A sequential direct arylation/Suzuki–Miyaura cross-coupling transformation of unprotected 2′-deoxyadenosine affords a novel class of fluorescent analogues†
Johanna A. Strohmeier,Christoph G. Baumann,Ian J. S. Fairlamb
Chemical Communications Pub Date : 08/17/2010 00:00:00 , DOI:10.1039/C0CC02043E
Abstract
Novel rigid 8-biaryl-2′-deoxyadenosines with tuneable fluorescent properties can be accessed by an efficient sequential catalytic Pd0-coupling approach.
