The 3-Deaza and 7-Deaza Derivatives of 5'-Amino-5'-deoxy-5'-noraristeromycin
2006 ◽
Vol 71
(7)
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pp. 1122-1129
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Keyword(s):
B Virus
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The 3-deaza and 7-deaza derivatives of 5'-amino-5'-deoxy-5'-noraristeromycin (6 and 7, respectively) have been prepared from the common starting material (+)-(1R,4S)-4-hydroxycyclopent-2-en-1-yl acetate (8). Two Pd(0)-catalyzed allylic substitution reactions afforded the desired azide intermediates, 12 and 16, which were transformed to target compounds by standard procedures. These compounds were evaluated against a large number of viruses and found to be inactive except for weak effect against hepatitis B virus: 6, EC50 4.7 μM (3TC EC50 0.056 μM); 7, EC50 4.8 μM (3TC EC50 0.063 μM).
2011 ◽
Vol 21
(7)
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pp. 1179-1187
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2003 ◽
Vol 2003
(1)
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pp. 2-3
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1989 ◽
Vol 42
(4)
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pp. 644-646
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1999 ◽
Vol 40
(3)
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pp. 167-178
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