Highly Stereoselective Synthesis of 1,6-Ketoesters Mediated by Ionic Liquids: A Three-component Reaction Enabling Rapid Access to a New Class of Low Molecular Weight Gelators

Henrik Sund&#233;n; Linda Ta; Anton Axelsson

doi:10.3791/53213

/

Sintesi altamente stereoselettiva di 1,6-chetoesteri Mediata da liquidi ionici: una reazione a tre componenti Abilitazione accesso rapido a una nuova classe di basso peso molecolare Gelators

JoVE Journal
Chimica

È necessario avere un abbonamento a JoVE per visualizzare questo. Accedi o inizia la tua prova gratuita.

JoVE Journal Chimica

Highly Stereoselective Synthesis of 1,6-Ketoesters Mediated by Ionic Liquids: A Three-component Reaction Enabling Rapid Access to a New Class of Low Molecular Weight Gelators

Sintesi altamente stereoselettiva di 1,6-chetoesteri Mediata da liquidi ionici: una reazione a tre componenti Abilitazione accesso rapido a una nuova classe di basso peso molecolare Gelators

Please note that all translations are automatically generated. Click here for the English version.

8,655 Views

•

06:31 min

•

November 27, 2015

DOI:

10.3791/53213-v

DOI:

10.3791/53213-v

•

06:31 min

November 27, 2015

•

1 Views

Henrik Sundén¹, Linda Ta¹, Anton Axelsson¹

¹Chemistry and Chemical Engineering,Chalmers University of Technology

Summary

Ionic liquids (ILs) mediate fast, simple and cheap access to 1,6-ketoesters in high diastereoselectivities and good yields. The reaction protocol is robust and the 1,6-ketoesters can be obtained in gram scale after a simple filtration protocol. Moreover, the 1,6-ketoesters are potent gelators in hydrocarbon solvents.