Issue 35, 2010
From the journal:

Chemical Communications

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

Thomas E. Storr,ab   Johanna A. Strohmeier,b   Christoph G. Baumann*b  and  Ian J. S. Fairlamb*a  

* Corresponding authors

a Department of Chemistry, University of York, York, UK
E-mail: ijsf1@york.ac.uk

b Department of Biology, University of York, York, UK
E-mail: cb17@york.ac.uk

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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Article information

DOI
https://doi.org/10.1039/C0CC02043E
Article type
Communication
Submitted
23 Jun 2010
Accepted
22 Jul 2010
First published
17 Aug 2010

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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