Andreas Marx,Peter Erdmann,Martin Senn,Steffi K. Koerner,Tobias Jungo,Mario Petretta,Petra Imwinkelried,Adrian Dussy,Klaus J. Kulicke,Ludwig Macko,Margareta Zehnder,Bernd Giese
Abstract Two synthetic pathways towards 4′‐C‐acylthymidines are presented. These modified mononucleosides are precursors of the 2′‐deoxyribonucleotide 4′‐C‐radical. They were converted into their corresponding 3′‐O‐[(2‐cyanoethyl) N,N‐diisopropylphosphoramidites] 3a–c and incorporated in oligonucleotides by solid‐phase synthesis. The structure of some modified nucleosides was revealed by X‐ray crystal‐structure analysis.