-
1
-
-
0025041156
-
-
For example: A. Osuka, K. Maruyama, N. Mataga, T. Asahi, I. Yamazaki, and N. Tamai, J. Am. Chem. Soc., 112, 4958 (1990); J. L. Sessler, M. R. Johnson, S. E. Creager, J. C. Fettinger, and J. A. Ibers, J. Am. Chem. Soc., 112, 9310 (1990); A. Helms, D. Heiler, and G. McLendon, J. Am. Chem. Soc., 114, 6227 (1992).
-
(1990)
J. Am. Chem. Soc.
, vol.112
, pp. 4958
-
-
Osuka, A.1
Maruyama, K.2
Mataga, N.3
Asahi, T.4
Yamazaki, I.5
Tamai, N.6
-
2
-
-
0025694679
-
-
For example: A. Osuka, K. Maruyama, N. Mataga, T. Asahi, I. Yamazaki, and N. Tamai, J. Am. Chem. Soc., 112, 4958 (1990); J. L. Sessler, M. R. Johnson, S. E. Creager, J. C. Fettinger, and J. A. Ibers, J. Am. Chem. Soc., 112, 9310 (1990); A. Helms, D. Heiler, and G. McLendon, J. Am. Chem. Soc., 114, 6227 (1992).
-
(1990)
J. Am. Chem. Soc.
, vol.112
, pp. 9310
-
-
Sessler, J.L.1
Johnson, M.R.2
Creager, S.E.3
Fettinger, J.C.4
Ibers, J.A.5
-
3
-
-
2742545120
-
-
For example: A. Osuka, K. Maruyama, N. Mataga, T. Asahi, I. Yamazaki, and N. Tamai, J. Am. Chem. Soc., 112, 4958 (1990); J. L. Sessler, M. R. Johnson, S. E. Creager, J. C. Fettinger, and J. A. Ibers, J. Am. Chem. Soc., 112, 9310 (1990); A. Helms, D. Heiler, and G. McLendon, J. Am. Chem. Soc., 114, 6227 (1992).
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 6227
-
-
Helms, A.1
Heiler, D.2
McLendon, G.3
-
5
-
-
0029637583
-
-
G. McDermott, S. M. Prince, A. A. Freer, A. M. Hawthornthwaite-Lawless, M. Z. Papiz, R. J. Cogdell, and N. W. Isaacs, Nature, 374, 517 (1995).
-
(1995)
Nature
, vol.374
, pp. 517
-
-
McDermott, G.1
Prince, S.M.2
Freer, A.A.3
Hawthornthwaite-Lawless, A.M.4
Papiz, M.Z.5
Cogdell, R.J.6
Isaacs, N.W.7
-
6
-
-
0346655990
-
-
Y. Kobuke and H. Miyaji, J. Am. Chem. Soc., 116, 4111 (1994); C. M. Drain, K. C. Russell, and J.-M. Lehn, Chem. Commun., 1996, 337.
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 4111
-
-
Kobuke, Y.1
Miyaji, H.2
-
7
-
-
0039070397
-
-
Y. Kobuke and H. Miyaji, J. Am. Chem. Soc., 116, 4111 (1994); C. M. Drain, K. C. Russell, and J.-M. Lehn, Chem. Commun., 1996, 337.
-
Chem. Commun.
, vol.1996
, pp. 337
-
-
Drain, C.M.1
Russell, K.C.2
Lehn, J.-M.3
-
8
-
-
0001661713
-
-
For chiral diporphyrins, see: a) H. Tamiaki, S. Suzuki, and K. Maruyama, Bull. Chem. Soc. Jpn., 66, 2633 (1993).
-
(1993)
Bull. Chem. Soc. Jpn.
, vol.66
, pp. 2633
-
-
Tamiaki, H.1
Suzuki, S.2
Maruyama, K.3
-
9
-
-
37049079822
-
-
b) A. Vidal-Ferran, C. M. Müller, and J. K. M. Sanders, J. Chem. Soc., Chem. Commun., 1994, 2657.
-
J. Chem. Soc., Chem. Commun.
, vol.1994
, pp. 2657
-
-
Vidal-Ferran, A.1
Müller, C.M.2
Sanders, J.K.M.3
-
10
-
-
37049087101
-
-
c) M. J. Crossley, T. W. Hambley, L. G. Mackay, A. C. Try, and R. Walton, J. Chem. Soc., Chem. Commun., 1995, 1077.
-
J. Chem. Soc., Chem. Commun.
, vol.1995
, pp. 1077
-
-
Crossley, M.J.1
Hambley, T.W.2
Mackay, L.G.3
Try, A.C.4
Walton, R.5
-
11
-
-
85047671875
-
-
d) T. Ema, S. Nemugaki, S. Tsuboi, and M. Utaka, Tetrahedron Lett., 36, 5905 (1995).
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 5905
-
-
Ema, T.1
Nemugaki, S.2
Tsuboi, S.3
Utaka, M.4
-
12
-
-
0029999237
-
-
e) S. Matile, N. Berova, K. Nakanishi, J. Fleischhauer, and R. W. Woody, J. Am. Chem. Soc., 118, 5198 (1996).
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 5198
-
-
Matile, S.1
Berova, N.2
Nakanishi, K.3
Fleischhauer, J.4
Woody, R.W.5
-
13
-
-
1542530919
-
-
f) M. Takeuchi, Y. Chin, T. Imada, and S. Shinkai, Chem. Commun., 1996, 1867.
-
Chem. Commun.
, vol.1996
, pp. 1867
-
-
Takeuchi, M.1
Chin, Y.2
Imada, T.3
Shinkai, S.4
-
14
-
-
16244416275
-
-
g) H. Mihara, Y. Haruta, S. Sakamoto, N. Nishino, and H. Aoyagi, Chem. Lett., 1996, 1.
-
Chem. Lett.
, vol.1996
, pp. 1
-
-
Mihara, H.1
Haruta, Y.2
Sakamoto, S.3
Nishino, N.4
Aoyagi, H.5
-
15
-
-
84980295066
-
-
R. G. Little, J. A. Anton, P. A. Loach, and J. A. Ibers, J. Heterocyclic Chem., 12, 343 (1975).
-
(1975)
J. Heterocyclic Chem.
, vol.12
, pp. 343
-
-
Little, R.G.1
Anton, J.A.2
Loach, P.A.3
Ibers, J.A.4
-
16
-
-
0040938576
-
-
note
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The MM2 force field with augmented parameters implemented in the CAChe system (ver. 3.8, Sony /Tektronix) was used. The sequential search was adopted for the four dihedral angles in the cyclophane moiety. Each structure obtained was further optimized with the above dihedral angles unrestrained to yield several stable conformers.
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-
-
-
18
-
-
33645931591
-
-
I. Tabushi, S. Kugimiya, M. G. Kinnaird, and T. Sasaki, J. Am. Chem. Soc., 107, 4192 (1985).
-
(1985)
J. Am. Chem. Soc.
, vol.107
, pp. 4192
-
-
Tabushi, I.1
Kugimiya, S.2
Kinnaird, M.G.3
Sasaki, T.4
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