Stereoselective synthesis of tetrahydropyran and oxepane systems by the endo-cyclization of hydroxy styrylepoxides
- 1 August 1997
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 38 (31) , 5545-5548
- https://doi.org/10.1016/s0040-4039(97)01197-0
Abstract
No abstract availableThis publication has 17 references indexed in Scilit:
- Enantioselective synthesis of medium-ring sub-units of brevetoxin A by ring-closing metathesisTetrahedron Letters, 1997
- Synthesis of brevetoxin sub-units by sequential ring-closing metathesis and hydroborationTetrahedron Letters, 1997
- Stereoselective synthesis of six- and seven-membered ether rings based on the ring expansionTetrahedron Letters, 1996
- Useful Designs in the Synthesis of Trans-Fused Polyether ToxinsChemical Reviews, 1995
- Activation of 7-endo over 6-exo epoxide openings. Synthesis of oxepane and tetrahydropyran systemsJournal of the American Chemical Society, 1989
- Activation of 6-endo over 5-exo hydroxy epoxide openings. Stereoselective and ring selective synthesis of tetrahydrofuran and tetrahydropyran systemsJournal of the American Chemical Society, 1989
- Pd catalyzed chemoselective cyclization to cyclic ethersTetrahedron Letters, 1988
- Activation of 6-endo over 5-exo epoxide openings. Ring-selective formation of tetrahydropyran systems and stereocontrolled synthesis of the ABC ring framework of brevetoxin BJournal of the Chemical Society, Chemical Communications, 1985
- Isolation and structure of brevetoxin B from the "red tide" dinoflagellate Ptychodiscus brevis (Gymnodinium breve)Journal of the American Chemical Society, 1981
- Rules for ring closureJournal of the Chemical Society, Chemical Communications, 1976