Evolution of anti-HIV drug candidates. Part 3: diarylpyrimidine (DAPY) analogues

This publication has 15 references indexed in Scilit:

• Evolution of anti-HIV drug candidates. Part 1: From α-Anilinophenylacetamide (α-APA) to imidoyl thiourea (ITU)
  Bioorganic & Medicinal Chemistry Letters, 2001
• The role of non-nucleoside reverse transcriptase inhibitors (NNRTIs) in the therapy of HIV-1 infection1Presented at the Eleventh International Conference on Antiviral Research, San Diego, CA, 5–10 April 1998.1
  Antiviral Research, 1998
• Efavirenz
  Drugs of the Future, 1998
• Unusual sensitivity to the concentration of ethanol in the boron trifluoride/ethanol‐catalyzed synthesis of 5,10,15,20‐tetrakis‐(4‐cyano‐2,6‐dimethylphenyl)porphyrin by the lindsey method
  Journal of Heterocyclic Chemistry, 1997
• A new route to 1,5-disubstituted 4-arylsulfonylpyrazoles by lithiation of 1-methyl-4-arylsulfonylpyrazoles
  Tetrahedron, 1995
• Structure of HIV-1 RT/TIBO R 86183 complex reveals similarity in the binding of diverse nonnucleoside inhibitors
  Nature Structural & Molecular Biology, 1995
• Condensed Heteroaromatic Ring Systems. XXI. Synthesis of Pyrrolo(2,3-d)pyrimidines and Pyrrolo(3,2-d)pyrimidines.
  CHEMICAL & PHARMACEUTICAL BULLETIN, 1993
• Inhibition of HIV-1 Replication by a Nonnucleoside Reverse Transcriptase Inhibitor
  Science, 1990
• A Facile Synthesis of Ethynyl-Substituted Six-MemberedN-Heteroaromatic Compounds
  Synthesis, 1983
• Heterocyclic series. X. 1,3,9-Triazaphenothiazine ring system, a new phenothiazine ring
  The Journal of Organic Chemistry, 1975