(4-Chloro-7H-pyrrolo[2,3-d]pyr

Synthesis and Properties of 7‐Substituted 7‐Deazapurine (Pyrrolo[2,3‐d]pyrimidine) 2′‐Deoxyribonucleosides

‐1) 4‐Chloro‐5‐iodo‐7H ‐pyrrolo[2,3‐d ]pyrimidine ( S.7 ; see Pudlo et al., ) 2‐Deoxy‐3,5‐di‐O ‐(p ‐toluoyl)‐α‐D‐erythro ‐pentofuranosyl chloride ( S.8 ; see Hoffer

Convenient and Efficient Approach to the Permanent or Reversible Conjugation of RNA and DNA Sequences with Functional Groups

Figure 4.52.1 Synthesis of 2′‐ O ‐(aminooxymethyl)ribonucleosides (S.5 a‐d ). Abbreviations: BP , a uracil‐1‐yl, b N 4 ‐benzoylctytosin‐1‐yl, c N 6 ‐isobutyryladenin‐9‐yl, d N 2 ‐phenoxyacetylguanin‐9‐yl; DBU, 1,8‐diazabicyclo[5.4.0]undec‐7‐ene; B

Biotinylation of a Propargylated Cyclic (3′‐5′) Diguanylic Acid and of Its Mono‐6‐Thioated Analog Under “Click” Conditions

. Opin. Immunol. 23:10‐20.    Berndl, S., Herzig, N., Kele, P., Lachmann, D., Li, X., Wolfbeis, O.S., and Wagenknecht, H.‐A. 2009. Comparison of a nucleosidic vs non‐nucleosidic