A simple and rapid procedure for the synthesis of AMP"0, AMP'sO, and the corresponding guanosine derivatives is described. The method is based on the intermediate production of P"OC13 or P'\*OClj from PCIs, but does not involve their isolation, so that all steps involved can be carried out in the sa
✦ LIBER ✦
NMR study of the synthesis of 17O-enriched acetic acid by hydrolysis of acetic anhydride with 17O-enriched water
✍ Scribed by Heidi M. Hultman; Kristina Djanashvili; Joop A. Peters
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 127 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.1266
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✦ Synopsis
Abstract
^17^O‐enriched acetic acid (2.5% in ^17^O) was synthesized by hydrolysis of acetic anhydride with ^17^O‐enriched water. The reaction was monitored by ^17^O and ^1^H NMR spectroscopy. Acetic anhydride, ^17^O‐enriched in both the ether and the carbonyl oxygens, was observed as an intermediate. This can be ascribed to competition between acetic acid and water for nucleophilic attack on acetic anhydride. Copyright © 2003 John Wiley & Sons, Ltd.
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