-
2
-
-
33744820579
-
-
G.C. Tron, T. Pirali, G. Sorba, F. Pagliai, S. Busacca, and A.A. Genazzani J. Med. Chem. 49 2006 3033 3044
-
(2006)
J. Med. Chem.
, vol.49
, pp. 3033-3044
-
-
Tron, G.C.1
Pirali, T.2
Sorba, G.3
Pagliai, F.4
Busacca, S.5
Genazzani, A.A.6
-
3
-
-
37349083149
-
-
A. Chaudhary, S.N. Pandeya, P. Kumar, P. Sharma, S. Gupta, N. Soni, K.K. Verma, and G. Bhardwaj Mini-Rev. Med. Chem. 7 2007 1186 1205
-
(2007)
Mini-Rev. Med. Chem.
, vol.7
, pp. 1186-1205
-
-
Chaudhary, A.1
Pandeya, S.N.2
Kumar, P.3
Sharma, P.4
Gupta, S.5
Soni, N.6
Verma, K.K.7
Bhardwaj, G.8
-
4
-
-
79851496869
-
-
Y. Shan, J. Zhang, Z. Liu, M. Wang, and Y. Dong Curr. Med. Chem. 18 2011 523 538
-
(2011)
Curr. Med. Chem.
, vol.18
, pp. 523-538
-
-
Shan, Y.1
Zhang, J.2
Liu, Z.3
Wang, M.4
Dong, Y.5
-
5
-
-
0024513175
-
-
G.R. Pettit, S.B. Singh, E. Hamel, C.M. Lin, D.S. Alberts, and D. Garcia-Kendall Experientia 45 1989 209 211
-
(1989)
Experientia
, vol.45
, pp. 209-211
-
-
Pettit, G.R.1
Singh, S.B.2
Hamel, E.3
Lin, C.M.4
Alberts, D.S.5
Garcia-Kendall, D.6
-
6
-
-
0029066847
-
-
G.R. Pettit, S.B. Singh, M.R. Boyd, E. Hamel, R.K. Pettit, J.M. Schmidt, and F. Hogan J. Med. Chem. 38 1995 1666 1672
-
(1995)
J. Med. Chem.
, vol.38
, pp. 1666-1672
-
-
Pettit, G.R.1
Singh, S.B.2
Boyd, M.R.3
Hamel, E.4
Pettit, R.K.5
Schmidt, J.M.6
Hogan, F.7
-
8
-
-
20444403700
-
-
cis CA-4 is 30 times more potent than its trans isomer for the inhibition of tubulin polymerization
-
cis CA-4 is 30 times more potent than its trans isomer for the inhibition of tubulin polymerization: G.R. Pettit, M.R. Rhodes, D.L. Herald, E. Hamel, J.M. Schmidt, and R.K. Pettit J. Med. Chem. 48 2005 4087 4099
-
(2005)
J. Med. Chem.
, vol.48
, pp. 4087-4099
-
-
Pettit, G.R.1
Rhodes, M.R.2
Herald, D.L.3
Hamel, E.4
Schmidt, J.M.5
Pettit, R.K.6
-
9
-
-
84869090557
-
-
T.T.B. Nguyen, T. Lomberget, N.C. Tran, E. Colomb, L. Nachtergaele, S. Thoret, J. Dubois, J. Guillaume, R. Abdayem, M. Haftek, and R. Barret Bioorg. Med. Chem. Lett. 22 2012 7227 7231
-
(2012)
Bioorg. Med. Chem. Lett.
