-
2
-
-
0032542329
-
-
P.H. Reggio, S. Basu-Dutt, J. Barnett-Norris, M.T. Castro, D.P. Hurst, H.H. Seltzman, M.J. Roche, A.F. Gilliman, B.F. Thomas, L.A. Stevenson, R.G. Pertwee, and M.E. Abood J. Med. Chem. 41 1998 5177 5187
-
(1998)
J. Med. Chem.
, vol.41
, pp. 5177-5187
-
-
Reggio, P.H.1
Basu-Dutt, S.2
Barnett-Norris, J.3
Castro, M.T.4
Hurst, D.P.5
Seltzman, H.H.6
Roche, M.J.7
Gilliman, A.F.8
Thomas, B.F.9
Stevenson, L.A.10
Pertwee, R.G.11
Abood, M.E.12
-
3
-
-
2342446618
-
-
H. Yu, I.J. Kim, J.E. Folk, X. Tian, R.B. Rothman, M.H. Baumann, C.M. Dersch, J.L. Flippen-Anderson, D. Parrish, A.E. Jacobson, and K.C. Rice J. Med. Chem. 47 2004 2624 2634
-
(2004)
J. Med. Chem.
, vol.47
, pp. 2624-2634
-
-
Yu, H.1
Kim, I.J.2
Folk, J.E.3
Tian, X.4
Rothman, R.B.5
Baumann, M.H.6
Dersch, C.M.7
Flippen-Anderson, J.L.8
Parrish, D.9
Jacobson, A.E.10
Rice, K.C.11
-
5
-
-
53649108973
-
-
E. Alcalde, N. Mesquida, J. Frigola, S. López-Pérez, and R. Merc Org. Biomol. Chem. 6 2008 3795 3810
-
(2008)
Org. Biomol. Chem.
, vol.6
, pp. 3795-3810
-
-
Alcalde, E.1
Mesquida, N.2
Frigola, J.3
López-Pérez, S.4
Merc, R.5
-
10
-
-
3042780057
-
-
For selective examples for the synthesis of indene derivatives, see
-
For selective examples for the synthesis of indene derivatives, see: M. Lautens, and T. Marquardt J. Org. Chem. 69 2004 4607 4614
-
(2004)
J. Org. Chem.
, vol.69
, pp. 4607-4614
-
-
Lautens, M.1
Marquardt, T.2
-
16
-
-
77953936776
-
-
A. Martínez, P. García-García, M.A. Fernández-Rodríguez, F. Rodríguz, and R. Sanz Angew. Chem., Int. Ed. 49 2010 4633 4637
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, pp. 4633-4637
-
-
Martínez, A.1
García-García, P.2
Fernández- Rodríguez, M.A.3
Rodríguz, F.4
Sanz, R.5
-
23
-
-
69949154156
-
-
S. Ye, K. Gao, H. Zhou, X. Yang, and J. Wu Chem. Commun. 2009 5406 5408
-
(2009)
Chem. Commun.
, pp. 5406-5408
-
-
Ye, S.1
Gao, K.2
Zhou, H.3
Yang, X.4
Wu, J.5
-
24
-
-
77957660310
-
-
R. Sanz, A. Martíguez, P. García-García, M.A. Fernández-Rodríguez, M.A. Rashid, and F. Rodríguez Chem. Commun. 46 2010 7427 7429
-
(2010)
Chem. Commun.
, vol.46
, pp. 7427-7429
-
-
Sanz, R.1
Martíguez, A.2
García-García, P.3
Fernández-Rodríguez, M.A.4
Rashid, M.A.5
Rodríguez, F.6
-
25
-
-
79952138347
-
-
Y. Zhu, G. Yin, D. Hong, P. Lu, and Y. Wang Org. Lett. 13 2011 1024 1027
-
(2011)
Org. Lett.
, vol.13
, pp. 1024-1027
-
-
Zhu, Y.1
Yin, G.2
Hong, D.3
Lu, P.4
Wang, Y.5
-
26
-
-
0035657514
-
-
For comprehensive reviews, see
-
For comprehensive reviews, see: B. Xu, and S. Ma Chin. J. Org. Chem. 21 2001 252 262
-
(2001)
Chin. J. Org. Chem.
, vol.21
, pp. 252-262
-
-
Xu, B.1
Ma, S.2
-
33
-
-
0031659740
-
-
For selected examples, see
-
For selected examples, see: R. Neidlein, and M. Winter Synthesis 1998 1362 1366
-
(1998)
Synthesis
, pp. 1362-1366
-
-
Neidlein, R.1
Winter, M.2
-
37
-
-
23944442185
-
-
For selected examples, see
-
For selected examples, see: Y.-Q. Fang, and M. Lautens Org. Lett. 7 2005 3549 3552
-
(2005)
Org. Lett.
, vol.7
, pp. 3549-3552
-
-
Fang, Y.-Q.1
Lautens, M.2
-
44
-
-
77953120839
-
-
K. Tao, J. Zheng, Z. Liu, W. Shen, and J. Zhang Tetrahedron Lett. 51 2010 3246 3249
-
(2010)
Tetrahedron Lett.
, vol.51
, pp. 3246-3249
-
-
Tao, K.1
Zheng, J.2
Liu, Z.3
Shen, W.4
Zhang, J.5
-
48
-
-
77955828687
-
-
Similarly, iodo is tolerated in the analogous indole preparation
-
Similarly, iodo is tolerated in the analogous indole preparation: S.G. Newman, and M. Lautens J. Am. Chem. Soc. 132 2010 11416 11417
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 11416-11417
-
-
Newman, S.G.1
Lautens, M.2
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