Stereoselective Synthesis of the Chiral Tetrahydropyrane Core of Swinholides and Misakinolides
- 1 July 1999
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 28 (7) , 601-602
- https://doi.org/10.1246/cl.1999.601
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- The total synthesis of swinholide A. Part 1: A stereocontrolled synthesis of a C19-C32 segmentTetrahedron, 1995
- The total synthesis of swinholide A. Part 2: A stereocontrolled synthesis of a c1–c15 segmentTetrahedron, 1995
- Synthetic study of marine macrolide swinholide A. stereocontrolled synthesis of the C11 - C23 segmentTetrahedron Letters, 1994
- Total Synthesis of Swinholide A and Hemiswinholide AJournal of the American Chemical Society, 1994
- Synthetic Study of Marine Macrolide Swinholide A. Stereocontrolled Synthesis of the C11-C32 Segment.CHEMICAL & PHARMACEUTICAL BULLETIN, 1994
- Molecular conformation of swinholide A, a potent cytotoxic dimeric macrolide from the Okinawan marine sponge Theonella swinhoei: x-ray crystal structure of its diketone derivativeThe Journal of Organic Chemistry, 1991
- Absolute stereostructure of swinholide A, a potent cytotoxic macrolide from the Okinawan marine sponge Theonella swinhoeiJournal of the American Chemical Society, 1990
- Marine natural products. XXIV. The absolute stereostructure of misakinolide A, a potent cytotoxic dimeric macrolide from an Okinawan marine sponge Theonella sp.CHEMICAL & PHARMACEUTICAL BULLETIN, 1990
- Structure of swinholide A, a potent cytotoxic macrolide from the Okinawan marine spongeTetrahedron Letters, 1989
- Structure of swinholide-a, a new macrolide from the marine spongeTetrahedron Letters, 1985