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. Author manuscript; available in PMC: 2014 Aug 22.
Published in final edited form as: RSC Adv. 2013 Aug 22;3(43):10.1039/C3RA42769B. doi: 10.1039/C3RA42769B

Table 1.

Reactants and products structures and yields of formation dinucleotide cap analogues.

Product (No) ελ260 (M−1cm−1) Nucleophile (No) Activated nucleotide (No) HPLC conv. [%] Yield a/b [%]
Ant-m7GpppG (1) 21700 Ant-m7GDP (6) GMP-Im (15) 92 39/34
Mant-m7GpppG (2) 26800 Mant-m7GDP (7) GMP-Im (15) 81 36/17
Mant-m7GppCH2pG (3) 26400 Mant-m7GMP (8) GpCH2p-Im (18) 63 36/12
Mant-m7GpCH2ppG (4) 24000 Mant-m7GpCH2p (9) GMP-Im (15) 72 23/8
Ant-m27,2′-OGpppG (5) 21600 Ant-m27,2′-OGMP (10) GDP-Im (17) 95 83/26
a

yield after ion exchange chromatography;

b

yield after additional RP HPLC purification