, vol.22
, pp. 7227-7231
-
-
Nguyen, T.T.B.1
Lomberget, T.2
Tran, N.C.3
Colomb, E.4
Nachtergaele, L.5
Thoret, S.6
Dubois, J.7
Guillaume, J.8
Abdayem, R.9
Haftek, M.10
Barret, R.11
-
10
-
-
33751283824
-
-
For an example concerning the application of Wittig reaction for the preparation of CA-4 and derivatives, see Ref. 4. Some improvement of the diastereoselectivity of the Wittig reaction using cooperative ortho-effects has also been described
-
For an example concerning the application of Wittig reaction for the preparation of CA-4 and derivatives, see Ref. 4. Some improvement of the diastereoselectivity of the Wittig reaction using cooperative ortho-effects has also been described: D.C. Harrowven, I.L. Guy, M. Howell, and G. Packham Synlett 2006 2977 2980
-
(2006)
Synlett
, pp. 2977-2980
-
-
Harrowven, D.C.1
Guy, I.L.2
Howell, M.3
Packham, G.4
-
16
-
-
84860133384
-
-
Y.B. Malysheva, S. Combes, A.Y. Fedorov, P. Knochel, and A.E. Gavryushin Synlett 2012 1205 1208
-
(2012)
Synlett
, pp. 1205-1208
-
-
Malysheva, Y.B.1
Combes, S.2
Fedorov, A.Y.3
Knochel, P.4
Gavryushin, A.E.5
-
18
-
-
0035977227
-
-
K. Gaukroger, J.A. Hadfield, L.A. Hepworth, N.J. Lawrence, and A.T. McGown J. Org. Chem. 66 2001 8135 8138
-
(2001)
J. Org. Chem.
, vol.66
, pp. 8135-8138
-
-
Gaukroger, K.1
Hadfield, J.A.2
Hepworth, L.A.3
Lawrence, N.J.4
McGown, A.T.5
-
19
-
-
0033035311
-
-
This protocol derived from a methodology developed by Uenishi and co-workers
-
H.-G. Herz, M.J.R.P. Queiroz, and G. Maas Synthesis 6 1999 1013 1016 This protocol derived from a methodology developed by Uenishi and co-workers
-
(1999)
Synthesis
, vol.6
, pp. 1013-1016
-
-
Herz, H.-G.1
Queiroz, M.J.R.P.2
Maas, G.3
-
20
-
-
0030576985
-
-
J. Uenishi, R. Kawahama, Y. Shiga, O. Yonemitsu, and J. Tsuji Tetrahedron Lett. 37 1996 6759 6762
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 6759-6762
-
-
Uenishi, J.1
Kawahama, R.2
Shiga, Y.3
Yonemitsu, O.4
Tsuji, J.5
-
22
-
-
0032858830
-
-
For an example of the Sonogashira coupling reaction for the preparation of CA-4, see
-
For an example of the Sonogashira coupling reaction for the preparation of CA-4, see: N.J. Lawrence, F.A. Ghani, L.A. Hepworth, J.A. Hadfield, A.T. McGown, and R.G. Pritchard Synthesis 1999 1656 1660
-
(1999)
Synthesis
, pp. 1656-1660
-
-
Lawrence, N.J.1
Ghani, F.A.2
Hepworth, L.A.3
Hadfield, J.A.4
McGown, A.T.5
Pritchard, R.G.6
-
26
-
-
34547187077
-
-
For the preparation of 2-alkynyl indole and benzofuran derivatives using a tandem ring-closure/Sonogashira coupling sequence, see
-
For the preparation of 2-alkynyl indole and benzofuran derivatives using a tandem ring-closure/Sonogashira coupling sequence, see: M. Nagamochi, Y.-Q. Fang, and M. Lautens Org. Lett. 9 2007 2955 2958
-
(2007)
Org. Lett.
, vol.9
, pp. 2955-2958
-
-
Nagamochi, M.1
Fang, Y.-Q.2
Lautens, M.3
-
28
-
-
37549064279
-
-
J.-M. L'Helgoual'ch, A. Seggio, F. Chevallier, M. Yonehara, E. Jeanneau, M. Uchiyama, and F. Mongin J. Org. Chem. 73 2008 177 183
-
(2008)
