-
1
-
-
0023618387
-
-
P.G. Baraldi, A. Barco, S. Benetti, G.P. Pollini, and D. Simoni Synthesis 1987 857 869
-
(1987)
Synthesis
, pp. 857-869
-
-
Baraldi, P.G.1
Barco, A.2
Benetti, S.3
Pollini, G.P.4
Simoni, D.5
-
2
-
-
17044424832
-
-
L. Martin, C. Polo, V. Ramos, T. Torroba, and S. Marcaccini Heterocycles 36 1993 2259 2265
-
(1993)
Heterocycles
, vol.36
, pp. 2259-2265
-
-
Martin, L.1
Polo, C.2
Ramos, V.3
Torroba, T.4
Marcaccini, S.5
-
3
-
-
0034092795
-
-
AMPA receptor antagonist: U. Madsen, F.A. Sløk, T.B. Stensbøl, H. Bräuner-Osborne, H.H. Lützhøft, M.V. Poulsen, L. Eriksen, and P. Krogsgaard-Larsen Eur. J. Med. Chem. 35 2000 69 76
-
(2000)
Eur. J. Med. Chem.
, vol.35
, pp. 69-76
-
-
Madsen, U.1
Sløk, F.A.2
Stensbøl, T.B.3
Bräuner-Osborne, H.4
Lützhøft, H.H.5
Poulsen, M.V.6
Eriksen, L.7
Krogsgaard-Larsen, P.8
-
4
-
-
0002219569
-
-
Antibacterial activity: Y.K. Kang, K.J. Shin, K.H. Yoo, K.J. Seo, C.Y. Hong, C. Lee, S.Y. Park, D.J. Kim, and S.W. Park Biorg. Med. Chem. Lett. 10 2000 95 99
-
(2000)
Biorg. Med. Chem. Lett.
, vol.10
, pp. 95-99
-
-
Kang, Y.K.1
Shin, K.J.2
Yoo, K.H.3
Seo, K.J.4
Hong, C.Y.5
Lee, C.6
Park, S.Y.7
Kim, D.J.8
Park, S.W.9
-
5
-
-
0032535501
-
-
Antiplatelet effect: C. Xue, J. Roderick, S. Mousa, R.E. Olson, and W.F. DeGrado Biorg. Med. Chem. Lett. 8 1998 3499 3504
-
(1998)
Biorg. Med. Chem. Lett.
, vol.8
, pp. 3499-3504
-
-
Xue, C.1
Roderick, J.2
Mousa, S.3
Olson, R.E.4
Degrado, W.F.5
-
6
-
-
0026697933
-
-
Anticonvulsant agents: (a) F. Lepage, F. Tombret, G. Cuvier, A. Marivain, and J.M. Gillardin Eur. J. Med. Chem. 27 1992 581 593
-
(1992)
Eur. J. Med. Chem.
, vol.27
, pp. 581-593
-
-
Lepage, F.1
Tombret, F.2
Cuvier, G.3
Marivain, A.4
Gillardin, J.M.5
-
7
-
-
0037205948
-
-
N.D. Eddintong, D.S. Cox, R.R. Roberts, R.J. Butcher, I.O. Edafiogho, J.P. Stables, N. Cooke, A.M. Goodwin, C.A. Smith, and K.R. Scott Eur. J. Med. Chem. 37 2002 635 648
-
(2002)
Eur. J. Med. Chem.
, vol.37
, pp. 635-648
-
-
Eddintong, N.D.1
Cox, D.S.2
Roberts, R.R.3
Butcher, R.J.4
Edafiogho, I.O.5
Stables, J.P.6
Cooke, N.7
Goodwin, A.M.8
Smith, C.A.9
Scott, K.R.10
-
9
-
-
0021883262
-
-
G.D. Diana, M.A. McKinlay, C.J. Brisson, E.S. Zalay, J.V. Miralles, and U.J. Salvador J. Med. Chem. 28 1985 748 752
-
(1985)
J. Med. Chem.
, vol.28
, pp. 748-752
-
-
Diana, G.D.1
McKinlay, M.A.2
Brisson, C.J.3
Zalay, E.S.4
Miralles, J.V.5
Salvador, U.J.6
-
10
-
-
0032311436
-
-
Immunostimulatory activity: S. Ryng, Z. Machoń, Z. Wieczorek, M. Zimecki, and M. Mokrosz Eur. J. Med. Chem. 33 1998 831 836
-
(1998)
Eur. J. Med. Chem.
