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

By T.E. Storr, J.A. Strohmeier, C.G. Baumann and I.J.S. Fairlamb

Abstract

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

Topics: 2506, 2505, 2508, 2504, 2503, 1503, 1600
Year: 2010
DOI identifier: 10.1039/c0cc02043e
OAI identifier: oai:eprints.whiterose.ac.uk:19794

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