-
2
-
-
0032476790
-
-
E. Uhlmann, A. Peyman, G. Breipohl, and D.W. Will Angew. Chem., Int. Ed. 37 1998 2797 2823
-
(1998)
Angew. Chem., Int. Ed.
, vol.37
, pp. 2797-2823
-
-
Uhlmann, E.1
Peyman, A.2
Breipohl, G.3
Will, D.W.4
-
12
-
-
33746904737
-
-
A. Dragulescu-Andrasi, S. Rapireddy, B.M. Frezza, C. Gayathri, R.R. Gil, and D.H. Ly J. Am. Chem. Soc. 128 2006 10258 10267
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 10258-10267
-
-
Dragulescu-Andrasi, A.1
Rapireddy, S.2
Frezza, B.M.3
Gayathri, C.4
Gil, R.R.5
Ly, D.H.6
-
20
-
-
0037450406
-
-
T. Vilaivan, C. Suparpprom, P. Duanglaor, P. Harnyuttanakorn, and G. Lowe Tetrahedron Lett. 44 2003 1663 1666
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 1663-1666
-
-
Vilaivan, T.1
Suparpprom, C.2
Duanglaor, P.3
Harnyuttanakorn, P.4
Lowe, G.5
-
22
-
-
0023651248
-
-
F. Morvan, B. Rayner, J.L. Imbach, M. Lee, J.A. Hartley, D.K. Chang, and J.W. Lown Nucleic Acids Res. 15 1987 7027 7044
-
(1987)
Nucleic Acids Res.
, vol.15
, pp. 7027-7044
-
-
Morvan, F.1
Rayner, B.2
Imbach, J.L.3
Lee, M.4
Hartley, J.A.5
Chang, D.K.6
Lown, J.W.7
-
24
-
-
0033230088
-
-
A. Laurent, M. Naval, F. Debart, J.-J. Vasseur, and B. Rayner Nucleic Acids Res. 27 1999 4151 4159
-
(1999)
Nucleic Acids Res.
, vol.27
, pp. 4151-4159
-
-
Laurent, A.1
Naval, M.2
Debart, F.3
Vasseur, J.-J.4
Rayner, B.5
-
25
-
-
0023392854
-
-
N.T. Thuong, U. Asseline, V. Roig, M. Takasugi, and C. Hélne Proc. Natl. Acad. Sci. U.S.A. 84 1987 5129 5133
-
(1987)
Proc. Natl. Acad. Sci. U.S.A.
, vol.84
, pp. 5129-5133
-
-
Thuong, N.T.1
Asseline, U.2
Roig, V.3
Takasugi, M.4
Hélne, C.5
-
27
-
-
77957660737
-
-
note
-
2(3′) rotamers], 3.44-3.49 and 3.73-3.82
-
-
-
-
29
-
-
77957658556
-
-
The pentafluorophenyl esters were generated from the corresponding Fmoc free acids by treatment with pentafluorophenyl trifluoroacetate/DIEA. The unstable active esters were used following an acid-base extraction to remove DIEA salts without further purification.
-
The pentafluorophenyl esters were generated from the corresponding Fmoc free acids by treatment with pentafluorophenyl trifluoroacetate/DIEA. The unstable active esters were used following an acid-base extraction to remove DIEA salts without further purification.
-
-
-
-
31
-
-
77957678160
-
-
2·DNA hybrids, it was established from our previous titration experiments (Refs. 7a-d) that homothymine pyrrolidinyl PNA forms only 1:1 hybrids with DNA.
-
2·DNA hybrids, it was established from our previous titration experiments (Refs. 7a-d ) that homothymine pyrrolidinyl PNA forms only 1:1 hybrids with DNA.
-
-
-
-
32
-
-
77957665838
-
-
Heating of single-stranded (2′R,4′S)-acpcPNA with a non-self-complementary sequence such as P1 resulted in no melting curve. This rules out the possibilities of intramolecular folding or non-specific aggregate formation such as those observed in aegPNA.
-
Heating of single-stranded (2′R,4′S)-acpcPNA with a non-self-complementary sequence such as P1 resulted in no melting curve. This rules out the possibilities of intramolecular folding or non-specific aggregate formation such as those observed in aegPNA.
-
-
-
-
36
-
-
55549100250
-
-
B. Boontha, J. Nakkuntod, N. Hirankarn, P. Chaumpluk, and T. Vilaivan Anal. Chem. 80 2008 8178 8186
-
(2008)
Anal. Chem.
, vol.80
, pp. 8178-8186
-
-
Boontha, B.1
Nakkuntod, J.2
Hirankarn, N.3
Chaumpluk, P.4
Vilaivan, T.5
-
39
-
-
41149158074
-
-
T. Ishizuka, J. Yoshida, Y. Yamamoto, J. Sumaoka, T. Tedeschi, R. Corradini, S. Sforza, and M. Komiyama Nucleic Acids Res. 36 2008 1464 1471
-
(2008)
Nucleic Acids Res.
, vol.36
, pp. 1464-1471
-
-
Ishizuka, T.1
Yoshida, J.2
Yamamoto, Y.3
Sumaoka, J.4
Tedeschi, T.5
Corradini, R.6
Sforza, S.7
Komiyama, M.8
|