The ''thio effect' on the hydrolysis and transesterification of ribonucleoside phosphoesters




Oivanen M, Ora M, Lonnberg H

PublisherINST ORGANIC CHEM AND BIOCHEM

1996

Collection of Czechoslovak Chemical Communications

COLLECTION OF CZECHOSLOVAK CHEMICAL COMMUNICATIONS

COLLECT CZECH CHEM C

61

S1

S4

4

0010-0765



The effects that replacing one of the non-bridging oxygens of ribonucleoside phosphoesters with sulfur exerts on the kinetics of phosphoester hydrolysis and intramolecular transesterification under various conditions are discussed. The experimental examples refer to the phosphoromonothioate analogs of uridylyl(3',5')uridine, uridine 2',3'-cyclic monophosphate, and uridine 2'- and 3'-monophosphates.



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