-
1
-
-
33846561914
-
-
Koshland, D. E., Jr. Proc. Natl. Acad. Sci. U.S.A. 1958, 44, 98-104.
-
(a) Koshland, D. E., Jr. Proc. Natl. Acad. Sci. U.S.A. 1958, 44, 98-104.
-
-
-
-
2
-
-
0031750973
-
-
Jr
-
(b) Koshland, D. E., Jr. Nature Med. 1998, 4, 1112-1114.
-
(1998)
Nature Med
, vol.4
, pp. 1112-1114
-
-
Koshland, D.E.1
-
4
-
-
0004178481
-
-
Hervé, G, Ed, CRC Press: Boca Raton, FL
-
(b) Hervé, G., Ed. Allosteric Enzymes; CRC Press: Boca Raton, FL, 1989.
-
(1989)
Allosteric Enzymes
-
-
-
6
-
-
4344577604
-
-
For some recent examples of synthetic allosteric catalysts, see: a, and references therein
-
For some recent examples of synthetic allosteric catalysts, see: (a) Kovbasyuk, L.; Krämer, R. Chem. Rev. 2004, 104, 3161-3188 and references therein,
-
(2004)
Chem. Rev
, vol.104
, pp. 3161-3188
-
-
Kovbasyuk, L.1
Krämer, R.2
-
7
-
-
33646530803
-
-
(b) Zhu, L; Anslyn, E. V. Angew. Chem., Int. Ed. 2006, 45, 1190-1196.
-
(2006)
Angew. Chem., Int. Ed
, vol.45
, pp. 1190-1196
-
-
Zhu, L.1
Anslyn, E.V.2
-
8
-
-
0034665212
-
-
(c) Fritsky, I. O.; Ott, R.; Krämer, R. Angew. Chem., Int. Ed. 2000, 39, 3255-3258.
-
(2000)
Angew. Chem., Int. Ed
, vol.39
, pp. 3255-3258
-
-
Fritsky, I.O.1
Ott, R.2
Krämer, R.3
-
9
-
-
0037029915
-
-
(d) Tozawa, T.; Tokita, S.; Kubo, Y. Tetrahedron Lett. 2002, 43, 3455-3457.
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 3455-3457
-
-
Tozawa, T.1
Tokita, S.2
Kubo, Y.3
-
10
-
-
0037117571
-
-
(e) Scarso, A.; Scheffer, S. U.; Gobel, M.; Broxterman, Q. B.; Kaptein, B.; Formaggio, F.; Toniolo, C.; Scrimin, P. Proc. Natl. Acad. Sci. U.S.A. 2002, 99, 5144-4149.
-
(2002)
Proc. Natl. Acad. Sci. U.S.A
, vol.99
, pp. 5144-4149
-
-
Scarso, A.1
Scheffer, S.U.2
Gobel, M.3
Broxterman, Q.B.4
Kaptein, B.5
Formaggio, F.6
Toniolo, C.7
Scrimin, P.8
-
11
-
-
0042355723
-
-
(f) Gianneschi, N. C.; Bertin, P. A.; Nguyen, S. T.; Mirkin, C. A.; Zakharov, L. N.; Rheingold, A. L. J. Am. Chem. Soc. 2003, 125, 10508-10509.
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 10508-10509
-
-
Gianneschi, N.C.1
Bertin, P.A.2
Nguyen, S.T.3
Mirkin, C.A.4
Zakharov, L.N.5
Rheingold, A.L.6
-
12
-
-
8444229360
-
-
(g) Gianneschi, N. C.; Cho, S.-H.; Nguyen, S. T.; Mirkin, C. A. Angew. Chem., Int. Ed. 2004, 43, 5503-5507.
-
(2004)
Angew. Chem., Int. Ed
, vol.43
, pp. 5503-5507
-
-
Gianneschi, N.C.1
Cho, S.-H.2
Nguyen, S.T.3
Mirkin, C.A.4
-
13
-
-
1442300790
-
-
(h) Takebayashi, S.; Ikeda, M.; Takeuchi, M.; Shinkai, S. Chem. Commun. 2004, 420-421.
-
(2004)
Chem. Commun
, pp. 420-421
-
-
Takebayashi, S.1
Ikeda, M.2
Takeuchi, M.3
Shinkai, S.4
-
14
-
-
13644252169
-
-
(i) Gianneschi, N. C.; Nguyen, S. T.; Mirkin, C. A. J. Am. Chem. Soc. 2005, 127, 1644-1645.
