Synthesis of inhibitors of adenosine deaminase. A total synthesis of erythro-3-(adenin-9-yl)-2-nonanol and its isomers from chiral precursors

DC Baker, LD Hawkins

Index: Baker, David C.; Hawkins, L. D. Journal of Organic Chemistry, 1982 , vol. 47, # 11 p. 2179 - 2184

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Citation Number: 25

Abstract

Baker and Hawkins nificantly alter the [" ID values, indicating that these molecules are indeed resistant to base-promoted racemization, at least in the hydrated state. Attempts to examine the enantiomeric aldehydes in the presence of the chiral shift reagent tris [3- [(trifluoromethy1) hydroxy-methylene)]-(+)-camphorato] europuim (III) failed to resolve any racemic compounds. While the experiment was not conclusive, one could observe signals ...