Selected regiocontrolled transformations applied to the synthesis of (1S)-cis-chrysanthemic acid from (1S)-3,4-epoxy-2,2,5,5-tetramethylcyclohexanol

A. Krief; H.Y. Gondal; A. Kremer

doi:10.1039/b808695h

Selected regiocontrolled transformations applied to the synthesis of (1S)-cis-chrysanthemic acid from (1S)-3,4-epoxy-2,2,5,5-tetramethylcyclohexanol

A. Krief, H.Y. Gondal, A. Kremer

Unite de recherche en chimie organique

Résultats de recherche: Contribution à un journal/une revue › Article › Revue par des pairs

Résumé

(1S)-cis-Chrysanthemic acid has been prepared in a few steps with complete control of the relative and absolute stereochemistry using regiocontrolled epoxide ring opening, diol mono-oxidation and cyclopropanation. © The Royal Society of Chemistry.

langue originale	Anglais
Pages (de - à)	4753-4755
Nombre de pages	3
journal	Chemical Communications
Numéro de publication	39
Les DOIs	https://doi.org/10.1039/b808695h
Etat de la publication	Publié - 21 oct. 2008

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10.1039/b808695h

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title = "Selected regiocontrolled transformations applied to the synthesis of (1S)-cis-chrysanthemic acid from (1S)-3,4-epoxy-2,2,5,5-tetramethylcyclohexanol",

abstract = "(1S)-cis-Chrysanthemic acid has been prepared in a few steps with complete control of the relative and absolute stereochemistry using regiocontrolled epoxide ring opening, diol mono-oxidation and cyclopropanation. {\textcopyright} The Royal Society of Chemistry.",

keywords = "Cyclohexanols, Epoxy Compounds, Molecular Structure, Pyrethrins, Stereoisomerism",

author = "A. Krief and H.Y. Gondal and A. Kremer",

year = "2008",

month = oct,

day = "21",

doi = "10.1039/b808695h",

language = "English",

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journal = "Chemical Communications",

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T1 - Selected regiocontrolled transformations applied to the synthesis of (1S)-cis-chrysanthemic acid from (1S)-3,4-epoxy-2,2,5,5-tetramethylcyclohexanol

AU - Krief, A.

AU - Gondal, H.Y.

AU - Kremer, A.

PY - 2008/10/21

Y1 - 2008/10/21

N2 - (1S)-cis-Chrysanthemic acid has been prepared in a few steps with complete control of the relative and absolute stereochemistry using regiocontrolled epoxide ring opening, diol mono-oxidation and cyclopropanation. © The Royal Society of Chemistry.

AB - (1S)-cis-Chrysanthemic acid has been prepared in a few steps with complete control of the relative and absolute stereochemistry using regiocontrolled epoxide ring opening, diol mono-oxidation and cyclopropanation. © The Royal Society of Chemistry.

KW - Cyclohexanols

KW - Epoxy Compounds

KW - Molecular Structure

KW - Pyrethrins

KW - Stereoisomerism

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U2 - 10.1039/b808695h

DO - 10.1039/b808695h

M3 - Article

C2 - 18830482

SN - 1359-7345

SP - 4753

EP - 4755

JO - Chemical Communications

JF - Chemical Communications

IS - 39

ER -

Selected regiocontrolled transformations applied to the synthesis of (1S)-cis-chrysanthemic acid from (1S)-3,4-epoxy-2,2,5,5-tetramethylcyclohexanol

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