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The synthesis of 2′-homouridine, its incorporation into a dinucleoside monophosphate and hydrolytic behaviour of the dimer

✍ Scribed by John B.J. Pavey; Anthony J. Lawrence; Andrew J. Potter; Richard Cosstick; Ian A. O'Neil


Publisher
Elsevier Science
Year
1998
Tongue
French
Weight
273 KB
Volume
39
Category
Article
ISSN
0040-4039

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✦ Synopsis


An efficient route to 2'-homouridine (1), a new nucleoside analogue, is reported that is based on an ene reaction. This nucleoside has been incorporated into a dinucleoside monophosphate and hydrolytic studies on the dimer show that it does not behave like a ribonucleotide.


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