-
6
-
-
84864035835
-
-
S. Ma, Wiley-VCH Verlag GmbH & Co. Weinheim Chapter 21
-
R. Hayashi, and G.R. Cook S. Ma, Handbook of Cyclization Reactions Vol. 2 2010 Wiley-VCH Verlag GmbH & Co. Weinheim 1025 Chapter 21
-
(2010)
Handbook of Cyclization Reactions
, vol.2
, pp. 1025
-
-
Hayashi, R.1
Cook, G.R.2
-
7
-
-
0038907538
-
-
Intermolecular examples have also been reported, especially utilizing styrene derivatives
-
Intermolecular examples have also been reported, especially utilizing styrene derivatives: I. Shimizu, K.M. Khien, M. Nagatomo, T. Nakajima, and A. Yamamoto Chem. Lett. 1997 851
-
(1997)
Chem. Lett.
, pp. 851
-
-
Shimizu, I.1
Khien, K.M.2
Nagatomo, M.3
Nakajima, T.4
Yamamoto, A.5
-
8
-
-
30944469670
-
-
J. Kischel, I. Jovel, K. Mertins, A. Zapf, and M. Beller Org. Lett. 8 2006 19
-
(2006)
Org. Lett.
, vol.8
, pp. 19
-
-
Kischel, J.1
Jovel, I.2
Mertins, K.3
Zapf, A.4
Beller, M.5
-
22
-
-
84864061234
-
-
AP-1, or NF-κB activity for use as antiobesity, antidiabetic, antiinflammatory, or immunomodulatory agents WO2007/073503 A2 June 28, 2007
-
Duan, J.; Jiang, B. Preparation of indanes as modulators of glucocorticoid receptor, AP-1, or NF-κB activity for use as antiobesity, antidiabetic, antiinflammatory, or immunomodulatory agents WO2007/073503 A2 June 28, 2007.
-
Preparation of Indanes As Modulators of Glucocorticoid Receptor
-
-
Duan, J.1
Jiang, B.2
-
23
-
-
47349103796
-
-
H.O. Saxena, U. Faridi, S. Srivastava, J.K. Kumar, M.P. Karokar, S. Luqman, C.S. Chanotiya, V. Krishna, A.S. Negi, and S.P.S. Khanuja Bioorg. Med. Chem. Lett. 18 2008 3914
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 3914
-
-
Saxena, H.O.1
Faridi, U.2
Srivastava, S.3
Kumar, J.K.4
Karokar, M.P.5
Luqman, S.6
Chanotiya, C.S.7
Krishna, V.8
Negi, A.S.9
Khanuja, S.P.S.10
-
24
-
-
0037048663
-
-
B.D. Dangel, K. Godula, S.W. Youn, B. Sezen, and D. Sames J. Am. Chem. Soc. 124 2002 11856
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 11856
-
-
Dangel, B.D.1
Godula, K.2
Youn, S.W.3
Sezen, B.4
Sames, D.5
-
25
-
-
71149104734
-
-
Y. Dong, Q. Shi, K. Nakagawa-Goto, P.-C. Wu, K.F. Bastow, S.L. Morris-Natsche, and K.-H. Lee Bioorg. Med. Chem. Lett. 19 2009 6289
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 6289
-
-
Dong, Y.1
Shi, Q.2
Nakagawa-Goto, K.3
Wu, P.-C.4
Bastow, K.F.5
Morris-Natsche, S.L.6
Lee, K.-H.7
-
26
-
-
70349769741
-
-
B. Han, Z.-Q. He, J.-L. Li, R. Li, K. Jiang, T.-Y. Liu, and Y.-C. Chen Angew. Chem., Int. Ed. 48 2009 5474
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 5474
-
-
Han, B.1
He, Z.-Q.2
Li, J.-L.3
Li, R.4
Jiang, K.5
Liu, T.-Y.6
Chen, Y.-C.7
-
27
-
-
84864061235
-
-
WO2009/063061 A2 May 22
-
Himmelsbach, F.; Eckhardt, M.; Hamilton, B. S.; Heckel, A.; Kley, J.; Lehmann-Lintz, R.; Nar, H.; Peters, S.; Schuler-Metz, A.; Zentgraf, M. WO2009/063061 A2 May 22, 2009.