, vol.33
, pp. 831-836
-
-
Ryng, S.1
MacHoń, Z.2
Wieczorek, Z.3
Zimecki, M.4
Mokrosz, M.5
-
11
-
-
17044412371
-
-
Fr Patent No. 1526466;
-
Fr Patent No. 1526466; Chem. Abstr. 1968, 71, 61373.
-
(1968)
Chem. Abstr.
, vol.71
, pp. 61373
-
-
-
12
-
-
85030793954
-
-
US Patent No. 512961;
-
Auinbauh, S. M.; Lee, L. F.; McDermott, L. L. US Patent No. 512961; Chem. Abstr. 1992, 117, 171434.
-
(1992)
Chem. Abstr.
, vol.117
, pp. 171434
-
-
Auinbauh, S.M.1
Lee, L.F.2
McDermott, L.L.3
-
13
-
-
17044409521
-
-
RU Pat. No. 2088229-C1;
-
Demina, O. V.; Varfolomeev, S. D.; Vzheshch, P. V.; Tatarintsev, A. V. RU Pat. No. 2088229-C1; Chem. Abstr. 1998, 128, 43855.
-
(1998)
Chem. Abstr.
, vol.128
, pp. 43855
-
-
Demina, O.V.1
Varfolomeev, S.D.2
Vzheshch, P.V.3
Tatarintsev, A.V.4
-
14
-
-
85030798125
-
-
US Patent No. 2003 114491;
-
Kim, Y.; Kang, S. B.; Keum, G.; Jang, M. S.; Kong, J. Y.; Jeong, D. Y. US Patent No. 2003 114491; Chem. Abstr. 2003, 139, 53009.
-
(2003)
Chem. Abstr.
, vol.139
, pp. 53009
-
-
Kim, Y.1
Kang, S.B.2
Keum, G.3
Jang, M.S.4
Kong, J.Y.5
Jeong, D.Y.6
-
15
-
-
17044388832
-
-
RU Patent No. 2196772;
-
Vasilin, V. K.; Kajgorodova, E. A.; Krapivin, G. D.; Nen'ko, N. I.; Fedjun, E. V. RU Patent No. 2196772; Chem. Abstr. 2003, 139, 395921.
-
(2003)
Chem. Abstr.
, vol.139
, pp. 395921
-
-
Vasilin, V.K.1
Kajgorodova, E.A.2
Krapivin, G.D.3
Nen'ko, N.I.4
Fedjun, E.V.5
-
16
-
-
0002715136
-
-
F. Fariña, M.T. Fraile, M.R. Martín, M.V. Martín, and A. Martínez Heterocycles 40 1995 285 292
-
(1995)
Heterocycles
, vol.40
, pp. 285-292
-
-
Fariña, F.1
Fraile, M.T.2
Martín, M.R.3
Martín, M.V.4
Martínez, A.5
-
18
-
-
0003153666
-
-
E. Belgodere, R. Bossio, F. De Sio, S. Marcaccini, and R. Pepino Heterocycles 20 1983 501 504
-
(1983)
Heterocycles
, vol.20
, pp. 501-504
-
-
Belgodere, E.1
Bossio, R.2
De Sio, F.3
Marcaccini, S.4
Pepino, R.5
-
21
-
-
85030799218
-
-
note
-
The dipolarophile 7 was obtained from methyl bromoacetate following the procedure reported by us in reference 14 for the preparation of racemic compound 3.
-
-
-
-
22
-
-
85030802713
-
-
note
-
13C NMR spectra for compounds 6A and 8A could not be recorded due to their low proportion in the reaction mixture.
