Mitsunobu Reactions for the Synthesis of Carbocyclic Analogues of Nucleosides: Examination of the Regioselectivity1
- 1 May 1993
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 23 (9) , 1295-1305
- https://doi.org/10.1080/00397919308011216
Abstract
In order to provide a general synthetic method for carbocyclic nucleosides, regioselectivities in Mitsunobu reaction of purine, pyrimidin-2-one and their substituted derivatives with a variety of alcohols were examined and found to depend upon both substituents of the bases and kind of the alcohols.Keywords
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