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Synthesis of base-modified dihydropacidamycins
Rémy C Lemoine1, Angela Magon, Scott J Hecker
1Essential Therapeutics, Inc., 850Maude Avenue, Mountain View, CA 94043, USA. rlemoine@etrx.com
Bioorganic & Medicinal Chemistry Letters
|March 23, 2002
Abstract:
We describe in this paper the synthesis of 1,2-di-O-acetyl-5-azido-3,5-dideoxy-alpha,beta-L-arabinofuranose, a carbohydrate donor that was used for the synthesis of 1-(5'-amino-3',5'-dideoxy-alpha-L-arabinofuranosyl)uracil, the nucleoside found in dihydropacidamycin D. The carbohydrate donor was also used for the synthesis of a set of new nucleosides that were introduced in new dihydropacidamycins. These compounds were tested for biological activity, and the results showed that uracil is the only base recognized by MraY.