090995
-
-
R. Palchaudhuri, V. Nesterenko, P. J. Hergenrother, J. Am. Chem. Soc. 2008, 130, 10274.
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 10274
-
-
Palchaudhuri, R.1
Nesterenko, V.2
Hergenrother, P.J.3
-
2
-
-
0028263518
-
-
J. D. Elliott, M. A. Lago, R. D. Cousins, A. Gao, J. D. Leber, K. F. Erhard, P. Nambi, N. A. Elshourbagy, C. Kumar, J. Med. Chem. 1994, 37, 1553.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 1553
-
-
Elliott, J.D.1
Lago, M.A.2
Cousins, R.D.3
Gao, A.4
Leber, J.D.5
Erhard, K.F.6
Nambi, P.7
Elshourbagy, N.A.8
Kumar, C.9
-
3
-
-
0028093424
-
-
E. H. Ohlstein, P. Nambi, S. A. Douglas, R. M. Edwards, M. Gellai, A. Lago, J. D. Leber, R. D. Cousins, A. M. Gao, J. S. Frazee, C. E. Peishoff, J. W. Bean, D. S. Eggleston, N. A. Elshourbagy, C. Kumar, J. A. Lee, T. L. Yue, C. Louden, D. P. Brooks, J. Weinstock, G. Feuerstein, G. Poste, R. R. Ruffolo, J. G. Gleason, J. D. Elliott, Proc. Natl. Acad. Sci. USA 1994, 97, 8052.
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 8052
-
-
Ohlstein, E.H.1
Nambi, P.2
Douglas, S.A.3
Edwards, R.M.4
Gellai, M.5
Lago, A.6
Leber, J.D.7
Cousins, R.D.8
Gao, A.M.9
Frazee, J.S.10
Peishoff, C.E.11
Bean, J.W.12
Eggleston, D.S.13
Elshourbagy, N.A.14
Kumar, C.15
Lee, J.A.16
Yue, T.L.17
Louden, C.18
Brooks, D.P.19
Weinstock, J.20
Feuerstein, G.21
Poste, G.22
Ruffolo, R.R.23
Gleason, J.G.24
Elliott, J.D.25
more..
-
4
-
-
0028555488
-
-
R. Muthyala, A. R. Katritzky, X. Lan, Dyes Pigm. 1994, 25, 303.
-
(1994)
Dyes Pigm.
, vol.25
, pp. 303
-
-
Muthyala, R.1
Katritzky, A.R.2
Lan, X.3
-
5
-
-
1542796982
-
-
A. R. Katritzky, V. Gupta, C. Garot, C. V. Stevens, M. F. Gordeev, Heterocycles 1994, 38, 345.
-
(1994)
Heterocycles
, vol.38
, pp. 345
-
-
Katritzky, A.R.1
Gupta, V.2
Garot, C.3
Stevens, C.V.4
Gordeev, M.F.5
-
8
-
-
33744916295
-
-
V. Nair, S. Thomas, S. C. Mathew, K. G. Abhilash, Tetrahedron 2006, 62, 6731.
-
(2006)
Tetrahedron
, vol.62
, pp. 6731
-
-
Nair, V.1
Thomas, S.2
Mathew, S.C.3
Abhilash, K.G.4
-
11
-
-
0242607159
-
-
J. S. Yadav, B. V. S. Reddy, S. Sunitha, Adv. Synth. Catal. 2003, 345, 349.
-
(2003)
Adv. Synth. Catal.
, vol.345
, pp. 349
-
-
Yadav, J.S.1
Reddy, B.V.S.2
Sunitha, S.3
-
12
-
-
0242573177
-
-
C. Ramesh, J. Barerjee, R. Pal, B. Das, Adv. Synth. Catal. 2003, 345, 557.
-
(2003)
Adv. Synth. Catal.
, vol.345
, pp. 557
-
-
Ramesh, C.1
Barerjee, J.2
Pal, R.3
Das, B.4
-
13
-
-
30144444897
-
-
V. Nair, K. G. Abhilash, N. Vidya, Org. Lett. 2005, 7, 5857.
-
(2005)
Org. Lett.
, vol.7
, pp. 5857
-
-
Nair, V.1
Abhilash, K.G.2
Vidya, N.3
-
14
-
-
0001238582
-
-
For a complementary procedure involving vicarious nucleophilic substitution of nitroarenes see: A. R. Katritzky, D. Toader, J. Org. Chem. 1997, 62, 4137.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 4137
-
-
Katritzky, A.R.1
Toader, D.2
-
15
-
-
0006021776
-
-
A. R. Katritzky, X. Lan, J. N. Lam, Chem. Ber. 1991, 124, 1809.
-
(1991)
Chem. Ber.
, vol.124
, pp. 1809
-
-
Katritzky, A.R.1
Lan, X.2
Lam, J.N.3
-
16
-
-
70349958049
-
-
Y.-Z. Li, B.-J. Li, X.-Y. Lu, S. Lin, Z.J. Shi, Angew. Chem. 2009, 121, 3875
-
(2009)
Angew. Chem.
