## Abstract The MKC‐442 analogue 6‐(3,5‐dimethylbenzyl)‐5‐ethyluracil substituted with a (propargyloxo)methyl group at N(1) has previously been found highly active against HIV‐1. The CC bond in the substituent at N(1) is here utilized in a series of chemical reactions in order to develop new agent
Synthesis and Anti-HIV-1 Activity of New MKC-442 Analogues with an Alkynyl-Substituted 6-Benzyl Group*
✍ Scribed by Youssef L. Aly; Erik B. Pedersen; Paolo La Colla; Roberta Loddo
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 714 KB
- Volume
- 340
- Category
- Article
- ISSN
- 0365-6233
No coin nor oath required. For personal study only.
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