-
1
-
-
0032101265
-
-
Su, J.-Y., Xu, X.-H., Zeng, L.-M., Wang, M.-Y., Lu, N., Lu, Y., and Zhang, Q.-T. Phytochemistry 1998, 48, 583-584
-
(1998)
Phytochemistry
, vol.48
, pp. 583-584
-
-
Su, J.-Y.1
Xu, X.-H.2
Zeng, L.-M.3
Wang, M.-Y.4
Lu, N.5
Lu, Y.6
Zhang, Q.-T.7
-
2
-
-
33646537465
-
-
Kelly, T. R., Elliott, E. L., Lebedev, R., and Pagalday, J. J. Am. Chem. Soc. 2006, 128, 5646-5647
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 5646-5647
-
-
Kelly, T.R.1
Elliott, E.L.2
Lebedev, R.3
Pagalday, J.4
-
6
-
-
70449345550
-
-
14th ed.;, Ed.; Merck Publishing
-
The Merck Index, 14th ed.; O'Neil, M. J., Ed.; Merck Publishing, 2006.
-
(2006)
The Merck Index
-
-
O'Neil, M.J.1
-
9
-
-
45149106841
-
-
Kennedy, J. P., Williams, L., Bridges, T. M., Daniels, R. N., Weaver, D., and Lindsley, C. W. J. Comb. Chem. 2008, 10, 345-354
-
(2008)
J. Comb. Chem.
, vol.10
, pp. 345-354
-
-
Kennedy, J.P.1
Williams, L.2
Bridges, T.M.3
Daniels, R.N.4
Weaver, D.5
Lindsley, C.W.6
-
10
-
-
38349176790
-
-
Lesch, B., Thomson, D. W., and Lindell, S. D. Comb. Chem. High Throughput Screening 2008, 11, 36-61
-
(2008)
Comb. Chem. High Throughput Screening
, vol.11
, pp. 36-61
-
-
Lesch, B.1
Thomson, D.W.2
Lindell, S.D.3
-
11
-
-
67049134276
-
-
Nandy, J. P., Prakesch, M., Khadem, S., Reddy, P. T., Sharma, U., and Arya, P. Chem. Rev 2009, 109, 1999-2060
-
(2009)
Chem. Rev
, vol.109
, pp. 1999-2060
-
-
Nandy, J.P.1
Prakesch, M.2
Khadem, S.3
Reddy, P.T.4
Sharma, U.5
Arya, P.6
-
12
-
-
66349092738
-
-
Lindell, S. D., Pattenden, L. C., and Shannon, J. Bioorg. Med. Chem. 2009, 17, 4035-4046
-
(2009)
Bioorg. Med. Chem.
, vol.17
, pp. 4035-4046
-
-
Lindell, S.D.1
Pattenden, L.C.2
Shannon, J.3
-
13
-
-
70349479418
-
-
Dolle, R. E., Le Bourdonnec, B., Goodman, A. J., Morales, G. A., Thomas, C. J., and Zhang, W. J. Comb. Chem. 2009, 11, 739-790
-
(2009)
J. Comb. Chem.
, vol.11
, pp. 739-790
-
-
Dolle, R.E.1
Le Bourdonnec, B.2
Goodman, A.J.3
Morales, G.A.4
Thomas, C.J.5
Zhang, W.6
-
14
-
-
0001870892
-
-
Dudfield, P. J., Le, V.-D., Lindell, S. D., and Rees, C. W. J. Chem. Soc., Perkin 1 1999, 20, 2929-2936
-
(1999)
Chem. Soc., Perkin 1
, vol.20
, pp. 2929-2936
-
-
Dudfield, P.J.1
Le, V.-D.2
Lindell, S.D.3
Rees, C.W.J.4
-
15
-
-
78149318739
-
-
PCT Int. Appl. WO 2009/132123 A1
-
Cho, A., Kim, C. U., and Parrish, J. PCT Int. Appl. WO 2009/132123 A1, 2009.
-
(2009)
-
-
Cho, A.1
Kim, C.U.2
Parrish, J.3
-
16
-
-
32044440715
-
-
Goodacre, S. C., Hallett, D. J., Carling, R. W., Castro, J. L., Reynolds, D. S., Pike, A., Wafford, K. A., Newman, R., Atack, J. R., and Street, L. J. Bioorg. Med. Chem. Lett. 2006, 16, 1582-1585
-
(2006)
Bioorg. Med. Chem. Lett.
, vol.16
, pp. 1582-1585
-
-
Goodacre, S.C.1
Hallett, D.J.2
Carling, R.W.3
Castro, J.L.4
Reynolds, D.S.5
Pike, A.6
Wafford, K.A.7
Newman, R.8
Atack, J.R.9
Street, L.J.10
-
17
-
-
78149287632
-
-
PCT Int. Appl. WO 2010/014930 A2
-
Babu, Y. S., Chand, P., Kotian, P. L., and Kumar, S. PCT Int. Appl. WO 2010/014930 A2, 2010.
-
(2010)
-
-
Babu, Y.S.1
Chand, P.2
Kotian, P.L.3
Kumar, S.4
-
18
-
-
78149344976
-
-
U.S. Pat. Appl. US 2004/0220189 A1
-
Sun, C. L., Liang, C., Huang, P., Harris, G. D., and Guan, H. U.S. Pat. Appl. US 2004/0220189 A1, 2004.
