Increasing the Structural Span of Alkyne Metathesis. Issue 39 (3rd September 2013)

• Record Type: Journal Article
• Authors: Persich, Peter; Llaveria, Josep; Lhermet, Rudy; de Haro, Teresa; Stade, Robert; Kondoh, Azusa; Fürstner, Alois
• Is Part Of: Chemistry. Volume 19:Issue 39(2013)
• Page Start: 13047
• Page End: 13058
• Publication Date: 2013-09-03
• Subjects: Chemistry -- Periodicals; 540
• DOI: 10.1002/chem.201302320
• Languages: English
• ISSNs: 0947-6539

Abstract

<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>A new generation of alkyne metathesis catalysts, which are distinguished by high activity and an exquisite functional group tolerance, allows the scope of this transformation to be extended beyond its traditional range. They accept substrates that were previously found problematic or unreactive, such as propargyl alcohol derivatives, electron‐deficient and electron‐rich acetylenes of various types, and even terminal alkynes. Moreover, post‐metathetic transformations other than semi‐reduction increase the structural portfolio, as witnessed by the synthesis of a annulated phenol derivative via ring‐closing alkyne metathesis (RCAM) followed by a transannular gold‐catalyzed Conia‐ene reaction. Further examples encompass a post‐metathetic transannular ketone–alkyne cyclization with formation of a trisubstituted furan, a ruthenium‐catalyzed redox isomerization, and a Meyer–Schuster rearrangement/oxa‐Michael cascade. These reaction modes fueled model studies toward salicylate macrolides, furanocembranolides, and the cytotoxic macrolides acutiphycin and enigmazole A; moreover, they served as the key design elements of concise total syntheses of dehydrocurvularin (<bold>27</bold>) and the antibiotic agent A26771B (<bold>36</bold>).</p> </abstract>