-
1
-
-
0001213492
-
-
Chem. Rev
-
Recent reviews and publications: a) P. J. Stang and V. V. Zhdankin, Chem. Rev, 1996, 96, 1123;
-
(1996)
, vol.96
, pp. 1123
-
-
Stang, P.J.1
Zhdankin, V.V.2
-
2
-
-
0001382837
-
-
b) Y. Kita, T. Takada, and H. Tohma, Pure Appl. Chem., 1996, 68, 627;
-
(1996)
Pure Appl. Chem.
, vol.68
, pp. 627
-
-
Kita, Y.1
Takada, T.2
Tohma, H.3
-
5
-
-
79952768276
-
-
Hypervalent Iodine Chemistry; T. Wirth, Ed.; Springer-Verlag: Berlin, Heidelberg, 2003
-
e) Hypervalent Iodine Chemistry; T. Wirth, Ed.; Springer-Verlag: Berlin, Heidelberg, 2003;
-
-
-
-
9
-
-
0000565676
-
-
Our previous works for phenolic oxidations: a) Y. Tamura, T. Yakura, J. Haruta, and Y. Kita, J. Org. Chem, 1987, 52, 3927;
-
(1987)
J. Org. Chem
, vol.52
, pp. 3927
-
-
Tamura, Y.1
Yakura, T.2
Haruta, J.3
Kita, Y.4
-
10
-
-
0000179169
-
-
b) Y. Kita, H. Tohma, K. Kikuchi, M. Inagaki, and T. Yakura, J. Org. Chem, 1991, 56, 435;
-
(1991)
J. Org. Chem
, vol.56
, pp. 435
-
-
Kita, Y.1
Tohma, H.2
Kikuchi, K.3
Inagaki, M.4
Yakura, T.5
-
11
-
-
0026572391
-
-
c) Y. Kita, H. Tohma, M. Inagaki, K. Hatanaka, and T. Yakura, J. Am. Chem. Soc., 1992, 114, 2175;
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 2175
-
-
Kita, Y.1
Tohma, H.2
Inagaki, M.3
Hatanaka, K.4
Yakura, T.5
-
12
-
-
0000247985
-
-
d) Y. Kita, M. Arisawa, M. Gyoten, M. Nakajima, R. Hamada, H. Tohma, and T. Takada, J. Org. Chem, 1998, 63, 6625;
-
(1998)
J. Org. Chem
, vol.63
, pp. 6625
-
-
Kita, Y.1
Arisawa, M.2
Gyoten, M.3
Nakajima, M.4
Hamada, R.5
Tohma, H.6
Takada, T.7
-
13
-
-
4043131985
-
-
e) H. Tohma, Y. Harayama, M. Hashizume, M. Iwata, M. Egi, and Y. Kita, Angew. Chem, 2002, 114, 358;
-
(2002)
Angew. Chem
, vol.114
, pp. 358
-
-
Tohma, H.1
Harayama, Y.2
Hashizume, M.3
Iwata, M.4
Egi, M.5
Kita, Y.6
-
15
-
-
25844524611
-
-
f) T. Dohi, A. Maruyama, M. Yoshimura, K. Morimoto, H. Tohma, and Y. Kita, Angew. Chem. Int. Ed., 2005, 44, 6193;
-
(2005)
Angew. Chem. Int. Ed.
, vol.44
, pp. 6193
-
-
Dohi, T.1
Maruyama, A.2
Yoshimura, M.3
Morimoto, K.4
Tohma, H.5
Kita, Y.6
-
16
-
-
54049111473
-
-
g) T. Dohi, Y. Minamitsuji, A. Maruyama, S. Hirose, and Y. Kita, Org. Lett., 2008, 10, 3559;
-
(2008)
Org. Lett.
, vol.10
, pp. 3559
-
-
Dohi, T.1
Minamitsuji, Y.2
Maruyama, A.3
Hirose, S.4
Kita, Y.5
-
17
-
-
67949091066
-
-
h) Y. Minamitsuji, D. Kato, H. Fujioka, T. Dohi, and Y. Kita, Aust. J. Chem., 2009, 62, 648.
-
(2009)
Aust. J. Chem.
