-
1
-
-
76549252207
-
-
a) L. Pauling, R. B. Corey, H. R. Branson, Proc. Natl. Acad. Sci USA 1951, 37, 205;
-
(1951)
Proc. Natl. Acad. Sci USA
, vol.37
, pp. 205
-
-
Pauling, L.1
Corey, R.B.2
Branson, H.R.3
-
2
-
-
52149116532
-
-
b) S. Aravinda, N. Shamala, P. Balaram, Chem. Biodiversity 2008, 5, 1238.
-
(2008)
Chem. Biodiversity
, vol.5
, pp. 1238
-
-
Aravinda, S.1
Shamala, N.2
Balaram, P.3
-
3
-
-
0024700331
-
-
a) V. Moretto, M. Crisma, G. M. Bonora, C. Toniolo, H. Balaram, P. Balaram, Macromolecules 1989, 22, 2939;
-
(1989)
Macromolecules
, vol.22
, pp. 2939
-
-
Moretto, V.1
Crisma, M.2
Bonora, G.M.3
Toniolo, C.4
Balaram, H.5
Balaram, P.6
-
5
-
-
0028908985
-
-
c) J. D. Aug-spurger, V. A. Bindra, H. A. Scheraga, A. Kuki, Biochemistry 1995, 34, 2566;
-
(1995)
Biochemistry
, vol.34
, pp. 2566
-
-
Aug-spurger, J.D.1
Bindra, V.A.2
Scheraga, H.A.3
Kuki, A.4
-
6
-
-
0345352748
-
-
d) J. R. Kumita, C. J. Weston, L.-P. Choo-Smith, G. A. Woolley, O. S. Smart, Biochemistry 2003, 42, 4492;
-
(2003)
Biochemistry
, vol.42
, pp. 4492
-
-
Kumita, J.R.1
Weston, C.J.2
Choo-Smith, L.-P.3
Woolley, G.A.4
Smart, O.S.5
-
7
-
-
0035471131
-
-
e) J. Venkatraman, S. C. Shankaramma, P. Balaram, Chem. Rev. 2001, 101, 3131.
-
(2001)
Chem. Rev
, vol.101
, pp. 3131
-
-
Venkatraman, J.1
Shankaramma, S.C.2
Balaram, P.3
-
8
-
-
0035552035
-
-
a) C. Toniolo, M. Crisma, F. Formaggio, C. Peggion, Biopolymers 2001, 60, 396;
-
(2001)
Biopolymers
, vol.60
, pp. 396
-
-
Toniolo, C.1
Crisma, M.2
Formaggio, F.3
Peggion, C.4
-
9
-
-
0026035625
-
-
b) C. Toniolo, M. Crisma, G. M. Bonora, E. Benedetti, B. di Blasio, V. Pavone, C. Pedone, A. Santini, Biopolymers 1991, 31, 129.
-
(1991)
Biopolymers
, vol.31
, pp. 129
-
-
Toniolo, C.1
Crisma, M.2
Bonora, G.M.3
Benedetti, E.4
di Blasio, B.5
Pavone, V.6
Pedone, C.7
Santini, A.8
-
10
-
-
0242660256
-
-
a) R.-P. Hummel, C. Toniolo, G. Jung, Angew. Chem. 1987, 99, 1180;
-
(1987)
Angew. Chem
, vol.99
, pp. 1180
-
-
Hummel, R.-P.1
Toniolo, C.2
Jung, G.3
-
14
-
-
6744266061
-
-
b) M. M. Green, N. C. Peterson, T. Sato, A. Teramoto, R. Cook, S. Lifson, Science 1995, 268, 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
-
15
-
-
0003080761
-
-
B. Pengo, F. Formaggio, M. Crisma, C. Toniolo, G. M. Bonora, Q. B. Broxterman, J. Kamphuis, M. Savino, R. Iacovino, F. Rossi, E. Benedetti, J. Chem. Soc. Perkin Trans. 2 1998, 1651.
-
(1998)
J. Chem. Soc. Perkin Trans. 2
, pp. 1651
-
-
Pengo, B.1
Formaggio, F.2
Crisma, M.3
Toniolo, C.4
Bonora, G.M.5
Broxterman, Q.B.6
Kamphuis, J.7
Savino, M.8
Iacovino, R.9
Rossi, F.10
Benedetti, E.11
-
16
-
-
0032920764
-
-
a) Y. Inai, Y. Kurokawa, T. Hirabashi, Biopolymers 1999, 49, 551;
-
(1999)
Biopolymers
, vol.49
, pp. 551
-
-
Inai, Y.1
Kurokawa, Y.2
Hirabashi, T.3
-
17
-
-
0032890855
-
-
b) Y Inai, Y. Kurokawa, A. Ida, T. Hirabashi, Bull. Chem. Soc. Jpn. 1999, 72, 55.
