(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.
Download full-text PDF |
Source |
|---|---|
| http://dx.doi.org/10.1039/b808695h | DOI Listing |
Publication Analysis
Top Keywords
1s-cis-chrysanthemic acid
8
selected regiocontrolled
4
regiocontrolled transformations
4
transformations applied
4
applied synthesis
4
synthesis 1s-cis-chrysanthemic
4
acid 1s-34-epoxy-2255-tetramethylcyclohexanol
4
1s-34-epoxy-2255-tetramethylcyclohexanol 1s-cis-chrysanthemic
4
acid prepared
4
prepared steps
4
Similar Publications
Selected regiocontrolled transformations applied to the synthesis of (1S)-cis-chrysanthemic acid from (1S)-3,4-epoxy-2,2,5,5-tetramethylcyclohexanol.
Chem Commun (Camb)
October 2008
Laboratoire de Chimie Organique de Synthèse, Facultés Universitaires N.-D. de la Paix, 61 rue de Bruxelles, 5000, Namur, Belgium.
(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.
View Article and Find Full Text PDFWant AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!