Novel synthesis of (d,l) trans-chrysanthemic acid involving a β-diketone fragmentation

A. Krief; S. Jeanmart

doi:10.1016/S0040-4039(02)01270-4

Novel synthesis of (d,l) trans-chrysanthemic acid involving a β-diketone fragmentation

A. Krief, S. Jeanmart

Unit of organic chemistry

Research output: Contribution to journal › Article › peer-review

Abstract

Methyl (d,l) trans-chrysanthemate as well as its cis-diastereoisomer have been prepared from dimethyl dimedone, one of their isomers, in a few steps and with complete control of the relative stereochemistry.

Original language	English
Pages (from-to)	6167-6168
Number of pages	2
Journal	Tetrahedron Letters
Volume	43
Issue number	35
DOIs	https://doi.org/10.1016/S0040-4039(02)01270-4
Publication status	Published - 26 Aug 2002

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title = "Novel synthesis of (d,l) trans-chrysanthemic acid involving a β-diketone fragmentation",

abstract = "Methyl (d,l) trans-chrysanthemate as well as its cis-diastereoisomer have been prepared from dimethyl dimedone, one of their isomers, in a few steps and with complete control of the relative stereochemistry.",

author = "A. Krief and S. Jeanmart",

year = "2002",

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doi = "10.1016/S0040-4039(02)01270-4",

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T1 - Novel synthesis of (d,l) trans-chrysanthemic acid involving a β-diketone fragmentation

AU - Krief, A.

AU - Jeanmart, S.

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Y1 - 2002/8/26

N2 - Methyl (d,l) trans-chrysanthemate as well as its cis-diastereoisomer have been prepared from dimethyl dimedone, one of their isomers, in a few steps and with complete control of the relative stereochemistry.

AB - Methyl (d,l) trans-chrysanthemate as well as its cis-diastereoisomer have been prepared from dimethyl dimedone, one of their isomers, in a few steps and with complete control of the relative stereochemistry.

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U2 - 10.1016/S0040-4039(02)01270-4

DO - 10.1016/S0040-4039(02)01270-4

M3 - Article

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JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 35

ER -

Novel synthesis of (d,l) trans-chrysanthemic acid involving a β-diketone fragmentation

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