2′-(三氟甲基)苯乙酮;17408-14-9;≥98%;S

Uridine 2′‐Carbamates: Facile Tools for Oligonucleotide 2′‐Functionalization

H‐Leu‐Phe‐NH 2 hydrochloride (for S.4f ) Triethylamine (TEA), ≥99% pure

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

systems are shown in the first two structures. Compounds: S.1 , 7‐deaza‐2′‐deoxyadenosine; S.2 , 7‐deaza‐2′‐deoxyguanosine; S.3 , 2‐amino‐7‐deaza‐2′‐deoxyadenosine; S.4 , 7‐deaza‐2′‐deoxyisoguanosine; S.5 , 7‐deaza‐2′‐deoxyinosine; S.6 , 7‐deaza‐2′

Two‐Step, One‐Pot Synthesis of Inosine, Guanosine, and 2′‐Deoxyguanosine O6‐Ethers via Intermediate O6‐(Benzotriazol‐1‐yl) Derivatives

) Guanosine ( S.5 ), 98% (Lancaster Synthesis) 2′‐Deoxyguanosine ( S.9 ), 98% (Transgenomic, http://www/transgenomic.com