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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
RESUMEN

[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.

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Sigma-Aldrich
Allyltrimethylsilane, 98%