J. Org. Chem.
, vol.73
, pp. 177-183
-
-
L'Helgoual'Ch, J.-M.1
Seggio, A.2
Chevallier, F.3
Yonehara, M.4
Jeanneau, E.5
Uchiyama, M.6
Mongin, F.7
-
30
-
-
0032510004
-
-
2-Iodo-indole was prepared with a 83% yield from the N-phenylsulfonyl precursor, following this protocol
-
2-Iodo-indole was prepared with a 83% yield from the N-phenylsulfonyl precursor, following this protocol: A. Yasuhara, and T. Sakamoto Tetrahedron Lett. 39 1998 595 596
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 595-596
-
-
Yasuhara, A.1
Sakamoto, T.2
-
31
-
-
69549118601
-
-
This approach was also extended for the preparation of 2-functionnalized benzo[b]thiophenes using a one-pot ring-closure/coupling reactions (Suzuki, Heck, Sonogashira) sequence
-
S.G. Newman, V. Aureggi, C.S. Bryan, and M. Lautens Chem. Commun. 2009 5236 5238 This approach was also extended for the preparation of 2-functionnalized benzo[b]thiophenes using a one-pot ring-closure/coupling reactions (Suzuki, Heck, Sonogashira) sequence
-
(2009)
Chem. Commun.
, pp. 5236-5238
-
-
Newman, S.G.1
Aureggi, V.2
Bryan, C.S.3
Lautens, M.4
-
33
-
-
0034752296
-
-
V. Cañibano, J.F. Rodríguez, M. Santos, M.A. Sanz-Tejedor, M.C. Carreño, G. González, and J.L. García-Ruano Synthesis 2001 2175 2179
-
(2001)
Synthesis
, pp. 2175-2179
-
-
Cañibano, V.1
Rodríguez, J.F.2
Santos, M.3
Sanz-Tejedor, M.A.4
Carreño, M.C.5
González, G.6
García-Ruano, J.L.7
-
35
-
-
71849087235
-
-
R. Fürst, I. Zupkó, Á. Berényi, G.F. Ecker, and U. Rinner Bioorg. Med. Chem. Lett. 19 2009 6948 6951
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 6948-6951
-
-
Fürst, R.1
Zupkó, I.2
Berényi, A.3
Ecker, G.F.4
Rinner, U.5
-
37
-
-
0031798378
-
-
Compound 6e was previously synthesized, using a Sonogashira coupling reaction between 3,4,5-trimethoxyphenylacetylene 8 and 2-iodo-thiophene
-
Compound 6e was previously synthesized, using a Sonogashira coupling reaction between 3,4,5-trimethoxyphenylacetylene 8 and 2-iodo-thiophene: J.A. Hadfield, and A.T. McGown Synth. Commun. 28 1998 1421 1431
-
(1998)
Synth. Commun.
, vol.28
, pp. 1421-1431
-
-
Hadfield, J.A.1
McGown, A.T.2
-
40
-
-
38349078209
-
-
A. Giraud, O. Provot, A. Hamzé, J.-D. Brion, and M. Alami Tetrahedron Lett. 49 2008 1107 1110
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 1107-1110
-
-
Giraud, A.1
Provot, O.2
Hamzé, A.3
Brion, J.-D.4
Alami, M.5
-
42
-
-
33745313891
-
-
3COOH in THF led to the complete degradation of the starting material 1c), according to this protocol
-
3COOH in THF led to the complete degradation of the starting material 1c), according to this protocol: M. Chakrabarty, T. Kundu, and Y. Harigaya Synth. Commun. 36 2006 2069 2077
-
(2006)
Synth. Commun.
, vol.36
, pp. 2069-2077
-
-
Chakrabarty, M.1
Kundu, T.2
Harigaya, Y.3
-
48
-
-
12144288301
-
-
M. Rosillo, G. Domínguez, L. Casarrubios, U. Amador, and J. Pérez-Castells J. Org. Chem. 69 2004 2084 2093
-
(2004)
J. Org. Chem.
, vol.69
, pp. 2084-2093
-
-
Rosillo, M.1
Domínguez, G.2
Casarrubios, L.3
Amador, U.4
Pérez-Castells, J.5
|