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 1644-1645
-
-
Gianneschi, N.C.1
Nguyen, S.T.2
Mirkin, C.A.3
-
15
-
-
0542421525
-
-
For several recent reviews, see: a
-
For several recent reviews, see: (a) Gellman, S. H. Acc. Chem. Res. 1998, 31, 173-180.
-
(1998)
Acc. Chem. Res
, vol.31
, pp. 173-180
-
-
Gellman, S.H.1
-
16
-
-
2142742534
-
-
(b) Kirshenbaum, K.; Zuckermann, R. N.; Dill, K. A. Curr. Opin. Struct. Biol. 1999, 9, 530-535.
-
(1999)
Curr. Opin. Struct. Biol
, vol.9
, pp. 530-535
-
-
Kirshenbaum, K.1
Zuckermann, R.N.2
Dill, K.A.3
-
17
-
-
0032705432
-
-
(c) Stigers, K. D.; Soth, M. J.; Nowick, J. S. Curr. Opin. Chem. Biol. 1999, 3, 714-723.
-
(1999)
Curr. Opin. Chem. Biol
, vol.3
, pp. 714-723
-
-
Stigers, K.D.1
Soth, M.J.2
Nowick, J.S.3
-
18
-
-
0035542909
-
-
(d) Hill, D. J.; Mio, M. J.; Prince, R. B.; Hughes, T. S.; Moore, J. S. Chem. Rev. 2001, 101, 3893-4012.
-
(2001)
Chem. Rev
, vol.101
, pp. 3893-4012
-
-
Hill, D.J.1
Mio, M.J.2
Prince, R.B.3
Hughes, T.S.4
Moore, J.S.5
-
30
-
-
33748993139
-
-
Ryu, E.-H.; Yan, J.; Zhong, Z.; Zhao, Y. J. Org. Chem. 2006, 71, 7205-7213.
-
(2006)
J. Org. Chem
, vol.71
, pp. 7205-7213
-
-
Ryu, E.-H.1
Yan, J.2
Zhong, Z.3
Zhao, Y.4
-
31
-
-
4043135772
-
-
For some recent examples of interconvertible unimolecular micelles and reversed micelles, see: a
-
For some recent examples of interconvertible unimolecular micelles and reversed micelles, see: (a) Basu, S.; Vutukuri, D. R.; Shyamroy, S.; Sandanaraj, B. S.; Thayumanavan, S. J. Am. Chem. Soc. 2004, 126, 9890-9891.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 9890-9891
-
-
Basu, S.1
Vutukuri, D.R.2
Shyamroy, S.3
Sandanaraj, B.S.4
Thayumanavan, S.5
-
32
-
-
10044232693
-
-
(b) Vutukuri, D. R.; Basu, S.; Thayumanavan, S. J. Am. Chem. Soc. 2004, 126, 15636-15637.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 15636-15637
-
-
Vutukuri, D.R.1
Basu, S.2
Thayumanavan, S.3
-
34
-
-
0003641908
-
-
Kadish, K. M, Smith, K. M, Guilard, R, Eds, Academic Press: New York
-
(a) The Porphyrin Handbook; Kadish, K. M., Smith, K. M., Guilard, R., Eds.; Academic Press: New York, 2000; Vol. 4.
-
(2000)
The Porphyrin Handbook
, vol.4
-
-
-
35
-
-
1942474160
-
-
(b) Wolf, J. R.; Hamaker, C. G.; Djukic, J.-P.; Kodadek, T.; Woo, L. K. J. Am. Chem. Soc. 1995, 117, 9194-9199.
-
(1995)
J. Am. Chem. Soc
, vol.117
, pp. 9194-9199
-
-
Wolf, J.R.1
Hamaker, C.G.2
Djukic, J.-P.3
Kodadek, T.4
Woo, L.K.5
-
36
-
-
0035956477
-
-
(c) Hamaker, C. G.; Djukic, J.-P.; Daniel, A. S.; Woo, L. K. Organometallics 2001, 20, 5189-5199.
-
(2001)
Organometallics
, vol.20
, pp. 5189-5199
-
-
Hamaker, C.G.1
Djukic, J.-P.2
Daniel, A.S.3
Woo, L.K.4
-
37
-
-
0035956471
-
-
(d) Hamaker, C, G.; Mirafzal, G. A.; Woo, L. K. Organometallics 2001, 20, 5171-5176.
