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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. (orcid.org/0000-0002-8818-972X) and Fairlamb, I.J.S. (orcid.org/0000-0002-7555-2761) (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 1364-548X

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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: 22 Mar 2016 00:02
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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