Synthesis and HIV-1 integrase inhibitory activities of caffeic acid dimers derived from Salvia officinalis
- 15 November 2005
- journal article
- research article
- Published by Elsevier BV in Bioorganic & Medicinal Chemistry Letters
- Vol. 15 (22), 5053-5056
- https://doi.org/10.1016/j.bmcl.2005.07.091
Abstract
No abstract availableKeywords
This publication has 44 references indexed in Scilit:
- Peptide Inhibitors of HIV-1 Integrase Dissociate the Enzyme OligomersBiochemistry, 2001
- Four New Caffeic Acid Metabolites, Yunnaneic Acids E-H, from Salvia yunnanensis.CHEMICAL & PHARMACEUTICAL BULLETIN, 1997
- Synthetic approaches toward ecteinascidins. Part 1. Preparation of an (E)-2-arylidene-3-benzyl-1,5-imino-3-benzazocin-4-one having a protected phenol in the E-ringJournal of the Chemical Society, Perkin Transactions 1, 1997
- Some fatty acids having anO-heterocycle in their terminal positions.II. ω-(3-Coumarinyl)alkanoic acids and ω-(2-chromonyl)alkanoic acidsJournal of Heterocyclic Chemistry, 1991
- Synthesis of 3-(3-Benzofuranyl)coumarinsSynthetic Communications, 1990
- Magnesium and ammonium-potassium lithospermates B, the active principles having a uremia-preventive effect from Salvia miltiorrhiza.CHEMICAL & PHARMACEUTICAL BULLETIN, 1989
- Synthesis of New Heterocycles, Part II: Synthesis of New Benzopyranobenzoxazinone Ring System Involving a Novel RearrangementSynthetic Communications, 1987
- Synthesis of a New Benzopyranobenzoxazine Ring SystemSynthetic Communications, 1987
- A General Synthesis of Bis[coumarinyl] Ethers: Synthesis of Daphnoretin Methyl EtherSynthesis, 1986
- General Synthesis of 3-PhenoxycoumarinsSynthesis, 1985