-
3
-
-
0033533863
-
-
M. Amblard, I. Daffix, P. Bedos, G. Bergé, D. Pruneau, J.-L. Paquet, J.-M. Luccarini, P. Bélichard, P. Dodey, and J. Martinez J. Med. Chem. 42 1999 4185 4192
-
(1999)
J. Med. Chem.
, vol.42
, pp. 4185-4192
-
-
Amblard, M.1
Daffix, I.2
Bedos, P.3
Bergé, G.4
Pruneau, D.5
Paquet, J.-L.6
Luccarini, J.-M.7
Bélichard, P.8
Dodey, P.9
Martinez, J.10
-
4
-
-
0035935705
-
-
P. Huang, G.H. Loew, H. Funamizu, M. Mimura, N. Ishiyama, M. Hayashida, T. Okuno, O. Shimada, A. Okuyama, S. Ikegami, J. Nakano, and K. Inoguchi J. Med. Chem. 44 2001 4082 4091
-
(2001)
J. Med. Chem.
, vol.44
, pp. 4082-4091
-
-
Huang, P.1
Loew, G.H.2
Funamizu, H.3
Mimura, M.4
Ishiyama, N.5
Hayashida, M.6
Okuno, T.7
Shimada, O.8
Okuyama, A.9
Ikegami, S.10
Nakano, J.11
Inoguchi, K.12
-
5
-
-
17944369560
-
-
D. Lesuisse, P. Deprez, E. Albert, T.T. Duc, B. Sortais, D. Gofflo, V. Jean-Baptiste, J.-P. Marquette, B. Schoot, E. Sarubbi, G. Lange, P. Broto, and E. Mandine Bioorg. Med. Chem. Lett. 11 2001 2127 2131
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 2127-2131
-
-
Lesuisse, D.1
Deprez, P.2
Albert, E.3
Duc, T.T.4
Sortais, B.5
Gofflo, D.6
Jean-Baptiste, V.7
Marquette, J.-P.8
Schoot, B.9
Sarubbi, E.10
Lange, G.11
Broto, P.12
Mandine, E.13
-
6
-
-
0025274987
-
-
H. Narita, M. Gaino, T. Suzuki, H. Kurosawa, H. Inoue, and T. Nagao Chem. Pharm. Bull. 38 1990 407 410
-
(1990)
Chem. Pharm. Bull.
, vol.38
, pp. 407-410
-
-
Narita, H.1
Gaino, M.2
Suzuki, T.3
Kurosawa, H.4
Inoue, H.5
Nagao, T.6
-
7
-
-
26844467504
-
-
U.S. Patent 5,770,594, 1998.
-
Hamanaka, E. S.; Hayward, C. M.; Hawkins, J. M. U.S. Patent 5,770,594, 1998.
-
-
-
Hamanaka, E.S.1
Hayward, C.M.2
Hawkins, J.M.3
-
8
-
-
4243307379
-
-
Chem. Abstr. 125 1996 168038s
-
(1996)
Chem. Abstr.
, vol.125
-
-
-
9
-
-
0000358111
-
-
J. Szabó, L. Fodor, Á Katócs, G. Bernáth, and P. Sohár Chem. Ber. 119 1986 2904 2913
-
(1986)
Chem. Ber.
, vol.119
, pp. 2904-2913
-
-
Szabó, J.1
Fodor, L.2
Katócs, Á.3
Bernáth, G.4
Sohár, P.5
-
11
-
-
0042744938
-
-
C. Faggi, M. García-Valverde, S. Marcaccini, R. Pepino, and M.C. Pozo Synthesis 2003 1553 1558
-
(2003)
Synthesis
, pp. 1553-1558
-
-
Faggi, C.1
García-Valverde, M.2
Marcaccini, S.3
Pepino, R.4
Pozo, M.C.5
-
12
-
-
26844485707
-
-
S. Marcaccini, R. Pepino, M.C. Pozo, S. Basurto, M. García- Valverde, and T. Torroba Tetrahedron Lett. 44 2003 3999 4001
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 3999-4001
-
-
Marcaccini, S.1
Pepino, R.2
Pozo, M.C.3
Basurto, S.4
García-Valverde, M.5
Torroba, T.6
-
14
-
-
0037247907
-
-
C.F. Marcos, S. Marcaccini, R. Pepino, C. Polo, and T. Torroba Synthesis 2003 691
-
(2003)
Synthesis
, pp. 691
-
-
Marcos, C.F.1
Marcaccini, S.2
Pepino, R.3
Polo, C.4
Torroba, T.5
-
18
-
-
26844548192
-
-
note
-
5 (516.37): C, 58.15; H, 4.49; N, 8.14. Found: C, 58.37; H, 4.60; N, 7.86. Detailed experimental procedures, physical, analytical, and spectral data of compounds 7b-k are reported in the Supplementary data.
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19
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26844439421
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note
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5S (477.53): C, 62.88; H, 4.85; N, 8.80. Found: C, 62.61; H, 4.96; N, 8.99. Detailed experimental procedures, physical, analytical, and spectral data of compounds 9b-k are reported in the Supplementary data.
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20
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0035939470
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The formation of the internal nucleophile represents the key step in this synthesis. From this point of view the present methodology is substantially analogous to those described by Hulme and Zhu groups: P. Tempest, V. Ma, M.G. Kelly, W. Jones, and C. Hulme Tetrahedron Lett. 42 2001 4963 4966
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 4963-4966
-
-
Tempest, P.1
Ma, V.2
Kelly, M.G.3
Jones, W.4
Hulme, C.5
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