-
2
-
-
0000789168
-
-
and references cited therein.
-
D.H. Turner, N. Sugimoto, R. Hierzek and S.D. Dreiker, J. Am. Chem. Soc., 1987, 109, 3783, and references cited therein.
-
(1987)
J. Am. Chem. Soc.
, vol.109
, pp. 3783
-
-
Turner, D.H.1
Sugimoto, N.2
Hierzek, R.3
Dreiker, S.D.4
-
3
-
-
0025290381
-
-
and references cited therein.
-
J. RebekJr., Angew. Chem., Int. Ed. Eng., 1990, 29, 245, and references cited therein.
-
(1990)
Angew. Chem., Int. Ed. Eng.
, vol.29
, pp. 245
-
-
Rebek, J.1
-
5
-
-
0001064888
-
-
T.R. Kelly, C. Zhao and G.J. Bridger, J. Am. Chem. Soc., 1989, 111, 3744
-
(1989)
J. Am. Chem. Soc.
, vol.111
, pp. 3744
-
-
Kelly, T.R.1
Zhao, C.2
Bridger, G.J.3
-
6
-
-
33845279578
-
-
Y. Aoyama, Y. Tanaka, H. Toi and H. Ogoshi, J. Am. Chem. Soc., 1988, 110, 634
-
(1988)
J. Am. Chem. Soc.
, vol.110
, pp. 634
-
-
Aoyama, Y.1
Tanaka, Y.2
Toi, H.3
Ogoshi, H.4
-
7
-
-
37049083485
-
-
K. Kano, K. Yoshiyasu and S. Hashimoto, J. Chem. Soc., Chem. Commun., 1988, 801
-
(1988)
J. Chem. Soc., Chem. Commun.
, pp. 801
-
-
Kano, K.1
Yoshiyasu, K.2
Hashimoto, S.3
-
8
-
-
0001443927
-
-
G. Wulff, B. Heide and G. Helfmeier, J. Am. Chem. Soc., 1986, 108, 1089
-
(1986)
J. Am. Chem. Soc.
, vol.108
, pp. 1089
-
-
Wulff, G.1
Heide, B.2
Helfmeier, G.3
-
10
-
-
0023933033
-
-
However, a detailed examination on extraction species, stoichiometry and monolayer formations with lipophilic boronic acids has not been reported.Shinbo et al. reported on the transport of several saccharides with phenylboronic acid across a liquid membrane:
-
T. Shinbo, Maku (Membrane), 1988, 13, 153, However, a detailed examination on extraction species, stoichiometry and monolayer formations with lipophilic boronic acids has not been reported.Shinbo et al. reported on the transport of several saccharides with phenylboronic acid across a liquid membrane:
-
(1988)
Maku (Membrane)
, vol.13
, pp. 153
-
-
Shinbo, T.1
-
12
-
-
0001755537
-
-
The details of the peak assignment will be reported in a full manuscript.Kurihara et al. recently found that resorcinol–dodecanal cyclotetramer forms a stable monolayer at the air–water interface and recognizes sugar molecules:
-
K. Kurihara, K. Ohto, Y. Tanaka, Y. Aoyama and T. Kunitake, J. Am. Chem. Soc., 1991, 113, 444, The details of the peak assignment will be reported in a full manuscript.Kurihara et al. recently found that resorcinol–dodecanal cyclotetramer forms a stable monolayer at the air–water interface and recognizes sugar molecules:
-
(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 444
-
-
Kurihara, K.1
Ohto, K.2
Tanaka, Y.3
Aoyama, Y.4
Kunitake, T.5
|