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A sequential direct arylation/Suzuki-Miyaura cross-coupling transformation of unprotected 2 '-deoxyadenosine affords a novel class of fluorescent analogues

Storr, T.E., Strohmeier, J.A., Baumann, C.G. and Fairlamb, I.J.S. (2010) A sequential direct arylation/Suzuki-Miyaura cross-coupling transformation of unprotected 2 '-deoxyadenosine affords a novel class of fluorescent analogues. Chemical Communications. pp. 6470-6472. ISSN 1359-7345

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Abstract

Novel rigid 8-biaryl-2'-deoxyadenosines with tuneable fluorescent properties can be accessed by an efficient sequential catalytic Pd-0-coupling approach.

Item Type: Article
Copyright, Publisher and Additional Information: © 2010 Royal Society of Chemistry. This is an author produced version of a paper published in Chemical Communications. Uploaded in accordance with the publisher's self archiving policy.
Keywords: NUCLEOSIDE TRIPHOSPHATES, POLYMERASE INCORPORATION, OLIGONUCLEOTIDE PROBES, BASE ANALOGS, DNA, PURINE, 2'-DEOXYURIDINE, CONSTRUCTION, DERIVATIVES, GUANOSINE, Metals and Alloys, Materials Chemistry, Surfaces, Coatings and Films, Electronic, Optical and Magnetic Materials, Ceramics and Composites, Catalysis, Chemistry
Institution: The University of York
Academic Units: The University of York > Chemistry (York)
The University of York > Biology (York)
Depositing User: Repository Administrator York
Date Deposited: 13 Oct 2010 14:54
Last Modified: 31 Aug 2014 00:01
Published Version: http://dx.doi.org/10.1039/c0cc02043e
Status: Published
Refereed: Yes
Related URLs:
URI: http://eprints.whiterose.ac.uk/id/eprint/19794

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