-
(2009)
-
-
Himmelsbach, F.1
Eckhardt, M.2
Hamilton, B.S.3
Heckel, A.4
Kley, J.5
Lehmann-Lintz, R.6
Nar, H.7
Peters, S.8
Schuler-Metz, A.9
Zentgraf, M.10
-
29
-
-
78149451765
-
-
K.N. Singh, P. Singh, A.K. Sharma, P. Sigh, and S.V. Kessar Synth. Commun. 40 2011 3716
-
(2011)
Synth. Commun.
, vol.40
, pp. 3716
-
-
Singh, K.N.1
Singh, P.2
Sharma, A.K.3
Sigh, P.4
Kessar, S.V.5
-
31
-
-
77955421936
-
-
K. Xie, S. Wang, P. Li, X. Li, Z. Yang, X. An, C.-C. Guo, and Z. Tan Tetrahedron Lett. 51 2010 4466
-
(2010)
Tetrahedron Lett.
, vol.51
, pp. 4466
-
-
Xie, K.1
Wang, S.2
Li, P.3
Li, X.4
Yang, Z.5
An, X.6
Guo, C.-C.7
Tan, Z.8
-
35
-
-
79960302019
-
-
As an example, it is quite possible that TfOH is the active catalyst in this system
-
As an example, it is quite possible that TfOH is the active catalyst in this system: B. Cacciuttolo, S. Poulain-Martini, and E. Duñach Eur. J. Org. Chem. 2011 3710
-
(2011)
Eur. J. Org. Chem.
, pp. 3710
-
-
Cacciuttolo, B.1
Poulain-Martini, S.2
Duñach, E.3
-
42
-
-
33749000858
-
-
D.C. Rosenfeld, S. Shekhar, A. Takemiya, M. Utsunomiya, and J.F. Hartwig Org. Lett. 8 2006 4179
-
(2006)
Org. Lett.
, vol.8
, pp. 4179
-
-
Rosenfeld, D.C.1
Shekhar, S.2
Takemiya, A.3
Utsunomiya, M.4
Hartwig, J.F.5
-
44
-
-
3142757194
-
-
M.J. Earle, U. Hakala, B.J. McAuley, M. Nieuwenhuyzen, A. Ramania, and K.R. Seddona Chem. Commun. 2004 1368
-
(2004)
Chem. Commun.
, pp. 1368
-
-
Earle, M.J.1
Hakala, U.2
McAuley, B.J.3
Nieuwenhuyzen, M.4
Ramania, A.5
Seddona, K.R.6
-
45
-
-
33749866364
-
-
P. Goodrich, C. Hardacre, H. Mehdi, P. Nancarrow, D.W. Rooney, and J.M. Thompson Ind. Eng. Chem. Res. 45 2006 6640
-
(2006)
Ind. Eng. Chem. Res.
, vol.45
, pp. 6640
-
-
Goodrich, P.1
Hardacre, C.2
Mehdi, H.3
Nancarrow, P.4
Rooney, D.W.5
Thompson, J.M.6
-
47
-
-
34147109763
-
-
Catalytic Friedel-Crafts alkylations utilizing alkene electrophiles and electron-deficient arenes are rare, and typically involve arene allylation by allylic halides or alcohols: R. Hayashi, and G.R. Cook Org. Lett. 9 2007 1311
-
(2007)
Org. Lett.
, vol.9
, pp. 1311
-
-
Hayashi, R.1
Cook, G.R.2
-
50
-
-
84890973385
-
-
L. Ackermann, Wiley-VCH Verlag GmbH & Co. Weinheim
-
A. Littke L. Ackermann, Modern Arylation Methods 2009 Wiley-VCH Verlag GmbH & Co. Weinheim 25
-
(2009)
Modern Arylation Methods
, pp. 25
-
-
Littke, A.1
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