-
(1999)
Bull. Chem. Soc. Jpn
, vol.72
, pp. 55
-
-
Inai, Y.1
Kurokawa, Y.2
Ida, A.3
Hirabashi, T.4
-
18
-
-
0034731013
-
-
a) Y. Inai, K. Tagawa, A. Takasu, T. Hirabayashi, T. Oshikawa, M. Yanashita, J. Am. Chem. Soc. 2000, 122, 11731;
-
(2000)
J. Am. Chem. Soc
, vol.122
, pp. 11731
-
-
Inai, Y.1
Tagawa, K.2
Takasu, A.3
Hirabayashi, T.4
Oshikawa, T.5
Yanashita, M.6
-
19
-
-
0038006011
-
-
b) Y. Inai, N. Ousaka, T. Okabe, J. Am. Chem. Soc. 2003, 125, 8151;
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 8151
-
-
Inai, Y.1
Ousaka, N.2
Okabe, T.3
-
21
-
-
0035781183
-
-
For examples of helicity controlled from one terminus of nonpeptide structures, see; a T. Nakano, Y. Okamoto, Chem. Rev. 2001, 101, 4013;
-
For examples of helicity controlled from one terminus of nonpeptide structures, see; a) T. Nakano, Y. Okamoto, Chem. Rev. 2001, 101, 4013;
-
-
-
-
22
-
-
70349895195
-
-
b) D. J. Hill, M. J. Mio, R. B. Prince, T. S. Hughes, J. S. Moore, Chem. Rev. 2001, 101, 3993;
-
(2001)
Chem. Rev
, vol.101
, pp. 3993
-
-
Hill, D.J.1
Mio, M.J.2
Prince, R.B.3
Hughes, T.S.4
Moore, J.S.5
-
23
-
-
0942298051
-
-
c) H. Jiang, C. Dolain, J.-M. Leger, H. Gornitzka, I. Huc, J. Am. Chem. Soc. 2004, 126. 1034;
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 1034
-
-
Jiang, H.1
Dolain, C.2
Leger, J.-M.3
Gornitzka, H.4
Huc, I.5
-
24
-
-
57349142448
-
-
d) I Clayden, L. Lemiegre, G. A. Morris, M. Pickworth, T. J. Snape, L. H. Jones, J. Am. Chem. Soc. 2008, 130, 15193.
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 15193
-
-
Clayden, I.1
Lemiegre, L.2
Morris, G.A.3
Pickworth, M.4
Snape, T.J.5
Jones, L.H.6
-
25
-
-
33748775187
-
-
Contrasting chromophores have been used to quantify helicity in different segments of a helical oligomer Ref, 8c, and the chain-length dependence of a CD signal has been used to estimate the degree of order in a polyisocyanate carrying a chiral terminator: G. Y. Nath, S. Samal, S.-Y. Park, C. N. Murthy, J.-S. Lee, Macromolecules 2006, 39, 5965
-
Contrasting chromophores have been used to quantify helicity in different segments of a helical oligomer (Ref. [8c]) and the chain-length dependence of a CD signal has been used to estimate the degree of order in a polyisocyanate carrying a chiral terminator: G. Y. Nath, S. Samal, S.-Y. Park, C. N. Murthy, J.-S. Lee, Macromolecules 2006, 39, 5965.
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-
-
-
26
-
-
40149092410
-
-
Helices containing only achiral amino acids but which invert slowly on the NMR timescale would of course exhibit anisochronous signals, see; a N. Ousaka, T. Sato, R. Kuroda, J. Am. Chem. Soc. 2008, 130, 463;
-
Helices containing only achiral amino acids but which invert slowly on the NMR timescale would of course exhibit anisochronous signals, see; a) N. Ousaka, T. Sato, R. Kuroda, J. Am. Chem. Soc. 2008, 130, 463;
-
-
-
-
27
-
-
4043138620
-
-
b) V. Maurizot, C. Dolain, Y. Leydet, J.-M. Léger, P. Guionneau, I. Huc, J. Am. Chem. Soc. 2004, 126, 10049;
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 10049
-
-
Maurizot, V.1
Dolain, C.2
Leydet, Y.3
Léger, J.-M.4
Guionneau, P.5
Huc, I.6
-
28
-
-
25144474487
-
-
Helix preference in structures of this type has been controlled by a single terminal residue, see; c
-
Helix preference in structures of this type has been controlled by a single terminal residue, see; c) J.-M. Léger, P. Guionneau, I. Huc, J. Am. Chem. Soc. 2005, 127, 12943.
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 12943
-
-
Léger, J.-M.1
Guionneau, P.2
Huc, I.3
-
29
-
-
70349895191
-
-
The choice of Cbz-L-Phe as the helix controller was made after a brief survey of amino acids, in which this terminator performed exceptionally well, presumably because it maximizes the difference in stability between the two diastereomeric helices, and consequently the chemical-shift difference observed in the reporter
-
The choice of Cbz-L-Phe as the helix controller was made after a brief survey of amino acids, in which this terminator performed exceptionally well, presumably because it maximizes the difference in stability between the two diastereomeric helices, and consequently the chemical-shift difference observed in the reporter.
