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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 1997 Volume 7, Issue 4, Pages 141–143 (Mi mendc4825)

This article is cited in 7 papers

Synthesis of diethyl oxo phosphonates from monoterpene ketones – carvone, pinocarvone and 2-caren-4-one

V. D. Kolesnika, M. M. Shakirovb, A. V. Tkachevb

a Department of Natural Sciences, Novosibirsk State University, Novosibirsk, Russian Federation
b N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation

Abstract: Reaction of α,β-unsaturated monoterpenic ketones – carvone, pinocarvone and 2-caren-4-one – with the sodium salt of diethylphosphite in diethylphosphite media results in regioselective addition to the conjugated carbon–carbon double bond and formation of the corresponding oxophosphonates.

Language: English

DOI: 10.1070/MC1997v007n04ABEH000764



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