-
1
-
-
0034249671
-
-
For some selected examples of Mizoroki-Heck reaction with aryl halides, see: I.P. Beletskaya, and A.V. Cheprakov Chem. Rev. 100 2000 3009 3066
-
(2000)
Chem. Rev.
, vol.100
, pp. 3009-3066
-
-
Beletskaya, I.P.1
Cheprakov, A.V.2
-
3
-
-
0037419139
-
-
V. Calo, A. Nacci, A. Monopoli, S. Laera, and N. Cioffi J. Org. Chem. 68 2003 2929 2933
-
(2003)
J. Org. Chem.
, vol.68
, pp. 2929-2933
-
-
Calo, V.1
Nacci, A.2
Monopoli, A.3
Laera, S.4
Cioffi, N.5
-
4
-
-
70349929413
-
-
V. Calo, A. Nacci, A. Monopoli, and P. Cotugno Angew. Chem., Int. Ed. 48 2009 6101 6103
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 6101-6103
-
-
Calo, V.1
Nacci, A.2
Monopoli, A.3
Cotugno, P.4
-
9
-
-
79952677383
-
-
For some selected examples of Fujiwara-Moritani reaction with arenes, see: J.L. Bras, and J. Muzart Chem. Rev. 111 2011 1170 1214
-
(2011)
Chem. Rev.
, vol.111
, pp. 1170-1214
-
-
Bras, J.L.1
Muzart, J.2
-
12
-
-
77955169796
-
-
B. Karimi, H. Behzadnia, D. Elhamifar, P.F. Akhavan, F.K. Esfahani, and A. Zamani Synthesis 2010 1399 1427
-
(2010)
Synthesis
, pp. 1399-1427
-
-
Karimi, B.1
Behzadnia, H.2
Elhamifar, D.3
Akhavan, P.F.4
Esfahani, F.K.5
Zamani, A.6
-
18
-
-
84859524880
-
-
For some selected examples on the synthesis of highly-substituted olefins, see: Z. He, S. Kirchberg, R. Frohlich, and A. Studer Angew. Chem., Int. Ed. 51 2012 3699 3702
-
(2012)
Angew. Chem., Int. Ed.
, vol.51
, pp. 3699-3702
-
-
He, Z.1
Kirchberg, S.2
Frohlich, R.3
Studer, A.4
-
24
-
-
24744458162
-
-
M. Shimizu, C. Nakamaki, K. Shimono, M. Schelper, T. Kurahashi, and T. Hiyama J. Am. Chem. Soc. 127 2005 12506 12507
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 12506-12507
-
-
Shimizu, M.1
Nakamaki, C.2
Shimono, K.3
Schelper, M.4
Kurahashi, T.5
Hiyama, T.6
-
27
-
-
80052474735
-
-
Y. Nishihara, Y. Okada, J. Jiao, M. Suetsugu, M.-T. Lan, M. Kinoshita, M. Iwasaki, and K. Takagi Angew. Chem., Int. Ed. 50 2011 8660 8664
-
(2011)
Angew. Chem., Int. Ed.
, vol.50
, pp. 8660-8664
-
-
Nishihara, Y.1
Okada, Y.2
Jiao, J.3
Suetsugu, M.4
Lan, M.-T.5
Kinoshita, M.6
Iwasaki, M.7
Takagi, K.8
-
29
-
-
77956570131
-
-
E. Brachet, A. Hamze, J.-F. Peyrat, J.-D. Brion, and M. Alami Org. Lett. 12 2010 4042 4045
-
(2010)
Org. Lett.
, vol.12
, pp. 4042-4045
-
-
Brachet, E.1
Hamze, A.2
Peyrat, J.-F.3
Brion, J.-D.4
Alami, M.5
-
32
-
-
70449393366
-
-
C.M. Nunes, J. Limberger, S. Poersch, M. Seferin, and A.L. Monteiro Synthesis 2009 2761 2765
-
(2009)
Synthesis
, pp. 2761-2765
-
-
Nunes, C.M.1
Limberger, J.2
Poersch, S.3
Seferin, M.4
Monteiro, A.L.5
-
33
-
-
0032474915
-
-
For the biological activity of 3-alkylidene-oxindole derivatives, see: L. Sun, N. Tran, F. Tang, H. App, P. Hirth, G. McMahon, and C. Tang J. Med. Chem. 41 1998 2588 2603
-
(1998)
