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Synthesis of 1,2-dioxolanes by annulation reactions of peroxycarbenium ions with alkenes.

Organic letters (2005-10-08)
Armando Ramirez, K A Woerpel
ZUSAMMENFASSUNG

[reaction: see text] The annulation reactions of alkenes with peroxycarbenium ions enable the synthesis of a variety of functionalizable 1,2-dioxolanes. Triethysilyl-protected peroxycarbenium ions proved to be optimal for the annulation reaction. Using this method, plakinic acid analogues can be synthesized in three steps from the corresponding ketone and alkene.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
Allyltrimethylsilan, 98%