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

Full text not available from this repository. (Request a copy)

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
UEA Research Groups:	Faculty of Science > Research Groups > Chemistry of Materials and Catalysis
Depositing User:	Pure Connector
Date Deposited:	13 Jan 2017 00:06
Last Modified:	05 May 2024 01:14
URI:	https://ueaeprints.uea.ac.uk/id/eprint/62043
DOI:	10.1039/c0cc02043e

Actions (login required)

View Item