-
(2004)
-
-
Sun, C.L.1
Liang, C.2
Huang, P.3
Harris, G.D.4
Guan, H.5
-
19
-
-
78149335228
-
-
U.S. Pat. Appl. US 2005/0009832 A1
-
Sun, C. L., Liang, C., Huang, P., Harris, G. D., and Guan, H. U.S. Pat. Appl. US 2005/0009832 A1, 2005.
-
(2005)
-
-
Sun, C.L.1
Liang, C.2
Huang, P.3
Harris, G.D.4
Guan, H.5
-
21
-
-
33846918696
-
-
For a recent review on the direct arylation reaction, see
-
For a recent review on the direct arylation reaction, see: Alberico, D., Scot, M. E., and Lautens, M. Chem. Rev. 2007, 107, 174-238
-
(2007)
Chem. Rev.
, vol.107
, pp. 174-238
-
-
Alberico, D.1
Scot, M.E.2
Lautens, M.3
-
22
-
-
0003397781
-
-
Wiley-VCH: Weinheim, Germany ISBN 3-527-29421-X
-
Metal-Catalyzed Cross-Coupling Reactions; Diederich, F. and Stang, P. J., Eds.; Wiley-VCH: Weinheim, Germany, 1998; Vol. XXI, 517 pp, ISBN 3-527-29421-X.
-
(1998)
Metal-Catalyzed Cross-Coupling Reactions
, vol.21
, pp. 517
-
-
Diederich, F.1
Stang, P.J.2
-
25
-
-
33748243831
-
-
Nicolaou, K. C., Xiao, X. Y., Parandoosh, Z., Senyei, A., and Nova, M. P. Angew. Chem., Int. Ed. Engl. 1995, 34, 2289-2291
-
(1995)
Angew. Chem., Int. Ed. Engl.
, vol.34
, pp. 2289-2291
-
-
Nicolaou, K.C.1
Xiao, X.Y.2
Parandoosh, Z.3
Senyei, A.4
Nova, M.P.5
-
26
-
-
0028815228
-
-
Moran, E. J., Sarshar, S., Carghill, J. F., Shahbaz, M. M., Lio, A., Mjalli, A. M. M., and Armstrong, R. W. J. Am. Chem. Soc. 1995, 117, 10787-10788
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 10787-10788
-
-
Moran, E.J.1
Sarshar, S.2
Carghill, J.F.3
Shahbaz, M.M.4
Lio, A.5
Mjalli, A.M.M.6
Armstrong, R.W.7
-
27
-
-
0034263910
-
-
Herpin, T. F., Van Kirk, K. G., Salvino, J. M., Yu, S. T., and Labaudiniere, R. F. J. Comb. Chem. 2000, 2, 513-521
-
(2000)
J. Comb. Chem.
, vol.2
, pp. 513-521
-
-
Herpin, T.F.1
Van Kirk, K.G.2
Salvino, J.M.3
Yu, S.T.4
Labaudiniere, R.F.5
-
28
-
-
0141563694
-
-
Guo, G., Arvanitis, E. A., Pottorf, R. S., and Player, M. R. J. Comb. Chem. 2003, 5, 408-413
-
(2003)
J. Comb. Chem.
, vol.5
, pp. 408-413
-
-
Guo, G.1
Arvanitis, E.A.2
Pottorf, R.S.3
Player, M.R.4
-
29
-
-
33745725794
-
-
Wan, Z.-K., Wacharasindu, S., Binnun, E., and Mansour, T. Org. Lett. 2006, 8, 2425-2428
-
(2006)
Org. Lett.
, vol.8
, pp. 2425-2428
-
-
Wan, Z.-K.1
Wacharasindu, S.2
Binnun, E.3
Mansour, T.4
-
30
-
-
77956536452
-
-
Lindell, S. D., Maechling, S., and Sabina, R. L. ACS Med. Chem. Lett. 2010, 1, 286
-
(2010)
ACS Med. Chem. Lett.
, vol.1
, pp. 286
-
-
Lindell, S.D.1
Maechling, S.2
Sabina, R.L.3
-
31
-
-
78149314251
-
-
See Supporting Information for full details
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See Supporting Information for full details.
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-
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32
-
-
78149326821
-
-
Unpublished results
-
Maechling, S., Haupt, S., Lindell, S. D., and Wahedi, S. A. Unpublished results.
-
-
-
Maechling, S.1
Haupt, S.2
Lindell, S.D.3
Wahedi, S.A.4
-
33
-
-
78149331685
-
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2 group of compound 2 is replaced by a morpholino group; then the palladium catalysed direct arylation reaction proceeds smoothly with aryl bromide 15 { 1 } to give the expected product in 62% yield after chromatography. Unpublished results
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2 group of compound 2 is replaced by a morpholino group; then the palladium catalysed direct arylation reaction proceeds smoothly with aryl bromide 15 { 1 } to give the expected product in 62% yield after chromatography. Maechling, S. and Lindell, S. D. Unpublished results.
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Maechling, S.1
Lindell, S.D.2
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