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An improved procedure is described for the efficient and high-yield (76-91%) synthesis of nucleoside diphosphate sugars from the readily available nucleoside 5'-monophosphomorpholidate and sugar 1-phosphate in the presence of 1H-tetrazole. Comparative kinetic investigations by means of (31)P NMR spectroscopy with different additives (1,2,4-triazole, acetic acid, N-hydroxysuccinimide, 4-(dimethylamino)pyridine hydrochloride, perchloric acid) and mass spectrometric analysis suggest that tetrazole acts as an acid and as a nucleophilic catalyst in the pyrophosphate bond formation.
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Valentin Wittmann
University of Konstanz
Chi‐Huey Wong
Brigham Young University
The Journal of Organic Chemistry
Scripps Research Institute
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Wittmann et al. (Tue,) studied this question.
synapsesocial.com/papers/6a130cf106ed52b5c2c0fd71 — DOI: https://doi.org/10.1021/jo9620066