Ring-closing metathesis strategy to unsaturated γ- and δ-lactones: Synthesis of hydroxyethylene isostere for protease inhibitors
- 1 June 1998
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 39 (26) , 4651-4654
- https://doi.org/10.1016/s0040-4039(98)00887-9
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- Olefin Metathesis in Organic ChemistryAngewandte Chemie International Edition in English, 1997
- Total Syntheses of (+)-Ricinelaidic Acid Lactone and of (−)-Gloeosporone Based on Transition-Metal-Catalyzed C−C Bond FormationsJournal of the American Chemical Society, 1997
- Total Syntheses of Epothilones A and BJournal of the American Chemical Society, 1997
- Conformational Bias by a Removable Substituent. Synthesis of Eight-Membered Cyclic Ethers via Ring-Closing MetathesisJournal of the American Chemical Society, 1997
- Synthesis of epothilones A and B in solid and solution phaseNature, 1997
- Conformationally Unbiased Macrocyclization Reactions by Ring Closing MetathesisThe Journal of Organic Chemistry, 1996
- Catalytic and Enantioselective Route to Medium-Ring Heterocycles. Asymmetric Zirconium-Catalyzed Ethylmagnesation of Seven- and Eight-Membered RingsJournal of the American Chemical Society, 1996
- Ring-Closing Metathesis and Related Processes in Organic SynthesisAccounts of Chemical Research, 1995
- Cascade Catalysis in Synthesis. An Enantioselective Route to Sch 38516 (and Fluvirucin B1) Aglycon MacrolactamJournal of the American Chemical Society, 1995
- Syntheses and activities of new single-component, ruthenium-based olefin metathesis catalystsJournal of the American Chemical Society, 1993