, vol.62
, pp. 648
-
-
Minamitsuji, Y.1
Kato, D.2
Fujioka, H.3
Dohi, T.4
Kita, Y.5
-
18
-
-
45549094716
-
-
a) T. Dohi, A. Maruyama, N. Takenaga, K. Senami, Y. Minamitsuji, H. Fujioka, S. B. Caemmerer, and Y. Kita, Angew. Chem. Int. Ed, 2008, 47, 3787;
-
(2008)
Angew. Chem. Int. Ed
, vol.47
, pp. 3787
-
-
Dohi, T.1
Maruyama, A.2
Takenaga, N.3
Senami, K.4
Minamitsuji, Y.5
Fujioka, H.6
Caemmerer, S.B.7
Kita, Y.8
-
20
-
-
0034597522
-
-
For recent reports of natural product syntheses containing the ortho-spirolactone structures, see: a) C. Cox and S. J. Danishefsky, Org. Lett., 2000, 2, 3493;
-
(2000)
Org. Lett.
, vol.2
, pp. 3493
-
-
Cox, C.1
Danishefsky, S.J.2
-
21
-
-
0345651549
-
-
b) T. Siu, C. D. Cox, and S. J. Danishefsky, Angew. Chem, 2003, 115, 5787;
-
(2003)
Angew. Chem
, vol.115
, pp. 5787
-
-
Siu, T.1
Cox, C.D.2
Danishefsky, S.J.3
-
22
-
-
0344792636
-
-
Angew. Chem. Int. Ed., 2003, 42, 5629
-
(2003)
, vol.42
, pp. 5629
-
-
Ed, Int.1
-
23
-
-
33645024479
-
-
c) D. A. Henderson, P. N. Collier, G. Pave, P. Rzepa, A. J. P. White, J. N. Burrows, and A. G. M. Barrett, J. Org. Chem, 2006, 71, 2434;
-
(2006)
J. Org. Chem
, vol.71
, pp. 2434
-
-
Henderson, D.A.1
Collier, P.N.2
Pave, G.3
Rzepa, P.4
White, A.J.P.5
Burrows, J.N.6
Barrett, A.G.M.7
-
24
-
-
33845936860
-
-
d) F. Konno, T. Ishikawa, M. Kawahata, and K. Yamaguchi, J. Org. Chem., 2006, 71, 9818.
-
(2006)
J. Org. Chem.
, vol.71
, pp. 9818
-
-
Konno, F.1
Ishikawa, T.2
Kawahata, M.3
Yamaguchi, K.4
-
25
-
-
37049107422
-
-
For previous report on the structure of 4, see: J. Gallos, A. Varvoglis, and N. W. Alcock, J. Chem. Soc., Perkin Trans. 1, 1985, 757.
-
(1985)
J. Chem. Soc., Perkin Trans.
, vol.1
, pp. 757
-
-
Gallos, J.1
Varvoglis, A.2
Alcock, N.W.3
-
26
-
-
0001677413
-
-
In contrast, the cyclohexa-2,4-dienones obtained from the oxidations of simple phenol carboxylic acids are generally quite reactive and have high propensity toward self-dimerization through the Diels-Alder process. For selected example, see: I. Drutu, J. T. Njardarson, and J. L. Wood, Org. Lett., 2002, 4, 493.
-
(2002)
Org. Lett.
, vol.4
, pp. 493
-
-
Drutu, I.1
Njardarson, J.T.2
Wood, J.L.3
-
29
-
-
0003683019
-
-
Tetrahedron Organic Chemistry Series, Pergamon, Oxford
-
c) Ligand Coupling Reaction with Het eroatomic Compounds, ed. Finet, P. Tetrahedron Organic Chemistry Series, Pergamon, Oxford, 1998, vol. 18.
-
(1998)
Ligand Coupling Reaction with Het Eroatomic Compounds
, vol.18
-
-
Finet, P.1
-
30
-
-
2342614837
-
-
J. Posakony, M. Hirao, S. Stevens, J. A. Simon, and A. Bedalov, J. Med. Chem., 2004, 47, 2635.
-
(2004)
J. Med. Chem.
, vol.47
, pp. 2635
-
-
Posakony, J.1
Hirao, M.2
Stevens, S.3
Simon, J.A.4
Bedalov, A.5
-
31
-
-
0036233741
-
-
Y. Kitani, A. Morita, T. Kumamoto, and T. Ishikawa, Helv. Chim. Acta, 2002, 85, 1186.
-
(2002)
Helv. Chim. Acta
, vol.85
, pp. 1186
-
-
Kitani, Y.1
Morita, A.2
Kumamoto, T.3
Ishikawa, T.4
|