Article ID Journal Published Year Pages File Type
5284449 Tetrahedron Letters 2005 4 Pages PDF
Abstract
The hydroquinone lactone core of the floresolides was synthesized through a ring-closing metathesis (RCM) approach. Optimal RCM efficiency was obtained at higher reaction concentration. An unexpected Lewis acid-promoted rearrangement of the hydroquinone is also discussed.
Keywords
Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
Preview
Synthesis of the floresolide B hydroquinone lactone core using ring-closing metathesis
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