One pot synthesis of chrysanthemic esters analogs

M.J. Devos, A. Krief

Research output: Contribution to journalArticle

Abstract

Chrysanthemic esters analogues diversely substituted on the cyclopropane ring and on the carbon-carbon double bond can be conveniently prepared in one pot from methyl 4-oxobutenoate by delayed addition of two differently substituted phosphorus ylides.
Original languageEnglish
Pages (from-to)1515-1518
Number of pages4
JournalTetrahedron Letters
Volume20
Issue number17
Publication statusPublished - 1 Jan 1979

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Esters
Carbon
Phosphorus
cyclopropane

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Devos, M.J. ; Krief, A. / One pot synthesis of chrysanthemic esters analogs. In: Tetrahedron Letters. 1979 ; Vol. 20, No. 17. pp. 1515-1518.
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Devos, MJ & Krief, A 1979, 'One pot synthesis of chrysanthemic esters analogs', Tetrahedron Letters, vol. 20, no. 17, pp. 1515-1518.

One pot synthesis of chrysanthemic esters analogs. / Devos, M.J.; Krief, A.

In: Tetrahedron Letters, Vol. 20, No. 17, 01.01.1979, p. 1515-1518.

Research output: Contribution to journalArticle

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