-
3
-
-
0041365966
-
-
L.E. Ernest H.W. Samuel John Wiley and Sons New York
-
For recent reviews, see: M. Farina L.E. Ernest H.W. Samuel Topics in Stereochemistry Vol. 17 1987 John Wiley and Sons New York
-
(1987)
Topics in Stereochemistry
, vol.17
-
-
Farina, M.1
-
6
-
-
6744266061
-
-
M.M. Green, N.C. Peterson, T. Sato, A. Teramoto, R. Cook, and S. Lifson Science 268 1995 1860
-
(1995)
Science
, vol.268
, pp. 1860
-
-
Green, M.M.1
Peterson, N.C.2
Sato, T.3
Teramoto, A.4
Cook, R.5
Lifson, S.6
-
9
-
-
0000718373
-
-
L. Pu Chem. Rev. 98 1998 2405
-
(1998)
Chem. Rev.
, vol.98
, pp. 2405
-
-
Pu, L.1
-
10
-
-
0033517692
-
-
M.M. Green, J.-W. Park, T. Sato, A. Teramoto, S. Lifson, R.L.B. Selinger, and J.V. Selinger Angew. Chem., Int. Ed. 38 1999 3138
-
(1999)
Angew. Chem., Int. Ed.
, vol.38
, pp. 3138
-
-
Green, M.M.1
Park, J.-W.2
Sato, T.3
Teramoto, A.4
Lifson, S.5
Selinger, R.L.B.6
Selinger, J.V.7
-
17
-
-
0035542909
-
-
D.J. Hill, M.J. Mio, R.B. Prince, T.S. Hughes, and J.S. Moore Chem. Rev. 101 2001 3893
-
(2001)
Chem. Rev.
, vol.101
, pp. 3893
-
-
Hill, D.J.1
Mio, M.J.2
Prince, R.B.3
Hughes, T.S.4
Moore, J.S.5
-
22
-
-
14844320755
-
-
H. Onouchi, T. Miyagawa, A. Furuko, K. Maeda, and E. Yashima J. Am. Chem. Soc. 127 2005 2960
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 2960
-
-
Onouchi, H.1
Miyagawa, T.2
Furuko, A.3
Maeda, K.4
Yashima, E.5
-
23
-
-
22744445542
-
-
K. Nagai, K. Maeda, Y. Takeyama, K. Sakajiri, and E. Yashima Macromolecules 38 2005 5444
-
(2005)
Macromolecules
, vol.38
, pp. 5444
-
-
Nagai, K.1
Maeda, K.2
Takeyama, Y.3
Sakajiri, K.4
Yashima, E.5
-
29
-
-
0342763378
-
-
A. Angeloni, M. Laus, D. Caretti, E. Chiellini, and G. Galli Makromol. Chem. 191 1990 2787
-
(1990)
Makromol. Chem.
, vol.191
, pp. 2787
-
-
Angeloni, A.1
Laus, M.2
Caretti, D.3
Chiellini, E.4
Galli, G.5
-
30
-
-
0037117635
-
-
P.K. Bowyer, C.C. Vernon, G.-N. Nahid, P.A. Gugger, A.D. Rae, G.F. Swiegers, A.C. Willis, J. Zank, and S.B. Wild Proc. Natl. Acad. Sci. U.S.A. 99 2002 4877
-
(2002)
Proc. Natl. Acad. Sci. U.S.A.
, vol.99
, pp. 4877
-
-
Bowyer, P.K.1
Vernon, C.C.2
Nahid, G.-N.3
Gugger, P.A.4
Rae, A.D.5
Swiegers, G.F.6
Willis, A.C.7
Zank, J.8
Wild, S.B.9
-
31
-
-
0032564850
-
-
T. Imamoto, J. Watanabe, Y. Wada, H. Masuda, H. Yamada, H. Tsuruta, S. Matsukawa, and K. Yamaguchi J. Am. Chem. Soc. 120 1998 1635
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 1635
-
-
Imamoto, T.1
Watanabe, J.2
Wada, Y.3
Masuda, H.4
Yamada, H.5
Tsuruta, H.6
Matsukawa, S.7
Yamaguchi, K.8
-
32
-
-
24344478989
-
-
note
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+].
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-
-
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33
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24344434349
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note
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The removal of borane from these stable compounds was not carried out, since the primary purpose of this study was to evaluate the conformational behaviors of the optically active oligomer.
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34
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24344489219
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note
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w = 0.114. CCDC-256581 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge via www.ccdc.cam.ac.uk/conts/retrieving.html (or from the Cambridge Crystallographic Data Centre, 12, Union Road Cambridge CB21EZ, UK; fax: (+44) 1223 336 033; or deposit@ccdc.cam.ac.uk ).
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-
-
-
35
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-
0034683049
-
-
Successful synthesis of the first 1,4,7-triphosphacyclononane derivatives, 9-phosphacrown-3 skeleton, was reported, see: P.G. Edwards, P.D. Newman, and K.M. Abdul Malik Angew. Chem., Int. Ed. 39 2000 2922
-
(2000)
Angew. Chem., Int. Ed.
, vol.39
, pp. 2922
-
-
Edwards, P.G.1
Newman, P.D.2
Abdul Malik, K.M.3
-
36
-
-
0034616746
-
-
And several polyphosphamacrocycles have been synthesized using the appropriate templates, for example, see: A.J. Price, and P.G. Edwards Chem. Commun. 2000 899
-
(2000)
Chem. Commun.
, pp. 899
-
-
Price, A.J.1
Edwards, P.G.2
-
38
-
-
0038019502
-
-
N. Avarvari, N. Mézailles, L. Ricard, P.L. Floch, and F. Mathey Science 280 1998 1587
-
(1998)
Science
, vol.280
, pp. 1587
-
-
Avarvari, N.1
Mézailles, N.2
Ricard, L.3
Floch, P.L.4
Mathey, F.5
-
39
-
-
0001592097
-
-
T. Mizuta, A. Okano, T. Sasaki, H. Nakazawa, and K. Miyoshi Inorg. Chem. 36 1997 200
-
(1997)
Inorg. Chem.
, vol.36
, pp. 200
-
-
Mizuta, T.1
Okano, A.2
Sasaki, T.3
Nakazawa, H.4
Miyoshi, K.5
-
40
-
-
0036291388
-
-
von G. Märkl, J. Reisinger, P. Kreitmeier, J. Langer, and H. Nöth Helv. Chim. Acta 85 2002 1714
-
(2002)
Helv. Chim. Acta
, vol.85
, pp. 1714
-
-
Von, M.G.1
Reisinger, J.2
Kreitmeier, P.3
Langer, J.4
Nöth, H.5
-
41
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24344459267
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note
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g as the second cycle.
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42
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24344452739
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note
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The octamer (S,R,S,R,R,S,R,S)-3 exhibited decomposition at around 220°C according to the thermogravimetric analysis (TGA).
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43
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24344458729
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note
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Although a circular dichromism (CD) spectrometer is a powerful tool for the studies on the dynamics of a chiral compound in solution, compounds 1-3 do not absorb light in the appropriate UV range.
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44
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24344448847
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note
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3): see Ref. 8. This information speculates that chiral phosphorus atoms rotate the plane of polarized light counterclockwise, and higher-order structure in the present system rotates it clockwise.
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