-
-
-
-
23
-
-
0000719372
-
-
P. Caramella, E. Albini, T. Bandiera, A.C. Coda, P. Grünanger, and F.M. Albini Tetrahedron 39 1983 689 699
-
(1983)
Tetrahedron
, vol.39
, pp. 689-699
-
-
Caramella, P.1
Albini, E.2
Bandiera, T.3
Coda, A.C.4
Grünanger, P.5
Albini, F.M.6
-
24
-
-
0003178971
-
-
M. Barzaghi, P.L. Beltrame, P. Dalla, P. Del Buttero, E. Licandro, S. Maiorana, and G. Zecchi J. Org. Chem. 48 1983 3807 3810
-
(1983)
J. Org. Chem.
, vol.48
, pp. 3807-3810
-
-
Barzaghi, M.1
Beltrame, P.L.2
Dalla, P.3
Del Buttero, P.4
Licandro, E.5
Maiorana, S.6
Zecchi, G.7
-
26
-
-
2742594847
-
-
P. Bravo, L. Bruché, M. Crucianelli, A. Farina, S.V. Meille, A. Merli, and P. Seresini J. Chem. Res. (S) 1996 348 349
-
(1996)
J. Chem. Res. (S)
, pp. 348-349
-
-
Bravo, P.1
Bruché, L.2
Crucianelli, M.3
Farina, A.4
Meille, S.V.5
Merli, A.6
Seresini, P.7
-
27
-
-
1542405044
-
-
P. Bravo, L. Bruché, M. Crucianelli, A. Farina, S.V. Meille, A. Merli, and P. Seresini J. Chem. Res. (M) 1996 1901 1923
-
(1996)
J. Chem. Res. (M)
, pp. 1901-1923
-
-
Bravo, P.1
Bruché, L.2
Crucianelli, M.3
Farina, A.4
Meille, S.V.5
Merli, A.6
Seresini, P.7
-
29
-
-
85030796271
-
-
Patent No. WO 2003013517;
-
Cavicchioli, M.; Pevarello, P.; Salom, B.; Vulpetti, A. Patent No. WO 2003013517; Chem. Abstr. 2003, 138, 187773.
-
(2003)
Chem. Abstr.
, vol.138
, pp. 187773
-
-
Cavicchioli, M.1
Pevarello, P.2
Salom, B.3
Vulpetti, A.4
-
31
-
-
0034608622
-
-
T. Owa, T. Okauchi, K. Yoshimatsu, N.H. Sugi, Y. Ozawa, T. Nagasu, N. Koyanagi, T. Okabe, K. Kitoh, and H. Yoshino Biorg. Med. Chem. Lett. 10 2000 1223 1226 and references therein cited
-
(2000)
Biorg. Med. Chem. Lett.
, vol.10
, pp. 1223-1226
-
-
Owa, T.1
Okauchi, T.2
Yoshimatsu, K.3
Sugi, N.H.4
Ozawa, Y.5
Nagasu, T.6
Koyanagi, N.7
Okabe, T.8
Kitoh, K.9
Yoshino, H.10
-
32
-
-
85030805474
-
-
note
-
Formolysis of acetal group in the 4-(diethoxymethyl)-3-pyridin-3- ylisoxazol-5-carboxamides followed by reductive amination also afforded the corresponding amide-amines in good yields, personal communication.
-
-
-
-
34
-
-
0141856847
-
-
PCUS5633272;
-
Talley, J. J.; Brown, D. L.; Nagarajan, S.; Carter, J. S.; Weier, R. M.; Stealey, M. A.; Colins, P. W.; Rogers, R. S.; Seibert, K. PCUS5633272; Chem. Abstr. 1997, 127, 65756.
-
(1997)
Chem. Abstr.
, vol.127
, pp. 65756
-
-
Talley, J.J.1
Brown, D.L.2
Nagarajan, S.3
Carter, J.S.4
Weier, R.M.5
Stealey, M.A.6
Colins, P.W.7
Rogers, R.S.8
Seibert, K.9
-
35
-
-
85030798717
-
-
PC US 2004176407;
-
Nakamura, M.; Kurihara, H.; Ohkubo, M.; Tsukamoto, N. PC US 2004176407; Chem. Abstr. 2004, 141, 243542.
-
(2004)
Chem. Abstr.
, vol.141
, pp. 243542
-
-
Nakamura, M.1
Kurihara, H.2
Ohkubo, M.3
Tsukamoto, N.4
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