Resolution of 9-(c-4,t-5-bishydroxymethylcyclopent-2-en-r-1-yl)-9H-adenine and selective inhibition of human immunodeficiency virus by the (−) enantiomer
- 1 April 1992
- journal article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 184 (1), 154-159
- https://doi.org/10.1016/0006-291x(92)91172-m
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Synthesis and antiviral activity of enantiomeric forms of cyclobutyl nucleoside analogsJournal of Medicinal Chemistry, 1991
- Synthesis of Nucleosides and Related Compounds. XXII. Carbocyclic Analogues of Thymidine and Related Compounds from 2-Azabicyclo(2.2.1)hept-5-en-3-ones.CHEMICAL & PHARMACEUTICAL BULLETIN, 1991
- Synthesis of Nucleosides and Related Compounds. Part XX. Synthesis of Carbocyclic Nucleosides from 2-Azabicyclo(2.2.1)hept-5-en-3-ones: Sodium Borohydride-Mediated Carbon-Nitrogen Bond Cleavage of Five-and Six-Membered Lactams.CHEMICAL & PHARMACEUTICAL BULLETIN, 1991
- Resolution of racemic carbovir and selective inhibition of human immunodeficiency virus by the (−) enantiomerBiochemical and Biophysical Research Communications, 1990
- New Soluble-Formazan Assay for HIV-1 Cytopathic Effects: Application to High-Flux Screening of Synthetic and Natural Products for AIDS-Antiviral ActivityJNCI Journal of the National Cancer Institute, 1989
- A new method for the highly stereoselective synthesis of nucleosides. Creation of new dienophiles and use of reductive retrograde aldol reaction.Journal of Synthetic Organic Chemistry, Japan, 1989
- Frequent Detection and Isolation of Cytopathic Retroviruses (HTLV-III) from Patients with AIDS and at Risk for AIDSScience, 1984