Nucleocyclitols. Synthesis of ethanolamino-purinyl inositol derivatives and their reaction with thionyl chloride

Article abstract of DOI:10.1080/15257779408013206

The reaction of mono- and diethanolamine with a 6-chloropurinyl inositol gave 6-ethanolaminopurinyl-inositol derivatives which by reaction with thionyl chloride generated, through quaternization of N¹ of the purine, condensed imidazo-purinyl ca

Full text of DOI:10.1080/15257779408013206

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Nucleosides and Nucleotides
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Nucleocyclitols. Synthests of
Ethanolamino-Purinyl Inositol Derivatives
and Their Reaction With Thionyl
Chloride
S. R. Leicach a , M. E. Gelpi a & R. A. Cadenas a
a Departarnento de Quimica. Facultad de Agronomia , Universidad
de Buenos Aires , (1417) Av. San Martin, 4453., Buenos Aires,
Argentina
Published online: 24 Sep 2006.
To cite this article: S. R. Leicach , M. E. Gelpi & R. A. Cadenas (1994) Nucleocyclitols. Synthests of
Ethanolamino-Purinyl Inositol Derivatives and Their Reaction With Thionyl Chloride, Nucleosides and
Nucleotides, 13:10, 2051-2058, DOI: 10.1080/15257779408013206
To link to this article: http://dx.doi.org/10.1080/15257779408013206
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