An improved procedure for the synthesis of 1,3-dideazaadenosine

Article abstract of DOI:10.1080/00397919508011408

The preparation of the titled compound has been conveniently achieved in five steps, and in 43% overall yield. The large scale monoreduction of 2,6-dinitroaniline, and the stannic chloride catalyzed glycosylation of 4 to obtain 6 as the only product (86%) are two important reactions in this five step synthesis.

Full text of DOI:10.1080/00397919508011408

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Synthetic Communications:
An International Journal
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Synthetic Organic Chemistry
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An Improved Procedure
for the Synthesis of 1,3-
Dideazaadenosine
Theresa A. Devlin a & David J. Jebaratnam a
a Department of Chemistry , Northeastern
University , Boston, MA, 02115, USA
Published online: 23 Sep 2006.
To cite this article: Theresa A. Devlin & David J. Jebaratnam (1995) An Improved
Procedure for the Synthesis of 1,3-Dideazaadenosine, Synthetic Communications:
An International Journal for Rapid Communication of Synthetic Organic Chemistry,
25:5, 711-718, DOI: 10.1080/00397919508011408
To link to this article: http://dx.doi.org/10.1080/00397919508011408
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