REGIOSELECTIVITY IN THE LITHIATION OF URIDINE. EFFECT OF THE SUGAR PROTECTING GROUPS
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Reference12 articles.
1. “Umpulong” of reactivity at the C-6 position of uridine: a simple and general method for 6-substituted uridines
2. A simplified synthesis of 8-substituted purine nucleosides via lithiation of 6-chloro-9-(2,3-O-isopropylidene-.BETA.-D-ribofuranosyl)purine.
3. Lithiation of 5,6-dihydrouridine: a new route to 5-substituted uridines
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