-
2
-
-
0004139082
-
-
in, Krieger Publishing Company, Malabar, FL
-
J. Jacquws, A. Collet and S. H. Wilen, in Enantiomers, Racemates, and Resolutions, Krieger Publishing Company, Malabar, FL, 1994
-
(1994)
Enantiomers, Racemates, and Resolutions
-
-
Jacquws, J.1
Collet, A.2
Wilen, S.H.3
-
3
-
-
0003461218
-
-
in, ed. D. N. Reinhoudt, Pergamon, Oxford, 113-149
-
A. Collet, in Comprehensive Supramolecular Chemistry, ed., D. N. Reinhoudt, Pergamon, Oxford, 1996, vol. 10, pp. 113-149
-
(1996)
Comprehensive Supramolecular Chemistry
, vol.10
-
-
Collet, A.1
-
9
-
-
79959189562
-
-
M. M. S-Sempere P. Osswald M. Stolte M. Grüne M. Renz M. Kaupp K. Radacki H. Braunschweig F. Würthner J. Am. Chem. Soc. 2011 133 9580 9591
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 9580-9591
-
-
S-Sempere, M.M.1
Osswald, P.2
Stolte, M.3
Grüne, M.4
Renz, M.5
Kaupp, M.6
Radacki, K.7
Braunschweig, H.8
Würthner, F.9
-
16
-
-
4043072677
-
-
V. Percec A. E. Dulcey V. S. K. Balagurusamy Y. Miura J. Smidrkal M. Peterca S. Nummelin U. Edlund S. D. Hudson P. A. Heiney H. Duan S. N. Magonov S. A. Vinogradov Nature 2004 430 764 768
-
(2004)
Nature
, vol.430
, pp. 764-768
-
-
Percec, V.1
Dulcey, A.E.2
Balagurusamy, V.S.K.3
Miura, Y.4
Smidrkal, J.5
Peterca, M.6
Nummelin, S.7
Edlund, U.8
Hudson, S.D.9
Heiney, P.A.10
Duan, H.11
Magonov, S.N.12
Vinogradov, S.A.13
-
17
-
-
2642574190
-
-
J. P. Hill W. Jin A. Kosaka T. Fukushima H. Ichihara T. Shimomura K. Itoh T. Hashizume N. Ishii T. Aida Science 2004 304 1481 1483
-
(2004)
Science
, vol.304
, pp. 1481-1483
-
-
Hill, J.P.1
Jin, W.2
Kosaka, A.3
Fukushima, T.4
Ichihara, H.5
Shimomura, T.6
Itoh, K.7
Hashizume, T.8
Ishii, N.9
Aida, T.10
-
20
-
-
84866438615
-
-
Z. Huang S.-K. Kang M. Banno T. Yamaguchi D. Lee C. Seok E. Yashima M. Lee Science 2012 337 1521 1526
-
(2012)
Science
, vol.337
, pp. 1521-1526
-
-
Huang, Z.1
Kang, S.-K.2
Banno, M.3
Yamaguchi, T.4
Lee, D.5
Seok, C.6
Yashima, E.7
Lee, M.8
-
23
-
-
83055179339
-
-
Y. Yang W. Feng J. Hu S. Zou R. Gao K. Yamato M. Kline Z. Cai Y. Gao Y. Wang Y. Li Y. Yang L. Yuan X. C. Zeng B. Gong J. Am. Chem. Soc. 2011 133 18590 18593
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 18590-18593
-
-
Yang, Y.1
Feng, W.2
Hu, J.3
Zou, S.4
Gao, R.5
Yamato, K.6
Kline, M.7
Cai, Z.8
Gao, Y.9
Wang, Y.10
Li, Y.11
Yang, Y.12
Yuan, L.13
Zeng, X.C.14
Gong, B.15
-
24
-
-
79952674661
-
-
M. Fritzsche A. Bohle D. Dudenko U. Baumeister D. Sebastiani G. Richardt H. W. Spiess M. R. Hansen S. Höger Angew. Chem., Int. Ed. 2011 50 3030 3033
-
(2011)
Angew. Chem., Int. Ed.
, vol.50
, pp. 3030-3033
-
-
Fritzsche, M.1
Bohle, A.2
Dudenko, D.3
Baumeister, U.4
Sebastiani, D.5
Richardt, G.6
Spiess, H.W.7
Hansen, M.R.8
Höger, S.9
-
25
-
-
0000314051
-
-
P. Wipf Chem. Rev. 1995 95 2115 2134
-
(1995)
Chem. Rev.
, vol.95
, pp. 2115-2134
-
-
Wipf, P.1
-
32
-
-
84857319239
-
-
Fig. 3c shows that the elution volume of a homochiral polymer formed with (R)- 1 at [(R)- 1] = 0.50 mM is 17.7 mL. If chiral self-sorting indeed occurs ideally, the elution volume should remain unchanged even when the same amount of its enantiomer ([(S)- 1] = 0.50 mM) is added. However, the observed value (16.4 mL), read out from Fig. 6c at [(S)- 1] = [(R)- 1] = 0.50 mM for the stereochemical copolymerization, is 1.3 mL smaller than 17.7 mL
-
T. Aida E. W. Meijer S. I. Stupp Science 2012 335 813 817
-
(2012)
Science
, vol.335
, pp. 813-817
-
-
Aida, T.1
Meijer, E.W.2
Stupp, S.I.3
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