J. Med. Chem.
, vol.41
, pp. 2588-2603
-
-
Sun, L.1
Tran, N.2
Tang, F.3
App, H.4
Hirth, P.5
McMahon, G.6
Tang, C.7
-
34
-
-
80052086220
-
-
M. Arthuis, R. Pontikis, G.G. Chabot, J. Seguin, L. Quentin, S. Bourg, L. Morin-Allory, and J.-C. Florent ChemMedChem 6 2011 1693 1705
-
(2011)
ChemMedChem
, vol.6
, pp. 1693-1705
-
-
Arthuis, M.1
Pontikis, R.2
Chabot, G.G.3
Seguin, J.4
Quentin, L.5
Bourg, S.6
Morin-Allory, L.7
Florent, J.-C.8
-
36
-
-
84863341752
-
-
T. Zou, X.-G. Zhang, J.-H. Li, C.-L. Deng, and R.-Y. Tang Adv. Synth. Catal. 354 2012 889 898
-
(2012)
Adv. Synth. Catal.
, vol.354
, pp. 889-898
-
-
Zou, T.1
Zhang, X.-G.2
Li, J.-H.3
Deng, C.-L.4
Tang, R.-Y.5
-
37
-
-
7144261702
-
-
Y. Muranaka, Y. Yamasaki, Y. Nozawa, H. Terakawa, Y. Tanahashi, N. Oda, A. Satoh, T. Asao, H. Miyake, and N. Matsuura J. Pharmacol. Exp. Ther. 285 1998 1280 1286
-
(1998)
J. Pharmacol. Exp. Ther.
, vol.285
, pp. 1280-1286
-
-
Muranaka, Y.1
Yamasaki, Y.2
Nozawa, Y.3
Terakawa, H.4
Tanahashi, Y.5
Oda, N.6
Satoh, A.7
Asao, T.8
Miyake, H.9
Matsuura, N.10
-
38
-
-
0038246451
-
-
M. Kinoshita, K. Baba, A. Nagayasu, K. Yamabe, M. Azuma, H. Houchi, and K. Minakuchi Drug Dev. Ind. Pharm. 29 2003 523 529
-
(2003)
Drug Dev. Ind. Pharm.
, vol.29
, pp. 523-529
-
-
Kinoshita, M.1
Baba, K.2
Nagayasu, A.3
Yamabe, K.4
Azuma, M.5
Houchi, H.6
Minakuchi, K.7
-
39
-
-
84870459366
-
-
WO 2011/032320, 2011
-
Nan, F.; Yu, L.; Zhang, M.; Chen, L.; Huang, M.; Feng, L.; Li, J.; Pang, T. WO 2011/032320, 2011; Chem. Abstr. 2011, 154, 360856.
-
(2011)
Chem. Abstr.
, vol.154
, pp. 360856
-
-
Nan, F.1
Yu, L.2
Zhang, M.3
Chen, L.4
Huang, M.5
Feng, L.6
Li, J.7
Pang, T.8
-
40
-
-
84870469648
-
-
WO 2005/058309, 2005
-
Bouerat, L. M. E.; Fensholdt, J.; Nielsen, S. F.; Liang, X.; Havez, S. E.; Andersson, E. C.; Jensen, L.; Hansen, J. R. WO 2005/058309, 2005; Chem. Abstr. 2005, 143, 97259.
-
(2005)
Chem. Abstr.
, vol.143
, pp. 97259
-
-
Bouerat, L.M.E.1
Fensholdt, J.2
Nielsen, S.F.3
Liang, X.4
Havez, S.E.5
Andersson, E.C.6
Jensen, L.7
Hansen, J.R.8
-
41
-
-
77955674388
-
-
For the synthesis and synthetic applications of 3-alkylidene-oxindole derivatives, see: A. Millemaggi, and R.J.K. Taylor Eur. J. Org. Chem. 2010 4527 4547 and further references cited therein
-
(2010)
Eur. J. Org. Chem.
, pp. 4527-4547
-
-
Millemaggi, A.1
Taylor, R.J.K.2
-
42
-
-
84855921171
-
-
G. Rassu, V. Zambrano, R. Tanca, A. Sartori, L. Battistini, F. Zanardi, C. Curti, and G. Casiraghi Eur. J. Org. Chem. 2012 466 470
-
(2012)
Eur. J. Org. Chem.