, vol.121
, pp. 3875
-
-
Li, Y.-Z.1
Li, B.-J.2
Lu, X.-Y.3
Lin, S.4
Shi, Z.J.5
-
18
-
-
34250863553
-
-
J. Esquivias, R. G. Arrayas, J. C Carretero, Angew. Chem. 2006, 118, 645
-
(2006)
Angew. Chem.
, vol.118
, pp. 645
-
-
Esquivias, J.1
Arrayas, R.G.2
Carretero, J.C.3
-
21
-
-
38349128181
-
-
B. Liégault, J.-L. Renaud, C. Bruneau, Chem. Soc. Rev. 2008, 37, 290.
-
(2008)
Chem. Soc. Rev.
, vol.37
, pp. 290
-
-
Liégault, B.1
Renaud, J.-L.2
Bruneau, C.3
-
22
-
-
67749113467
-
-
D. Imao, B. W. Glasspoole, V. S. Laberge, C. M. Crudden, J. Am. Chem. Soc. 2009, 131, 5024.
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 5024
-
-
Imao, D.1
Glasspoole, B.W.2
Laberge, V.S.3
Crudden, C.M.4
-
23
-
-
34247624723
-
-
Ed.: L. E. Overman, Wiley, New York
-
M. Uemura in Organic Reactions, Vol. 67 (Ed.: L. E. Overman), Wiley, New York, 2006, p. 217.
-
(2006)
Organic Reactions
, vol.67
, pp. 217
-
-
Uemura, M.1
-
24
-
-
0033594343
-
-
C. A. Merlic, J. C. Walsh, D. J. Tantillo, K. N. Houk, J. Am. Chem. Soc. 1999, 121, 3596.
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 3596
-
-
Merlic, C.A.1
Walsh, J.C.2
Tantillo, D.J.3
Houk, K.N.4
-
25
-
-
0033008670
-
-
A. Pfletschinger, T. K. Dargel, J. W. Bats, H.-G. Schmalz, W. Koch, Chem. Eur. J. 1999, 5, 537.
-
(1999)
Chem. Eur. J.
, vol.5
, pp. 537
-
-
Pfletschinger, A.1
Dargel, T.K.2
Bats, J.W.3
Schmalz, H.-G.4
Koch, W.5
-
27
-
-
17044450134
-
-
V. N. Kalinin, I. A. Cherepanov, S. K. Moiseev, J. Organomet. Chem. 1997, 536-537, 437.
-
(1997)
J. Organomet. Chem.
, vol.536-537
, pp. 437
-
-
Kalinin, V.N.1
Cherepanov, I.A.2
Moiseev, S.K.3
-
28
-
-
34548522962
-
-
A. R. E. Brewer, A. F. Drake, S. E. Gibson, J. T. Rendell, Org. Lett. 2007, 9, 3487.
-
(2007)
Org. Lett.
, vol.9
, pp. 3487
-
-
Brewer, A.R.E.1
Drake, A.F.2
Gibson, S.E.3
Rendell, J.T.4
-
29
-
-
0003979828
-
-
Academic Press, San Diego
-
R. J. Sundberg, Indoles, Academic Press, San Diego, 1996.
-
(1996)
Indoles
-
-
Sundberg, R.J.1
-
30
-
-
77955039509
-
-
2, 1 exhibited approximately 50% deprotonation, whereas 3 was only 10% deprotonated.
-
2, 1 exhibited approximately 50% deprotonation, whereas 3 was only 10% deprotonated.
-
-
-
-
31
-
-
77955024167
-
-
CCDC 775771 (1.0) and 765716 (27b) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
-
CCDC 775771 (1.0) and 765716 (27b) 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
-
-
-
-
33
-
-
1542530938
-
-
B. Lantaño, J. Aguirre, M. L. Finkielsztein, E. Alesso, E. Brunet, G. Y. Moltrasio, Synth. Commun. 2004, 34, 625.
-
(2004)
Synth. Commun.
, vol.34
, pp. 625
-
-
Lantaño, B.1
Aguirre, J.2
Finkielsztein, M.L.3
Alesso, E.4
Brunet, E.5
Moltrasio, G.Y.6
-
34
-
-
77955037801
-
-
Alternatively, the coordinated arene can be purified first and then simply decomplexed by exposure to light and air. A solution of coordinated arene 2 a exposed to light and air provided triphenylmethane in 98% isolated yield.
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Alternatively, the coordinated arene can be purified first and then simply decomplexed by exposure to light and air. A solution of coordinated arene 2 a exposed to light and air provided triphenylmethane in 98% isolated yield.
-
-
-
-
35
-
-
0036643455
-
-
For cross-coupling reactions with organolithium reagents see : S.I. Murahashi, J. Organomet. Chem. 2002, 653, 27.
-
(2002)
J. Organomet. Chem.
, vol.653
, pp. 27
-
-
Murahashi, S.I.1
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