-
(2001)
Organometallics
, vol.20
, pp. 5171-5176
-
-
Hamaker, C.G.1
Mirafzal, G.A.2
Woo, L.K.3
-
38
-
-
0037116501
-
-
(e) Mirafzal, G. A.; Cheng, G.; Woo, L. K. J. Am. Chem. Soc. 2002, 124, 176-177.
-
(2002)
J. Am. Chem. Soc
, vol.124
, pp. 176-177
-
-
Mirafzal, G.A.1
Cheng, G.2
Woo, L.K.3
-
39
-
-
0000052647
-
-
Kadish, K. M, Smith, K. M, Guilard, R, Eds, Academic Press: New York, Chapter 5, pp
-
Jaquinod, L. In The Porphyrin Handbook; Kadish, K. M., Smith, K. M., Guilard, R., Eds.; Academic Press: New York, 2000; Vol. 1, Chapter 5, pp 201-238.
-
(2000)
The Porphyrin Handbook
, vol.1
, pp. 201-238
-
-
Jaquinod, L.1
-
40
-
-
0024559946
-
-
For another steroid-functionalized porphyrin, see
-
For another steroid-functionalized porphyrin, see: Groves, J. T.; Neumann, R. J. Am. Chem. Soc. 1989, 111, 2900-2909.
-
(1989)
J. Am. Chem. Soc
, vol.111
, pp. 2900-2909
-
-
Groves, J.T.1
Neumann, R.2
-
41
-
-
33846641075
-
-
Using local steric and chiral environments to control the selectivity/ activity of metalloporphyrins has been reported; see: (a) Suslick, K. S. In The Porphvrin Handbook; Kadish, K. M, Smith, K. M, Guilard, R, Eds, Academic Press: New York, 2000; 4, Chapter 28, pp 41-63
-
Using local steric and chiral environments to control the selectivity/ activity of metalloporphyrins has been reported; see: (a) Suslick, K. S. In The Porphvrin Handbook; Kadish, K. M., Smith, K. M., Guilard, R., Eds.; Academic Press: New York, 2000; Vol. 4, Chapter 28, pp 41-63.
-
-
-
-
42
-
-
4544250087
-
-
Kadish, K. M, Smith, K. M, Guilard, R, Eds, Academic Press: New York, Chapter 64, pp
-
(b) Marchon, J.-C.; Ramasseul, R. In The Porphyrin Handbook; Kadish, K. M., Smith, K. M., Guilard, R., Eds.; Academic Press: New York, 2000; Vol. 11, Chapter 64, pp 75-132.
-
(2000)
The Porphyrin Handbook
, vol.11
, pp. 75-132
-
-
Marchon, J.-C.1
Ramasseul, R.2
-
43
-
-
0006368032
-
-
For general procedures for acid-catalyzed synthesis of porphyrins, see: a
-
For general procedures for acid-catalyzed synthesis of porphyrins, see: (a) Lindsey, J. S.; Schreiman, C. I.; Hsu, H. C.; Kearney, P. C.; Marguerettaz, A. M. J. Org. Chem. 1987, 52, 827-836.
-
(1987)
J. Org. Chem
, vol.52
, pp. 827-836
-
-
Lindsey, J.S.1
Schreiman, C.I.2
Hsu, H.C.3
Kearney, P.C.4
Marguerettaz, A.M.5
-
46
-
-
33846641074
-
-
Kadish, K. M, Smith, K. M, Guilard, R, Eds, Academic Press: New York, Chapter 15, pp
-
Sanders, J. K. M.; Bampos, N.; Clyde-Watson, Z.; Darling, S. L.; Hawley, J. C.; Kim, H.-J.; Mak, C. C.; Webb, S. M. In The Porphyrin Handbook; Kadish, K. M., Smith, K. M., Guilard, R., Eds.; Academic Press: New York, 2000; Vol. 3, Chapter 15, pp 33.
-
(2000)
The Porphyrin Handbook
, vol.3
, pp. 33
-
-
Sanders, J.K.M.1
Bampos, N.2
Clyde-Watson, Z.3
Darling, S.L.4
Hawley, J.C.5
Kim, H.-J.6
Mak, C.C.7
Webb, S.M.8
-
47
-
-
33846634033
-
-
1H NMR spectroscopy indicated that intermolecular aggregation became significant at higher concentrations (ca. 1 mM), especially in low-polarity mixtures (<20% methanol).
