Synthesis of oxylipids via a boronic ester cycloetherification approach

2025/01/01 by Markus Tost, Uli Kazmaier · 1 voice
Chemistry · #Asymmetric Hydrogenation and Catalysis #Asymmetric Synthesis and Catalysis #Chemical Synthesis and Reactions

paper · doi:10.1039/d5qo00213c

openalex publication_date 2025/01/01 · openalex created_date 2025/03/09 · openalex updated_date 2026/07/25

Abstract

Matteson homologation using trimethylsilylethanol as a nucleophile is perfectly suited for the synthesis of oxylipids, since this silyl protecting group is automatically cleaved to generate substituted tetrahydrofuran rings.

Citations

• Asymmetric Synthesis of the Four Stereoisomers of 4-Methyl-3-heptanol via Boronic Esters: Sequential Double Stereodifferentiation Leads to Very High Purity

Discussions

• 🔓 #OpenAccess research by Markus Tost and Uli Kazmaier from Saarland University 👉Synthesis of oxylipids via a boronic ester cycloetherification approach #Chemsky #Organic #OCF_research doi.org/10 [bsky, 1 points, 0 comments]

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