-
2
-
-
0003098462
-
-
Crook, S. T., Lebleu, B., Eds.; CRC Press: Boca Raton, FL
-
(b) Cook, P. D. In Antisense Research and Applications; Crook, S. T., Lebleu, B., Eds.; CRC Press: Boca Raton, FL, 1993; pp 149-187.
-
(1993)
Antisense Research and Applications
, pp. 149-187
-
-
Cook, P.D.1
-
3
-
-
0345706517
-
-
De Mesmaeker, A.; Haener, R.; Martin, P.; Moser, H. E. Acc. Chem. Res. 1995, 28, 366.
-
(1995)
Acc. Chem. Res.
, vol.28
, pp. 366
-
-
De Mesmaeker, A.1
Haener, R.2
Martin, P.3
Moser, H.E.4
-
8
-
-
0030053079
-
-
Morvan, F.; Sanghvi, Y. S.; Perbost, M.; Vasseur, J.-J.; Bellon, L. J. Am. Chem. Soc. 1996, 118, 255.
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 255
-
-
Morvan, F.1
Sanghvi, Y.S.2
Perbost, M.3
Vasseur, J.-J.4
Bellon, L.5
-
9
-
-
0030484689
-
-
De Mesmaeker, A.; Lesueur, C.; Bevierre, M.-O.; Waldner, A.; Fritsch, V.; Wolf, R. M. Angew. Chem., Int. Ed. Engl. 1996, 35, 2790.
-
(1996)
Angew. Chem., Int. Ed. Engl.
, vol.35
, pp. 2790
-
-
De Mesmaeker, A.1
Lesueur, C.2
Bevierre, M.-O.3
Waldner, A.4
Fritsch, V.5
Wolf, R.M.6
-
10
-
-
0029160308
-
-
(a) Bohler, C.; Nielsen, P. E.; Orgel, L. E. Nature 1995, 376, 578.
-
(1995)
Nature
, vol.376
, pp. 578
-
-
Bohler, C.1
Nielsen, P.E.2
Orgel, L.E.3
-
11
-
-
13344293719
-
-
(b) Veselkov, A. G.; Demidov, V. V.; Frank-Kamenetiskii, N. D.; Nielsen, P. E. Nature 1996, 379, 214.
-
(1996)
Nature
, vol.379
, pp. 214
-
-
Veselkov, A.G.1
Demidov, V.V.2
Frank-Kamenetiskii, N.D.3
Nielsen, P.E.4
-
12
-
-
0032476790
-
-
Uhlmann, E.; Peyman, A.; Breipohl, G.; Will, D. W. Angew. Chem., Int. Ed. 1998, 37, 2796.
-
(1998)
Angew. Chem., Int. Ed.
, vol.37
, pp. 2796
-
-
Uhlmann, E.1
Peyman, A.2
Breipohl, G.3
Will, D.W.4
-
13
-
-
0038882443
-
-
(a) Barawkar, D. A.; Rajeev, K. G.; Kumar, V. A.; Ganesh, K. N. Nucleic Acid Res. 1998, 26, 566.
-
(1998)
Nucleic Acid Res.
, vol.26
, pp. 566
-
-
Barawkar, D.A.1
Rajeev, K.G.2
Kumar, V.A.3
Ganesh, K.N.4
-
14
-
-
0031972931
-
-
(b) Ueno, Y.; Mikawa, M.; Matsuda, A. Bioconjugate Chem. 1998, 9, 33.
-
(1998)
Bioconjugate Chem.
, vol.9
, pp. 33
-
-
Ueno, Y.1
Mikawa, M.2
Matsuda, A.3
-
15
-
-
0001191968
-
-
Ueno, Y.; Nagasawa, Y.; Sugimoto, I.; Kojima, N.; Kanazaki, M.; Shuto, S.; Matsuda, A. J. Org. Chem. 1998, 63, 1660.
-
(1998)
J. Org. Chem.
, vol.63
, pp. 1660
-
-
Ueno, Y.1
Nagasawa, Y.2
Sugimoto, I.3
Kojima, N.4
Kanazaki, M.5
Shuto, S.6
Matsuda, A.7
-
16
-
-
0028307714
-
-
Jung, P. M.; Histand, G.; Letsinger, R. L. Nucleosides Nucleotides 1994, 13, 1597.
-
(1994)
Nucleosides Nucleotides
, vol.13
, pp. 1597
-
-
Jung, P.M.1
Histand, G.2
Letsinger, R.L.3
-
17
-
-
0028059256
-
-
(a) Dempcy, R. O.; Almarsson, O.; Bruice, T. C. Proc. Natl. Acad. Sci. U.S.A. 1994, 91, 7864.
-
(1994)
Proc. Natl. Acad. Sci. U.S.A.
, vol.91
, pp. 7864
-
-
Dempcy, R.O.1
Almarsson, O.2
Bruice, T.C.3
-
18
-
-
0029001386
-
-
(b) Dempcy, R. O.; Browne, K. A.; Bruice, T. C. J. Am. Chem. Soc. 1995, 117, 6140.
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 6140
-
-
Dempcy, R.O.1
Browne, K.A.2
Bruice, T.C.3
-
19
-
-
0029036905
-
-
Dempcy, R. O.; Browne, K. A.; Bruice, T. C. Proc. Natl. Acad. Sci. U.S.A. 1995, 92, 6097.
-
(1995)
Proc. Natl. Acad. Sci. U.S.A.
, vol.92
, pp. 6097
-
-
Dempcy, R.O.1
Browne, K.A.2
Bruice, T.C.3
-
20
-
-
0033612014
-
-
Linkletter, B. A.; Szabo, I. E.; Bruice, T. C. J. Am. Chem. Soc. 1999, 121, 3888.
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 3888
-
-
Linkletter, B.A.1
Szabo, I.E.2
Bruice, T.C.3
-
21
-
-
0029935167
-
-
Synthesis of tetrameric adenosyl RNG in the solution phase has already been reported: Dempcy, R. O.; Luo, J.; Bruice, T. C. Proc. Natl. Acad. Sci. U.S.A. 1996, 93, 4326.
-
(1996)
Proc. Natl. Acad. Sci. U.S.A.
, vol.93
, pp. 4326
-
-
Dempcy, R.O.1
Luo, J.2
Bruice, T.C.3
-
22
-
-
0032537616
-
-
Barawkar, D. A.; Linkletter, B. A.; Bruice, T. C. Bioorg. Med. Chem. Lett. 1998, 8, 1517.
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, pp. 1517
-
-
Barawkar, D.A.1
Linkletter, B.A.2
Bruice, T.C.3
-
23
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-
0040660411
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note
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4OH treatment. We have also tried some acyl groups for the N-protection of thiourea. In these cases, reaction of N-acyl isothiocyanate with 3′-amino nucleoside gave not only desired 3′-thiourea nucleoside but also 3′-N-acylated nucleoside as a side product. Formation of N-acyl compound was increased with the increase of electronegativity of the acyl group on isothiocyanate.
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0032480993
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Ogawa, A.; Tanaka, M.; Sasaki, T.; Matsuda, A. J. Med. Chem. 1998, 41, 5094.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 5094
-
-
Ogawa, A.1
Tanaka, M.2
Sasaki, T.3
Matsuda, A.4
-
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0040066894
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note
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+ 911.3510.
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27
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85088882916
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note
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2+ 657.2] form was observed.
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