Synthesis 2014; 46(24): 3315-3318
DOI: 10.1055/s-0034-1378497
paper
© Georg Thieme Verlag Stuttgart · New York

Synthesis of Functional Tripodal Thioacetates

Florian Kretschmer
a  Laboratory of Organic and Macromolecular Chemistry (IOMC), Friedrich Schiller University Jena, Humboldtstr. 10, 07743 Jena, Germany
b  Jena Center for Soft Matter (JCSM), Friedrich Schiller University Jena, Philosophenweg 7, 07743 Jena, Germany   Fax: +49(3641)948202   eMail: ulrich.schubert@uni-jena.de
,
Martin D. Hager
a  Laboratory of Organic and Macromolecular Chemistry (IOMC), Friedrich Schiller University Jena, Humboldtstr. 10, 07743 Jena, Germany
b  Jena Center for Soft Matter (JCSM), Friedrich Schiller University Jena, Philosophenweg 7, 07743 Jena, Germany   Fax: +49(3641)948202   eMail: ulrich.schubert@uni-jena.de
,
Ulrich S. Schubert*
a  Laboratory of Organic and Macromolecular Chemistry (IOMC), Friedrich Schiller University Jena, Humboldtstr. 10, 07743 Jena, Germany
b  Jena Center for Soft Matter (JCSM), Friedrich Schiller University Jena, Philosophenweg 7, 07743 Jena, Germany   Fax: +49(3641)948202   eMail: ulrich.schubert@uni-jena.de
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Publikationsverlauf

Received: 12. Mai 2014

Accepted after revision: 17. Juni 2014

Publikationsdatum:
15. September 2014 (online)


Abstract

A versatile route for the synthesis of tripodal thioacetates is reported. Based on the esterification of commercial pentaerythritol tribromide, the method enables the easy introduction of different functional moieties, e.g., into self-assembled monolayers.

Supporting Information

 
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