-
3
-
-
0028576943
-
-
Wells P. S., Holbrook A. M., Crowther N. R., Hirsh J., Ann. Intern. Med., 121, 676-683 (1994).
-
(1994)
Ann. Intern. Med
, vol.121
, pp. 676-683
-
-
Wells, P.S.1
Holbrook, A.M.2
Crowther, N.R.3
Hirsh, J.4
-
5
-
-
0029111442
-
-
Hara T., Yokoyama A., Tanabe K., Ishihara H., Iwamoto M., Thromb. Haemost., 1995, 635-639 (1995).
-
(1995)
Thromb. Haemost
, vol.1995
, pp. 635-639
-
-
Hara, T.1
Yokoyama, A.2
Tanabe, K.3
Ishihara, H.4
Iwamoto, M.5
-
6
-
-
0031793092
-
-
Sato K., Taniuchi Y., Kawasaki T., Hirayama F., Koshio H., Matsumoto Y., Iizumi Y., Jpn. J. Pharmacol., 1998, 191-197 (1998).
-
(1998)
Jpn. J. Pharmacol
, vol.1998
, pp. 191-197
-
-
Sato, K.1
Taniuchi, Y.2
Kawasaki, T.3
Hirayama, F.4
Koshio, H.5
Matsumoto, Y.6
Iizumi, Y.7
-
7
-
-
32044457418
-
-
Noguchi T., Tanaka N., Nishimata T., Goto R., Hayakawa M., Sugidachi A., Ogawa T., Asai F., Matsui Y., Fujimoto K., Chem. Pharm. Bull., 54, 163-174 (2006).
-
(2006)
Chem. Pharm. Bull
, vol.54
, pp. 163-174
-
-
Noguchi, T.1
Tanaka, N.2
Nishimata, T.3
Goto, R.4
Hayakawa, M.5
Sugidachi, A.6
Ogawa, T.7
Asai, F.8
Matsui, Y.9
Fujimoto, K.10
-
8
-
-
0027536014
-
-
Tsunoda T., Yamamiya Y., Ito S., Tetrahedron Lett., 34, 1639-1642 (1993).
-
(1993)
Tetrahedron Lett
, vol.34
, pp. 1639-1642
-
-
Tsunoda, T.1
Yamamiya, Y.2
Ito, S.3
-
10
-
-
0029803790
-
-
Judkins B. D., Allen D. G., Cook T. A., Evans B., Sardharwala T. E., Synth. Commum., 26, 4351-4367 (1996).
-
(1996)
Synth. Commum
, vol.26
, pp. 4351-4367
-
-
Judkins, B.D.1
Allen, D.G.2
Cook, T.A.3
Evans, B.4
Sardharwala, T.E.5
-
11
-
-
34047124612
-
-
1H-NMR spectra.
-
1H-NMR spectra.
-
-
-
-
12
-
-
33845373480
-
-
Bartori G., Bosco M., Dalpozzo R., Todesco E. P., J. Org. Chem., 51, 3694-3696 (1986).
-
(1986)
J. Org. Chem
, vol.51
, pp. 3694-3696
-
-
Bartori, G.1
Bosco, M.2
Dalpozzo, R.3
Todesco, E.P.4
-
13
-
-
0037330363
-
-
Huang W., Zhang P., Zuckett J. F., Wang L., Woolfrey J., Song Y., Jia Z. J., Clizbe L. A., Su T., Tran K., Huang B., Wong P., Sinha U., Park G., Reed A., Malinowski J., Hollenbach S. J., Scarborough R. M., Zhu B., Bioorg. Med. Chem. Lett., 13, 561-566 (2003).
-
(2003)
Bioorg. Med. Chem. Lett
, vol.13
, pp. 561-566
-
-
Huang, W.1
Zhang, P.2
Zuckett, J.F.3
Wang, L.4
Woolfrey, J.5
Song, Y.6
Jia, Z.J.7
Clizbe, L.A.8
Su, T.9
Tran, K.10
Huang, B.11
Wong, P.12
Sinha, U.13
Park, G.14
Reed, A.15
Malinowski, J.16
Hollenbach, S.J.17
Scarborough, R.M.18
Zhu, B.19
-
15
-
-
33751385493
-
-
Oh-e T., Miyaura N., Suzuki A., J. Org. Chem., 58, 2201-2208 (1993).
