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

Storr, Thomas E., Strohmeier, Johanna A., Baumann, Christoph G. and Fairlamb, Ian J. S. (2010) A sequential direct arylation/Suzuki–Miyaura cross-coupling transformation of unprotected 2′-deoxyadenosine affords a novel class of fluorescent analogues. Chemical Communications, 46 (35). pp. 6470-6472. ISSN 1359-7345

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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.

Item Type: Article
Faculty \ School: Faculty of Science > School of Chemistry
Depositing User: Pure Connector
Date Deposited: 13 Jan 2017 00:06
Last Modified: 22 Apr 2020 02:26
URI: https://ueaeprints.uea.ac.uk/id/eprint/62043
DOI: 10.1039/c0cc02043e

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