The Synthesis of Fluorescent DNA Intercalator Precursors through Efficient Multiple Heck Reactions
Nigel A. Lengkeek A , Ramiz A. Boulos A , Allan J. McKinley A , Thomas V. Riley C , Boris Martinac B and Scott G. Stewart A DA M313, Chemistry, School of Biomedical, Biomolecular and Chemical Science, University of Western Australia, 35 Stirling Highway, Crawley, WA, 6009, Australia.
B Victor Chang Cardiac Research Institute, Lowy Packer Building, 405 Liverpool Street, Darlinghurst, Sydney, NSW 2010, Australia.
C M502, Microbiology and Immunology, School of Biomedical, Biomolecular and Chemical Sciences, The University of Western Australia, 35 Stirling Hwy, Nedlands, WA 6009, Australia.
D Corresponding author. Email: sgs@cyllene.uwa.edu.au
Australian Journal of Chemistry 64(3) 316-323 https://doi.org/10.1071/CH10374
Submitted: 21 October 2010 Accepted: 10 January 2011 Published: 11 March 2011
Abstract
A highly efficient synthesis of p-carboethoxy-tristyryl and carboethoxy-terastyrenyl benzene derivatives through a multiple Heck cross coupling reaction is reported. This reaction provides an efficient route to DNA intercalator precursors containing a benzene core.
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