-
(1993)
J. Org. Chem
, vol.58
, pp. 2201-2208
-
-
Oh-e, T.1
Miyaura, N.2
Suzuki, A.3
-
16
-
-
0035815138
-
-
Vice S., Bara T., Bauer A., Evans C. A., Ford J., Josien H., McCombie S., Miller M., Nazareno D., Palani A., Tagat J., J. Org. Chem., 66, 2487-2492 (2001).
-
(2001)
J. Org. Chem
, vol.66
, pp. 2487-2492
-
-
Vice, S.1
Bara, T.2
Bauer, A.3
Evans, C.A.4
Ford, J.5
Josien, H.6
McCombie, S.7
Miller, M.8
Nazareno, D.9
Palani, A.10
Tagat, J.11
-
17
-
-
13944261905
-
-
Ting P. C., Lee J. F., Wu J., Umland S. P., Aslanian R., Cao J., Dong Y., Garlisi C. G., Gilbert E. J., Huang Y., Jakway J., Kelly J., Liu Z., McCombie S., Shah H., Tian F., Wan Y., Shih N.-Y., Bioorg. Med. Chem. Lett., 15, 1375-1378 (2005).
-
(2005)
Bioorg. Med. Chem. Lett
, vol.15
, pp. 1375-1378
-
-
Ting, P.C.1
Lee, J.F.2
Wu, J.3
Umland, S.P.4
Aslanian, R.5
Cao, J.6
Dong, Y.7
Garlisi, C.G.8
Gilbert, E.J.9
Huang, Y.10
Jakway, J.11
Kelly, J.12
Liu, Z.13
McCombie, S.14
Shah, H.15
Tian, F.16
Wan, Y.17
Shih, N.-Y.18
-
18
-
-
34047126725
-
-
At first, we tried to adopt aryl amino reaction against trifluoromethanesulfonate 24 to prepare methylaminoindoline derivative 33.24,25 In spite of many efforts, the reaction was result in recovery of compound 24
-
24,25) In spite of many efforts, the reaction was result in recovery of compound 24.
-
-
-
-
19
-
-
1242308383
-
-
Han F., Hayashi M., Watanabe Y., Eur. J. Org. Chem., 2004, 558-566 (2004).
-
(2004)
Eur. J. Org. Chem
, vol.2004
, pp. 558-566
-
-
Han, F.1
Hayashi, M.2
Watanabe, Y.3
-
20
-
-
34047128489
-
-
In the previous report, S-3 was obtained from separation of (RS)-3 by preparative chiral HPLC, S)-3 was converted to compound (R)-35, then we determined the stereochemistry of (R)-35 and (S)-3 (the starting material of (R)-35) by X-ray crystallographic analysis of (R)-35. This time, each retention time of (S)-3 and (R)-3 was already in hand, so we determined their stereochemistry by comparison of its retention time, Chemical Equation Presented
-
In the previous report, (S)-3 was obtained from separation of (RS)-3 by preparative chiral HPLC. (S)-3 was converted to compound (R)-35, then we determined the stereochemistry of (R)-35 and (S)-3 (the starting material of (R)-35) by X-ray crystallographic analysis of (R)-35. This time, each retention time of (S)-3 and (R)-3 was already in hand, so we determined their stereochemistry by comparison of its retention time. (Chemical Equation Presented)
-
-
-
-
22
-
-
34047102764
-
-
max (10 min) was 7.0 mg/ml. As a result, no significant difference was observed in plasma concentration of both compounds. This result indicates that the difference of toxicity between (RS)-1 and 11d isn't induced by the plasma concentration but these compounds themselves (unpublished data).
-
max (10 min) was 7.0 mg/ml. As a result, no significant difference was observed in plasma concentration of both compounds. This result indicates that the difference of toxicity between (RS)-1 and 11d isn't induced by the plasma concentration but these compounds themselves (unpublished data).
-
-
-
-
23
-
-
33748621833
-
-
Guram A. F., Rennels R. A., Buchwald S. L., Angew. Chem. Int. Ed. Engl., 1995, 1348-1350 (1995).
-
(1995)
Angew. Chem. Int. Ed. Engl
, vol.1995
, pp. 1348-1350
-
-
Guram, A.F.1
Rennels, R.A.2
Buchwald, S.L.3
|