, pp. 466-470
-
-
Rassu, G.1
Zambrano, V.2
Tanca, R.3
Sartori, A.4
Battistini, L.5
Zanardi, F.6
Curti, C.7
Casiraghi, G.8
-
46
-
-
33750346700
-
-
For the synthesis of 3-alkylidene-oxindoles via a palladium-catalyzed arylation process, see: A. Pinto, L. Neuville, P. Retailleau, and J. Zhu Org. Lett. 8 2006 4927 4930
-
(2006)
Org. Lett.
, vol.8
, pp. 4927-4930
-
-
Pinto, A.1
Neuville, L.2
Retailleau, P.3
Zhu, J.4
-
52
-
-
70449631391
-
-
T.-S. Jiang, R.-Y. Tang, X.-G. Zhang, X.-H. Li, and J.-H. Li J. Org. Chem. 74 2009 8834 8837
-
(2009)
J. Org. Chem.
, vol.74
, pp. 8834-8837
-
-
Jiang, T.-S.1
Tang, R.-Y.2
Zhang, X.-G.3
Li, X.-H.4
Li, J.-H.5
-
55
-
-
27544445308
-
-
R. Yanada, S. Obika, Y. Kobayashi, T. Inokuma, M. Oyama, K. Yanada, and Y. Takemoto Adv. Synth. Catal. 347 2005 1632 1642
-
(2005)
Adv. Synth. Catal.
, vol.347
, pp. 1632-1642
-
-
Yanada, R.1
Obika, S.2
Kobayashi, Y.3
Inokuma, T.4
Oyama, M.5
Yanada, K.6
Takemoto, Y.7
-
56
-
-
23644439576
-
-
R. Yanada, S. Obika, T. Inokuma, K. Yanada, M. Yamashita, S. Ohta, and Y. Takemoto J. Org. Chem. 70 2005 6972 6975
-
(2005)
J. Org. Chem.
, vol.70
, pp. 6972-6975
-
-
Yanada, R.1
Obika, S.2
Inokuma, T.3
Yanada, K.4
Yamashita, M.5
Ohta, S.6
Takemoto, Y.7
-
57
-
-
80054737034
-
-
S. Balalaie, H. Motaghedi, M. Bararjanian, D. Tahmassebi, and H.R. Bijanzadeh Tetrahedron 67 2011 9134 9141
-
(2011)
Tetrahedron
, vol.67
, pp. 9134-9141
-
-
Balalaie, S.1
Motaghedi, H.2
Bararjanian, M.3
Tahmassebi, D.4
Bijanzadeh, H.R.5
-
58
-
-
77951826645
-
-
M. Bararjanian, S. Balalaie, F. Rominger, B. Movassagh, and H.R. Bijanzadeh J. Org. Chem. 75 2010 2806 2812
-
(2010)
J. Org. Chem.
, vol.75
, pp. 2806-2812
-
-
Bararjanian, M.1
Balalaie, S.2
Rominger, F.3
Movassagh, B.4
Bijanzadeh, H.R.5
-
62
-
-
28744455408
-
-
S. Kamijo, Y. Sasaki, C. Kanazawa, T. Schusseler, and Y. Yamamoto Angew. Chem., Int. Ed. 44 2005 7718 7721
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 7718-7721
-
-
Kamijo, S.1
Sasaki, Y.2
Kanazawa, C.3
Schusseler, T.4
Yamamoto, Y.5
-
63
-
-
48249110557
-
-
S. Tang, P. Peng, Z.-Q. Wang, B.-X. Tang, C.-L. Deng, J.-H. Li, P. Zhong, and N.-X. Wang Org. Lett. 10 2008 1875 1878
-
(2008)
Org. Lett.
, vol.10
, pp. 1875-1878
-
-
Tang, S.1
Peng, P.2
Wang, Z.-Q.3
Tang, B.-X.4
Deng, C.-L.5
Li, J.-H.6
Zhong, P.7
Wang, N.-X.8
-
64
-
-
45549107152
-
-
S. Tang, P. Peng, S.-F. Pi, Y. Liang, N.-X. Wang, and J.-H. Li Org. Lett. 10 2008 1179 1182
-
(2008)
Org. Lett.
