Abstract
Stereoselective synthesis of the optically pure tetrahydropyrane core of swinholides and misakinolide A starting from (S)-methyl lactate is described in which the highly stereoselective intramolecular iodoetherification for construction of the tetrahydropyrane ring and the regioselective ring-opening reaction of an epoxide are involved as key steps.
Original language | English |
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Pages (from-to) | 601-602 |
Number of pages | 2 |
Journal | Chemistry Letters |
Issue number | 7 |
DOIs | |
State | Published - 1999 |
ASJC Scopus subject areas
- General Chemistry