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0024687658
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37
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0000178356
-
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1,3,5-Tri-O-acetyl-2-deoxy-D-ribofuranose was prepared via a multi-step synthesis according to the following procedures: (a) Recondo, E. F.; Rinderknecht, G. L. Helv. Chim. Acta 1959, 42, 1171-1173; (b) Kline, P. C.; Serianni, A. S. J. Am. Chem. Soc. 1990, 112, 7373-7381; (c) Bhat, C. C. In Synthetic Procedures in Nucleic Acids Chemistry: Vol. 1; Zorbach, W. W.; Tipson, R. S., Eds.; John Wiley and Sons: New York, 1968; pp. 521-522; (d) Gold, A.; Sangaiah, R. Nucleosides & Nucleotides 1990, 9, 907-912.
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Recondo, E.F.1
Rinderknecht, G.L.2
-
38
-
-
0025154975
-
-
1,3,5-Tri-O-acetyl-2-deoxy-D-ribofuranose was prepared via a multi-step synthesis according to the following procedures: (a) Recondo, E. F.; Rinderknecht, G. L. Helv. Chim. Acta 1959, 42, 1171-1173; (b) Kline, P. C.; Serianni, A. S. J. Am. Chem. Soc. 1990, 112, 7373-7381; (c) Bhat, C. C. In Synthetic Procedures in Nucleic Acids Chemistry: Vol. 1; Zorbach, W. W.; Tipson, R. S., Eds.; John Wiley and Sons: New York, 1968; pp. 521-522; (d) Gold, A.; Sangaiah, R. Nucleosides & Nucleotides 1990, 9, 907-912.
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Kline, P.C.1
Serianni, A.S.2
-
39
-
-
0000416466
-
-
Zorbach W. W.; Tipson, R. S., Eds.; John Wiley and Sons: New York
-
1,3,5-Tri-O-acetyl-2-deoxy-D-ribofuranose was prepared via a multi-step synthesis according to the following procedures: (a) Recondo, E. F.; Rinderknecht, G. L. Helv. Chim. Acta 1959, 42, 1171-1173; (b) Kline, P. C.; Serianni, A. S. J. Am. Chem. Soc. 1990, 112, 7373-7381; (c) Bhat, C. C. In Synthetic Procedures in Nucleic Acids Chemistry: Vol. 1; Zorbach, W. W.; Tipson, R. S., Eds.; John Wiley and Sons: New York, 1968; pp. 521-522; (d) Gold, A.; Sangaiah, R. Nucleosides & Nucleotides 1990, 9, 907-912.
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(1968)
Synthetic Procedures in Nucleic Acids Chemistry: Vol. 1
, vol.1
, pp. 521-522
-
-
Bhat, C.C.1
-
40
-
-
0025696516
-
-
1,3,5-Tri-O-acetyl-2-deoxy-D-ribofuranose was prepared via a multi-step synthesis according to the following procedures: (a) Recondo, E. F.; Rinderknecht, G. L. Helv. Chim. Acta 1959, 42, 1171-1173; (b) Kline, P. C.; Serianni, A. S. J. Am. Chem. Soc. 1990, 112, 7373-7381; (c) Bhat, C. C. In Synthetic Procedures in Nucleic Acids Chemistry: Vol. 1; Zorbach, W. W.; Tipson, R. S., Eds.; John Wiley and Sons: New York, 1968; pp. 521-522; (d) Gold, A.; Sangaiah, R. Nucleosides & Nucleotides 1990, 9, 907-912.
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Gold, A.1
Sangaiah, R.2
-
41
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-
84981759555
-
-
Hoffer M. Chem. Ber. 93:1960;2777-2781.
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, vol.93
, pp. 2777-2781
-
-
Hoffer, M.1
-
50
-
-
0012993637
-
-
+
-
+.
-
-
-
-
51
-
-
0012983049
-
-
+
-
+.
-
-
-
-
54
-
-
33748973394
-
-
3), 3.93-3.98 (m, 2 H, H-4), 4.17-4.29 (m, 1 H, H-3), 5.49 (s, 1 H, Ph-CH), 7.27-7.58 ppm (m, 5 H, aromatic H).
-
(1996)
Liebigs Ann.
, pp. 2135-2140
-
-
Blechert, S.1
Dollt, H.2
-
56
-
-
0012936208
-
-
3): d=1.58-1.63, 1.79-1.81 (m, 2 H, H-5), 2.50-2.77 (m, 2 H, H-2), 3.90-3.94 (m, 1 H, H-4), 3.95-3.99 (m, 1 H, H-4), 4.20-4.30 (m, 1 H, H-3), 5.50 (s, 1 H, Ph-CH), 7.27-7.56 ppm (m, 5 H, aromatic H)
-
3): d=1.58-1.63, 1.79-1.81 (m, 2 H, H-5), 2.50-2.77 (m, 2 H, H-2), 3.90-3.94 (m, 1 H, H-4), 3.95-3.99 (m, 1 H, H-4), 4.20-4.30 (m, 1 H, H-3), 5.50 (s, 1 H, Ph-CH), 7.27-7.56 ppm (m, 5 H, aromatic H).
-
-
-
-
58
-
-
0012933918
-
-
The pale yellow solid of 11 was used directly without characterization
-
The pale yellow solid of 11 was used directly without characterization.
-
-
-
-
59
-
-
0012942221
-
-
note
-
+.
-
-
-
-
61
-
-
0012989602
-
-
note
-
+.
-
-
-
-
62
-
-
0013021887
-
-
max=213, 284, 431 nm)
-
max=213, 284, 431 nm).
-
-
-
|