Synthesis 2012; 44(14): 2249-2254
DOI: 10.1055/s-0031-1290444
paper
© Georg Thieme Verlag Stuttgart · New York

Tri- and Tetravalent Photoactivable Cross-Linking Agents

Alexandre Welle
Université catholique de Louvain, Institute of Condensed matter and Nanosciences – IMCN / MOST, Bâtiment Lavoisier, place Louis Pasteur L4.01.02, 1348 Louvain-la-Neuve, Belgium, Fax: +32(10)474168   Email: jacqueline.marchand@uclouvain.be
,
François Billard
Université catholique de Louvain, Institute of Condensed matter and Nanosciences – IMCN / MOST, Bâtiment Lavoisier, place Louis Pasteur L4.01.02, 1348 Louvain-la-Neuve, Belgium, Fax: +32(10)474168   Email: jacqueline.marchand@uclouvain.be
,
Jacqueline Marchand-Brynaert*
Université catholique de Louvain, Institute of Condensed matter and Nanosciences – IMCN / MOST, Bâtiment Lavoisier, place Louis Pasteur L4.01.02, 1348 Louvain-la-Neuve, Belgium, Fax: +32(10)474168   Email: jacqueline.marchand@uclouvain.be
› Author Affiliations
Further Information

Publication History

Received: 28 February 2012

Accepted after revision: 08 May 2012

Publication Date:
18 June 2012 (online)


Abstract

A modular synthesis of photoactivable cross-linking agents is described, using an aromatic core, di- or triethyleneglycol spacers and photoaffinity labeling synthons that feature either perfluorophenyl azide or aryl(trifluoromethyl)diazirine motifs. Symmetrical and nonsymmetrical trivalent structures were obtained from phloroglucinol and dopamine, respectively. Symmetrical tetravalent structures resulted from the coupling of two dopamine derivatives with oxalyl chloride.

Supporting Information

 
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