-
3
-
-
0028905177
-
-
and references cited herein
-
Ford H. Jr., Siddiqui M.A., Driscoll J.S., Marquez V.E., Kelley J.A., Mitsuya H., Shirasaka T. J. Med. Chem. 38:1995;1189-1195. and references cited herein.
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(1995)
J. Med. Chem.
, vol.38
, pp. 1189-1195
-
-
Ford H., Jr.1
Siddiqui, M.A.2
Driscoll, J.S.3
Marquez, V.E.4
Kelley, J.A.5
Mitsuya, H.6
Shirasaka, T.7
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5
-
-
0342950138
-
-
In a different synthetic approach, we started from inosine 2 and unsuccessfully tried to prepare the classical 2′,3′-O-(methoxymethylene) derivative that was needed for further elaboration. Due to insolubility of 2 in the reaction medium, poor yields of the required compound were obtained using trimethylorthoformate as reagent and solvent, whereas addition of DMSO or DMF improved the yields but complicated the work-up.
-
In a different synthetic approach, we started from inosine 2 and unsuccessfully tried to prepare the classical 2′,3′-O-(methoxymethylene) derivative that was needed for further elaboration. Due to insolubility of 2 in the reaction medium, poor yields of the required compound were obtained using trimethylorthoformate as reagent and solvent, whereas addition of DMSO or DMF improved the yields but complicated the work-up.
-
-
-
-
7
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-
0015785131
-
-
For another preparation of 3′-deoxyinosine 6 see
-
For another preparation of 3′-deoxyinosine 6 see: Yamazaki, A.; Akiyama, M.; Kumashiro, I.; Ikehara, M. Chem. Pharm. Bull. 1973, 21, 1143-1146.
-
(1973)
Chem. Pharm. Bull.
, vol.21
, pp. 1143-1146
-
-
Yamazaki, A.1
Akiyama, M.2
Kumashiro, I.3
Ikehara, M.4
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8
-
-
0029914055
-
-
A few data on the biological effects of the nucleoside have been recently reported; see
-
A few data on the biological effects of the nucleoside have been recently reported; see: Nakajima-Shimada, J.; Hirota, Y.; Aoki, T. Antimicrob. Agents Chemother. 1996, 40, 2455-2458.
-
(1996)
Antimicrob. Agents Chemother.
, vol.40
, pp. 2455-2458
-
-
Nakajima-Shimada, J.1
Hirota, Y.2
Aoki, T.3
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10
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-
0000404890
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-
(a)
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(a) Degueil-Castaing, M.; De Jeso, B.; Drouillard, S.; Maillard, B. Tetrahedron Lett. 1987, 28, 953-954.
-
(1987)
Tetrahedron Lett.
, vol.28
, pp. 953-954
-
-
Degueil-Castaing, M.1
De Jeso, B.2
Drouillard, S.3
Maillard, B.4
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11
-
-
33845279035
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-
(b)
-
(b) Wang, Y.-F.; Lalonde, J. J.; Momongan, M.; Bergbreiter, D. E.; Wong, C.-H. J. Am. Chem. Soc. 1988, 110, 7200-7205.
-
(1988)
J. Am. Chem. Soc.
, vol.110
, pp. 7200-7205
-
-
Wang, Y.-F.1
Lalonde, J.J.2
Momongan, M.3
Bergbreiter, D.E.4
Wong, C.-H.5
-
13
-
-
0343385551
-
-
Longer reaction time and/or higher temperatures led to appearance of 5′-substituted and disubstituted compounds.
-
Longer reaction time and/or higher temperatures led to appearance of 5′-substituted and disubstituted compounds.
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-
-
-
14
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0030020948
-
-
Marrone T.J., Straatsma T.P., Briggs J.M., Wilson D.K., Quiocho F.A., McCammon J.A.J. Med. Chem. 39:1996;277-284.
-
(1996)
Med. Chem.
, vol.39
, pp. 277-284
-
-
Marrone, T.J.1
Straatsma, T.P.2
Briggs, J.M.3
Wilson, D.K.4
Quiocho, F.A.5
McCammon, J.A.J.6
-
15
-
-
0031013663
-
-
Recent observations on the importance of the same hydroxy group, in a carbocyclic nucleoside (Neplanocin A) on the ADA-catalyzed deamination have been reported; see
-
Recent observations on the importance of the same hydroxy group, in a carbocyclic nucleoside (Neplanocin A) on the ADA-catalyzed deamination have been reported; see: Shuto, S.; Obara, T.; Yaginuma, S.; Matsuda, A. Chem. Pharm. Bull. 1997, 45, 138-142.
-
(1997)
Chem. Pharm. Bull.
, vol.45
, pp. 138-142
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-
Shuto, S.1
Obara, T.2
Yaginuma, S.3
Matsuda, A.4
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23
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0342950134
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Wnuk S.F., Yuan C.-S., Borchardt R.T., Balzarini J., De Clercq E., Robins M.J. J. Med. Chem. 40:1997;1609-1618.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 1609-1618
-
-
Wnuk, S.F.1
Yuan, C.-S.2
Borchardt, R.T.3
Balzarini, J.4
De Clercq, E.5
Robins, M.J.6
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