Storr, T.E., Strohmeier, J.A., Baumann, C.G. orcid.org/0000-0002-8818-972X et al. (1 more author) (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
Abstract
Novel rigid 8-biaryl-2'-deoxyadenosines with tuneable fluorescent properties can be accessed by an efficient sequential catalytic Pd-0-coupling approach.
Metadata
Authors/Creators: |
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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 |
Dates: |
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Institution: | The University of York |
Academic Units: | The University of York > Faculty of Sciences (York) > Chemistry (York) The University of York > Faculty of Sciences (York) > Biology (York) |
Depositing User: | Repository Administrator York |
Date Deposited: | 13 Oct 2010 14:54 |
Last Modified: | 06 Dec 2023 10:38 |
Published Version: | https://doi.org/10.1039/c0cc02043e |
Status: | Published |
Refereed: | Yes |
Identification Number: | https://doi.org/10.1039/c0cc02043e |
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