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An improved method for [5′-2H]-labelling 3′-O-acetylthymidine

✍ Scribed by John Orban; Brian R. Reid


Publisher
John Wiley and Sons
Year
1989
Tongue
French
Weight
196 KB
Volume
27
Category
Article
ISSN
0022-2135

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✦ Synopsis


3'-0Acetylthymidine (I) was converted to the 0-acetoxy aldehyde (3) using a modified Swern oxidation procedure. The crude product was reduced with sodium borodeuteride to give, after chromatography, [5'-2H]-3'-CL-acety1thymidine (4) in 68% overall yield from -1. The extent of deuterium incorporation was >95% as judged by 'H NMR spectroscopy.


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