Mitsunobu reactions for the synthesis of carbocyclic analogues of nucleosides: Examintion of the regioselectivity

Article abstract of DOI:10.1080/00397919308011216

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 with a variety of alcohols were examined and found to depend upon both substituents of the bases and kind of the alcohols.

Full text of DOI:10.1080/00397919308011216

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Synthetic Communications: An
International Journal for Rapid
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Organic Chemistry
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Mitsunobu Reactions for the
Synthesis of Carbocyclic
Analogues of Nucleosides:
Examination of the
Regioselectivity1
Akemi Toyota a , Nobuya Katagiri a & Chikara Kaneko
a
a Pharmaceutical Institute, Tohoku University ,
Aobayama, Sendai, 980, Japan
Published online: 24 Sep 2006.
To cite this article: Akemi Toyota , Nobuya Katagiri & Chikara Kaneko (1993)
Mitsunobu Reactions for the Synthesis of Carbocyclic Analogues of Nucleosides:
Examination of the Regioselectivity1 , Synthetic Communications: An International
Journal for Rapid Communication of Synthetic Organic Chemistry, 23:9, 1295-1305,
DOI: 10.1080/00397919308011216
To link to this article: http://dx.doi.org/10.1080/00397919308011216
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