Total Synthesis and Stereochemical Assignment of Myriaporones 1, 3, and 4
- 17 March 2004
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 43 (13) , 1728-1730
- https://doi.org/10.1002/anie.200353348
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Index: Angew. Chem. Int. Ed. 2004Angewandte Chemie International Edition in English, 2004
- Total Synthesis of Natural MyriaporonesAngewandte Chemie, 2004
- Total Synthesis of (+)-13-DeoxytedanolideJournal of the American Chemical Society, 2002
- Synthetic Studies of an 18-Membered Antitumor Macrolide, Tedanolide. 6. Synthesis of a Key Intermediate via a Highly Efficient Macrolactonization of Computer-Aid Designed Seco-Acid.CHEMICAL & PHARMACEUTICAL BULLETIN, 2000
- Studies on the Synthesis of Tedanolide: Synthesis of the C(5)−C(21) Segment via a Highly Stereoselective Fragment Assembly Aldol Reaction of a Chiral β,γ-Unsaturated Methyl KetoneOrganic Letters, 1999
- Tris(dimethylamino)sulfonium Difluorotrimethylsilicate, a Mild Reagent for the Removal of Silicon Protecting GroupsThe Journal of Organic Chemistry, 1998
- The 1994 Japan-U.S. Seminar on Bioorganic Marine Chemistry, Meeting ReportJournal of Natural Products, 1995
- A mild oxidizing reagent for alcohols and 1,2-diols: o-Iodoxybenzoic acid (IBX) in DMSOTetrahedron Letters, 1994
- Ring Cleavage of 3,5-Disubstituted 2-lsoxazolines by Molybdenum Hexacarbonyl and Water to β-Hydroxy KetonesSynthesis, 1987
- Readily accessible 12-I-5 oxidant for the conversion of primary and secondary alcohols to aldehydes and ketonesThe Journal of Organic Chemistry, 1983