-
1
-
-
33845908742
-
-
Kuboki A., Yamamoto T., Taira M., Arishige T., and Ohira S. Tetrahedron Lett. 48 (2007) 771-774
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 771-774
-
-
Kuboki, A.1
Yamamoto, T.2
Taira, M.3
Arishige, T.4
Ohira, S.5
-
2
-
-
40849145269
-
-
Kuboki A., Yamamoto T., Taira M., Arishige T., Konishi R., Hamabata M., Shirahama M., Hiramatsu T., Kuyama K., and Ohira S. Tetrahedron Lett. 49 (2008) 2558-2561
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 2558-2561
-
-
Kuboki, A.1
Yamamoto, T.2
Taira, M.3
Arishige, T.4
Konishi, R.5
Hamabata, M.6
Shirahama, M.7
Hiramatsu, T.8
Kuyama, K.9
Ohira, S.10
-
4
-
-
0001467212
-
-
Mizuno M., Kojima H., Tanaka T., Iinuma M., Kimura R., Min Z.D., and Murata H. Phytochemistry 26 (1987) 2071-2074
-
(1987)
Phytochemistry
, vol.26
, pp. 2071-2074
-
-
Mizuno, M.1
Kojima, H.2
Tanaka, T.3
Iinuma, M.4
Kimura, R.5
Min, Z.D.6
Murata, H.7
-
9
-
-
18744398777
-
-
Wu P.-L., Wu T.-S., He C.-X., Su C.-H., and Lee K.-H. Chem. Pharm. Bull. 53 (2005) 56-59
-
(2005)
Chem. Pharm. Bull.
, vol.53
, pp. 56-59
-
-
Wu, P.-L.1
Wu, T.-S.2
He, C.-X.3
Su, C.-H.4
Lee, K.-H.5
-
10
-
-
33947144611
-
-
Jin W.Y., Min B.S., Lee J.P., Thuong P.T., Lee H.-K., Song K., Seong Y.H., and Bae K. Arch. Pharm. Res. 30 (2007) 172-176
-
(2007)
Arch. Pharm. Res.
, vol.30
, pp. 172-176
-
-
Jin, W.Y.1
Min, B.S.2
Lee, J.P.3
Thuong, P.T.4
Lee, H.-K.5
Song, K.6
Seong, Y.H.7
Bae, K.8
-
11
-
-
0021984591
-
-
Ray A.B., Chattopadhyay S.K., Kumar S., Konno C., Kiso Y., and Hikino H. Tetrahedron 41 (1985) 209-214
-
(1985)
Tetrahedron
, vol.41
, pp. 209-214
-
-
Ray, A.B.1
Chattopadhyay, S.K.2
Kumar, S.3
Konno, C.4
Kiso, Y.5
Hikino, H.6
-
12
-
-
34249997599
-
-
Iizuka T., Nagumo E., Yotsumoto H., Moriyama H., and Nagai M. Biol. Pharm. Bull. 30 (2007) 1164-1166
-
(2007)
Biol. Pharm. Bull.
, vol.30
, pp. 1164-1166
-
-
Iizuka, T.1
Nagumo, E.2
Yotsumoto, H.3
Moriyama, H.4
Nagai, M.5
-
13
-
-
17444421649
-
-
Ahmad V.U., Ullah F., Hussain J., Farooq U., Zubair M., Khan M.T.H., and Choudhary M.I. Chem. Pharm. Bull. 52 (2004) 1458-1461
-
(2004)
Chem. Pharm. Bull.
, vol.52
, pp. 1458-1461
-
-
Ahmad, V.U.1
Ullah, F.2
Hussain, J.3
Farooq, U.4
Zubair, M.5
Khan, M.T.H.6
Choudhary, M.I.7
-
15
-
-
34147150245
-
-
Jin W.Y., Thuong P.T., Nguyen D., Min B.S., Son K.H., Chang H.W., Kim H.P., Kang S.S., Sok D.E., and Bae K. Arch. Pharm. Res. 30 (2007) 275-281
-
(2007)
Arch. Pharm. Res.
, vol.30
, pp. 275-281
-
-
Jin, W.Y.1
Thuong, P.T.2
Nguyen, D.3
Min, B.S.4
Son, K.H.5
Chang, H.W.6
Kim, H.P.7
Kang, S.S.8
Sok, D.E.9
Bae, K.10
-
24
-
-
0141631685
-
-
Ozanne A., Pouysegu L., Depernet D., François B., and Quideau S. Org. Lett. 5 (2003) 2903-2906
-
(2003)
Org. Lett.
, vol.5
, pp. 2903-2906
-
-
Ozanne, A.1
Pouysegu, L.2
Depernet, D.3
François, B.4
Quideau, S.5
-
25
-
-
44749094078
-
-
note
-
14{A figure is presented}
-
-
-
-
26
-
-
44749087274
-
-
note
-
Since cycloaddition of 6c with 2 did not proceed, the TBS substituent (6a) was used in the procedure.
-
-
-
-
27
-
-
44749087009
-
-
note
-
In a preliminary investigation, we found that the target o-quinone 20 was generated selectively in 59% yield from 19 with no substituent at C-6 of 6d. On the basis of this result, we initially planned the synthesis using 6d.{A figure is presented}
-
-
-
-
29
-
-
44749092465
-
-
note
-
5): δ 56.1, 56.3, 60.8, 77.9, 79.9, 101.0, 106.3, 111.9, 113.8, 126.4, 133.0, 138.4, 139.3, 144.4, 146.3, 149.2, 160.7.
-
-
-
|