, vol.10
, pp. 1179-1182
-
-
Tang, S.1
Peng, P.2
Pi, S.-F.3
Liang, Y.4
Wang, N.-X.5
Li, J.-H.6
-
66
-
-
84865714120
-
-
H.S. Lee, K.H. Kim, S.H. Kim, and J.N. Kim Adv. Synth. Catal. 354 2012 2419 2426 and further references cited therein on the palladium-catalyzed chelation-assisted reactions for the purpose of stereo- and regio-control, and multiple arylations
-
(2012)
Adv. Synth. Catal.
, vol.354
, pp. 2419-2426
-
-
Lee, H.S.1
Kim, K.H.2
Kim, S.H.3
Kim, J.N.4
-
68
-
-
82355168631
-
-
(For 1a and 1b)
-
C. Palumbo, G. Mazzeo, A. Mazziotta, A. Gambacorta, M.A. Loreto, A. Migliorini, S. Superchi, D. Tofani, and T. Gasperi Org. Lett. 13 2011 6248 6251 (For 1a and 1b)
-
(2011)
Org. Lett.
, vol.13
, pp. 6248-6251
-
-
Palumbo, C.1
Mazzeo, G.2
Mazziotta, A.3
Gambacorta, A.4
Loreto, M.A.5
Migliorini, A.6
Superchi, S.7
Tofani, D.8
Gasperi, T.9
-
69
-
-
84555191597
-
-
(For 1c)
-
B. Tan, X. Zeng, W.W.Y. Leong, Z. Shi, C.F. Barbas III, and G. Zhong Chem. Eur. J. 18 2012 63 67 (For 1c)
-
(2012)
Chem. Eur. J.
, vol.18
, pp. 63-67
-
-
Tan, B.1
Zeng, X.2
Leong, W.W.Y.3
Shi, Z.4
Barbas Iii, C.F.5
Zhong, G.6
-
71
-
-
78249241499
-
-
(For 1e and 1k)
-
A. Voituriez, N. Pinto, M. Neel, P. Retailleau, and A. Marinetti Chem. Eur. J. 16 2010 12541 12544 (For 1e and 1k)
-
(2010)
Chem. Eur. J.
, vol.16
, pp. 12541-12544
-
-
Voituriez, A.1
Pinto, N.2
Neel, M.3
Retailleau, P.4
Marinetti, A.5
-
74
-
-
0033179825
-
-
For the stereo-mutation via an O-Pd intermediate, see: M. Ikeda, S.A.A. El Bialy, and T. Yakura Heterocycles 51 1999 1957 1970 and further references cited therein
-
(1999)
Heterocycles
, vol.51
, pp. 1957-1970
-
-
Ikeda, M.1
El Bialy, S.A.A.2
Yakura, T.3
-
75
-
-
33644508323
-
-
E.L. Cropper, A.J.P. White, A. Ford, and K.K. Hii J. Org. Chem. 71 2006 1732 1735 When we subjected the reaction mixture of 1a for a longer time (48 h) the ratio between 2a and 3a was not changed. In addition, we could not observe the formation of 3a in any trace amount when we subjected 2a to the palladium-catalyzed arylation reaction conditions. The results stated that the possibility for the Pd-catalyzed isomerization between 2a and 3a would be low
-
(2006)
J. Org. Chem.
, vol.71
, pp. 1732-1735
-
-
Cropper, E.L.1
White, A.J.P.2
Ford, A.3
Hii, K.K.4
-
76
-
-
2942643950
-
-
For the alkyl to aryl 1,4-palladium migration, see: Q. Huang, A. Fazio, G. Dai, M.A. Campo, and R.C. Larock J. Am. Chem. Soc. 126 2004 7460 7461
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 7460-7461
-
-
Huang, Q.1
Fazio, A.2
Dai, G.3
Campo, M.A.4
Larock, R.C.5
-
79
-
-
77954248100
-
-
For Pd(II)-catalyzed oxidation of α,β-position of carbonyl compounds, see: J. Muzart Eur. J. Org. Chem. 2010 3779 3790 and further references cited therein
-
(2010)
Eur. J. Org. Chem.
, pp. 3779-3790
-
-
Muzart, J.1
|