A Practical Synthesis of Nonpeptide Cyclic Ureas as Potent HIV Protease Inhibitors
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Cited by 23 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Transition metal-catalyzed oxidative carbonylation of amines to ureas;EUR J ORG CHEM;2007
2. Diastereoselective Ethynylation of Chiral α-(Dibenzylamino) Aldehydes: Synthesis ofmeso- and HomochiralC2-Symmetrical 1,6-Diamino-2,5-diols;European Journal of Organic Chemistry;2006-08
3. Thiazole-Mediated Synthetic Methodology;Chemical Reviews;2004-02-14
4. Synthesis of Seven-Membered Ring Diazepin-2-ones via Palladium-Catalyzed Highly Regioselective Cyclization of 2-Vinylpyrrolidines with Aryl Isocyanates;The Journal of Organic Chemistry;2003-03-28
5. Synthesis, antiviral activity and pharmacokinetics of P1/P1′ substituted 3-aminoindazole cyclic urea HIV protease inhibitors;Bioorganic & Medicinal Chemistry Letters;2003-02
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