-
1H NMR spectroscopy indicated that intermolecular aggregation became significant at higher concentrations (ca. 1 mM), especially in low-polarity mixtures (<20% methanol).
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-
-
-
49
-
-
33846598290
-
-
It should be mentioned that this inherent preference for larger guests by Zn(CFTPP)-as well as the potential hydrogen bonding interaction discussed previously, is also consistent with 8 being a weaker ligand than 7 in polar solvents
-
It should be mentioned that this inherent preference for larger guests by Zn(CFTPP)-as well as the potential hydrogen bonding interaction discussed previously - is also consistent with 8 being a weaker ligand than 7 in polar solvents.
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50
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33846618108
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The yields given are the averages from three separate experiments. The errors are the standard deviations. See Table 2S in the Supporting Information for the actual yields.
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The yields given are the averages from three separate experiments. The errors are the standard deviations. See Table 2S in the Supporting Information for the actual yields.
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-
-
-
51
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33846561913
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1H NMR spectroscopy. It should be mentioned that any potential intermolecular aggregation of Fe(CFTPP)Cl in low polarity solvents would only reduce the contribution of the reversed micelle-like conformer and decrease the substrate selectivity. Therefore, the observed preference for polar substrates should represent the lower limit achievable by the reversed micelle-like conformer.
-
1H NMR spectroscopy. It should be mentioned that any potential intermolecular aggregation of Fe(CFTPP)Cl in low polarity solvents would only reduce the contribution of the reversed micelle-like conformer and decrease the substrate selectivity. Therefore, the observed preference for polar substrates should represent the lower limit achievable by the reversed micelle-like conformer.
-
-
-
-
52
-
-
0020581268
-
-
Bellini, A. M.; Quaglio, M. P.; Guarneri, M.; Cavazzini, G. Eur. J. Med. Chem. 1983, 18, 185-190.
-
(1983)
Eur. J. Med. Chem
, vol.18
, pp. 185-190
-
-
Bellini, A.M.1
Quaglio, M.P.2
Guarneri, M.3
Cavazzini, G.4
-
53
-
-
0002036846
-
-
Small discrepancies in the m/z obtained by MALDI-TOFMS were sometimes observed in compounds containing multiple cholates. Similar behavior was reported in the literature; see: Zuluaga, F.; Valderruten, N. E.; Wagener K, B. Polym. Bull. 1999, 42, 41-46.
-
Small discrepancies in the m/z obtained by MALDI-TOFMS were sometimes observed in compounds containing multiple cholates. Similar behavior was reported in the literature; see: Zuluaga, F.; Valderruten, N. E.; Wagener K, B. Polym. Bull. 1999, 42, 41-46.
-
-
-
-
54
-
-
0036741318
-
-
Van Manen, H-J.; Fokkens, R. H.; Van Veggel, F. C. J. M.; Reinhoudt, D. N. Eur. J. Org. Chem. 2002, 18, 3189-3197.
-
(2002)
Eur. J. Org. Chem
, vol.18
, pp. 3189-3197
-
-
Van Manen, H.-J.1
Fokkens, R.H.2
Van Veggel, F.C.J.M.3
Reinhoudt, D.N.4
-
55
-
-
0016856701
-
-
(a) Collman, J. P.; Gagne, R. R.; Reed, C. A.; Halbert, T. R.; Lang, G.; Robinson, W. T. J. Am. Chem. Soc. 1975, 97, 1427-1439.
-
(1975)
J. Am. Chem. Soc
, vol.97
, pp. 1427-1439
-
-
Collman, J.P.1
Gagne, R.R.2
Reed, C.A.3
Halbert, T.R.4
Lang, G.5
Robinson, W.T.6
-
56
-
-
0000660410
-
-
(b) Kobayashi, H.; Higuchi, T.; Kaizu, Y.; Osada, H.; Aoki, M. Bull. Chem. Soc. Jpn. 1975, 48(11), 3137.
-
(1975)
Bull. Chem. Soc. Jpn
, vol.48
, Issue.11
, pp. 3137
-
-
Kobayashi, H.1
Higuchi, T.2
Kaizu, Y.3
Osada, H.4
Aoki, M.5
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