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Issue 35, 2010
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A sequential direct arylation/Suzuki–Miyaura cross-coupling transformation of unprotected 2′-deoxyadenosine affords a novel class of fluorescent analogues

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Abstract

Novel rigid 8-biaryl-2′-deoxyadenosines with tuneable fluorescent properties can be accessed by an efficient sequential catalytic Pd0-coupling approach.

Graphical abstract: A sequential direct arylation/Suzuki–Miyaura cross-coupling transformation of unprotected 2′-deoxyadenosine affords a novel class of fluorescent analogues

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Publication details

The article was received on 23 Jun 2010, accepted on 22 Jul 2010 and first published on 17 Aug 2010


Article type: Communication
DOI: 10.1039/C0CC02043E
Citation: Chem. Commun., 2010,46, 6470-6472
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    A sequential direct arylation/Suzuki–Miyaura cross-coupling transformation of unprotected 2′-deoxyadenosine affords a novel class of fluorescent analogues

    T. E. Storr, J. A. Strohmeier, C. G. Baumann and I. J. S. Fairlamb, Chem. Commun., 2010, 46, 6470
    DOI: 10.1039/C0CC02043E

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