By the same authors

From the same journal

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

Research output: Contribution to journalArticle

Full text download(s)

Links

Published copy (DOI)

Author(s)

Department/unit(s)

Publication details

JournalChemical Communications
DatePublished - 21 Sep 2010
Issue number35
Volume46
Number of pages3
Pages (from-to)6470-6472
Original languageEnglish

Abstract

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

Bibliographical note

© 2010 Royal Society of Chemistry. This is an author produced version of a paper published in Chemical Communications. Uploaded in accordance with the publisher's self archiving policy.

    Research areas

  • NUCLEOSIDE TRIPHOSPHATES, POLYMERASE INCORPORATION, OLIGONUCLEOTIDE PROBES, BASE ANALOGS, DNA, PURINE, 2'-DEOXYURIDINE, CONSTRUCTION, DERIVATIVES, GUANOSINE

Discover related content

Find related publications, people, projects, datasets and more using interactive charts.

View graph of relations