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

Thomas E. Storr, Johanna A. Strohmeier, Christoph G. Baumann, Ian J. S. Fairlamb

Research output: Contribution to journalArticlepeer-review

31 Citations (Scopus)


Novel rigid 8-biaryl-2′-deoxyadenosines with tuneable fluorescent properties can be accessed by an efficient sequential catalytic Pd0-coupling approach.
Original languageEnglish
Pages (from-to)6470-6472
Number of pages3
JournalChemical Communications
Issue number35
Early online date17 Aug 2010
Publication statusPublished - 21 Sep 2010

Cite this