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-
-
30
-
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70349897315
-
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2OR analogues showed poor anisochronicity, perhaps due to freer bond rotation in the absence of a C-terminal hydrogen bond.
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2OR analogues showed poor anisochronicity, perhaps due to freer bond rotation in the absence of a C-terminal hydrogen bond.
-
-
-
-
31
-
-
0001947018
-
-
M. T. Leplawy, D. S. Jones, G. W. Kenner, R. C. Sheppard, Tetrahedron 1960, 11, 39;
-
(1960)
Tetrahedron
, vol.11
, pp. 39
-
-
Leplawy, M.T.1
Jones, D.S.2
Kenner, G.W.3
Sheppard, R.C.4
-
32
-
-
37049062259
-
-
D. S. Jones, G. W. Kenner, J. Preston, R. C. Sheppard, J. Chem. Soc. 1965, 6227;
-
(1965)
J. Chem. Soc
, pp. 6227
-
-
Jones, D.S.1
Kenner, G.W.2
Preston, J.3
Sheppard, R.C.4
-
33
-
-
0026010908
-
-
E. Frérot, J. Coste, A. Pantaloni, M.-N. Dufour, P. Jouin, Tetrahedron 1991, 47, 259;
-
(1991)
Tetrahedron
, vol.47
, pp. 259
-
-
Frérot, E.1
Coste, J.2
Pantaloni, A.3
Dufour, M.-N.4
Jouin, P.5
-
34
-
-
0030903994
-
-
M. Meldal, M. A. Juliano, A. N. Jansson, Tetrahedron Lett. 1997, 38, 2531;
-
(1997)
Tetrahedron Lett
, vol.38
, pp. 2531
-
-
Meldal, M.1
Juliano, M.A.2
Jansson, A.N.3
-
35
-
-
0346423686
-
-
M. Jost, J.-G Greie, N. Stemmer, S. D. Wilking, K. Altendorf, N. Sewald, Angew. Chem. 2002, 114, 4438;
-
(2002)
Angew. Chem
, vol.114
, pp. 4438
-
-
Jost, M.1
Greie, J.-G.2
Stemmer, N.3
Wilking, S.D.4
Altendorf, K.5
Sewald, N.6
-
37
-
-
70349897318
-
-
3 were broad and concentration-dependent, suggesting aggregation in this solvent.
-
3 were broad and concentration-dependent, suggesting aggregation in this solvent.
-
-
-
-
38
-
-
70349934385
-
-
Between -20 and - 50 °C, increased broadening of these singlets suggests that the rate of helix inversion approaches the slow-exchange regime only below -50°C; see ref. [4].
-
Between -20 and - 50 °C, increased broadening of these singlets suggests that the rate of helix inversion approaches the slow-exchange regime only below -50°C; see ref. [4].
-
-
-
-
39
-
-
28044445674
-
-
For a related idea, see
-
For a related idea, see: C. Dolain, J.-M. Léger, N. Delsuc, H. Gornitzka, I. Huc, Proc. Natl. Acad. Sci. USA 2005, 102, 16146.
-
(2005)
Proc. Natl. Acad. Sci. USA
, vol.102
, pp. 16146
-
-
Dolain, C.1
Léger, J.-M.2
Delsuc, N.3
Gornitzka, H.4
Huc, I.5
-
40
-
-
0028262457
-
-
C. Toniolo, F. Formaggio, M. Crisma, H. E. Schoemaker, J. Kamphuis, Tetrahedron: Asymmetry 1994, 5, 507.
-
(1994)
Tetrahedron: Asymmetry
, vol.5
, pp. 507
-
-
Toniolo, C.1
Formaggio, F.2
Crisma, M.3
Schoemaker, H.E.4
Kamphuis, J.5
-
42
-
-
0242343206
-
-
b) R. Gessmann, H. Bruckner, K. Petratos, J. Peptide Sci. 2003, 9, 753.
-
(2003)
J. Peptide Sci
, vol.9
, pp. 753
-
-
Gessmann, R.1
Bruckner, H.2
Petratos, K.3
-
44
-
-
7244228083
-
-
b) J. Clayden, A. Lund, L. Vallverdú, M. Helliwell, Nature 2004, 431, 966;
-
(2004)
Nature
, vol.431
, pp. 966
-
-
Clayden, J.1
Lund, A.2
Vallverdú, L.3
Helliwell, M.4
-
45
-
-
61349093028
-
-
4Gly is identical with that of 11-14; see Ref. [1b].
-
4Gly is identical with that of 11-14; see Ref. [1b].
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