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6
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0032473890
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Koshkin A.A., Singh S.K., Nielsen P., Rajwanshi V.K., Kumar R., Meldgaard M., Olsen C.E., Wengel J. Tetrahedron. 54:1998;3607.
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Tetrahedron
, vol.54
, pp. 3607
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-
Koshkin, A.A.1
Singh, S.K.2
Nielsen, P.3
Rajwanshi, V.K.4
Kumar, R.5
Meldgaard, M.6
Olsen, C.E.7
Wengel, J.8
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7
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0032560835
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Obika S., Nanbu D., Hari Y., Andoh J., Morio K., Doi T., Imanishi T. Tetrahedron Lett. 39:1998;5401.
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, pp. 5401
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-
Obika, S.1
Nanbu, D.2
Hari, Y.3
Andoh, J.4
Morio, K.5
Doi, T.6
Imanishi, T.7
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11
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0027479864
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Kawasaki A.M., Casper M.D., Freier S.M., Lesnik E.A., Zounes M.C., Cummins L.L., Gonzales C., Cook P.D. J. Med. Chem. 36:1993;831.
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Kawasaki, A.M.1
Casper, M.D.2
Freier, S.M.3
Lesnik, E.A.4
Zounes, M.C.5
Cummins, L.L.6
Gonzales, C.7
Cook, P.D.8
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18
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85031147028
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note
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m values) are discussed relative to the corresponding reference duplex formed by hybridization between two unmodified (DNA or RNA) complementary strands.
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-
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19
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0027369575
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Svendsen M.L., Wengel J., Dahl O., Kirpekar F., Roepstorff P. Tetrahedron. 49:1993;11341.
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(1993)
Tetrahedron
, vol.49
, pp. 11341
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-
Svendsen, M.L.1
Wengel, J.2
Dahl, O.3
Kirpekar, F.4
Roepstorff, P.5
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20
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33746390946
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Rajwanshi V.K., Kumar R., Kofod-Hansen M., Wengel J. J. Chem. Soc., Perkin Trans. 1. 1999;1407.
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(1999)
J. Chem. Soc., Perkin Trans. 1
, pp. 1407
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Rajwanshi, V.K.1
Kumar, R.2
Kofod-Hansen, M.3
Wengel, J.4
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23
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85031154743
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note
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The term 'XNA' is defined herein as an oligonucleotide containing one or more xylo-configured nucleotide monomers ('XNA-monomer(s)').
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-
-
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24
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0034755868
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We used sodium hydroxide instead of lithium hydroxide during reaction on the 3′-O-mesylated intermediate
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Kong J.P., Kim S.K., Moon B.J., Kim S.J., Kim H.B. Nucleosides Nucleotides. 20:2001;1751. We used sodium hydroxide instead of lithium hydroxide during reaction on the 3′-O-mesylated intermediate.
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(2001)
Nucleosides Nucleotides
, vol.20
, pp. 1751
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Kong, J.P.1
Kim, S.K.2
Moon, B.J.3
Kim, S.J.4
Kim, H.B.5
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26
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85031151766
-
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note
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3OD; selected signals) δ 138.5, 111.0, 100.7 (J=184.9), 90.4 (J=38.4), 85.0, 73.8 (J=25.8), 60.7, 12.6.
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-
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30
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0025879048
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and references cited therein
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Mikhailopulo I.A., Poopeiko N.E., Pricota T.I., Sivets G.G., Kvasyuk E.I., Balzarini J., De Clercq E. J. Med. Chem. 34:1991;2195. and references cited therein.
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(1991)
J. Med. Chem.
, vol.34
, pp. 2195
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-
Mikhailopulo, I.A.1
Poopeiko, N.E.2
Pricota, T.I.3
Sivets, G.G.4
Kvasyuk, E.I.5
Balzarini, J.6
De Clercq, E.7
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31
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85031154839
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note
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3CN) δ 153.8 and 151.2.
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-
-
-
32
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0038230095
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Sørensen M.D., Kværnø L., Bryld T., Håkansson A.E., Verbeure B., Gaubert G., Herdewijn P., Wengel J. J. Am. Chem. Soc. 124:2002;2164.
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(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 2164
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-
Sørensen, M.D.1
Kværnø, L.2
Bryld, T.3
Håkansson, A.E.4
Verbeure, B.5
Gaubert, G.6
Herdewijn, P.7
Wengel, J.8
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33
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85031156881
-
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note
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2SO)) δ 164.10, 154.18 (q, J=37.4 Hz), 150.02, 136.78, 115.75 (q, J=287.3 Hz), 106.13, 89.22, 87.88, 72.30, 60.82, 57.12, 53.19, 12.50.
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-
-
-
34
-
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85031149098
-
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note
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3CN) δ 154.9, 154.2, 152.5, 152.3.
-
-
-
-
39
-
-
85031146995
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-
note
-
-; found/calcd) ON4, 2776/2778; ON6, 2833/2833; ON7, 2834/2834; ON9, 4191/4197; ON10, 4210/4215; ON11, 4220/4221; ON12, 4191/4197; ON14, 4247/4251; ON15, 4300/4302.
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-
-
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41
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85031152057
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note
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Hybridization was performed in 100 mM NaCl, 10 mM KCl, 20 mM Tris-HCl (pH 7.5) by heating to 65°C, slowly cooling after 2 min to 37°C followed by incubation at 5°C for 1-2 h. The resulting complexes were then analyzed on 20% acrylamide gels run at approximately 14°C.
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