An advantageous synthesis of 5,6,7,8-tetra-hydrotetrazolo[1,5- a]pyridines

Article abstract of DOI:10.1080/00397919908085802

The one-step synthesis of various O-benzyl-protected glyconotetrazoles from the corresponding glyconolactams is reported. The method is superior to the previously employed cycloaddition of azidonitriles as it uses readily available starting materials and leads to higher yields.

Full text of DOI:10.1080/00397919908085802

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Synthetic Communications: An
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An Advantageous
Synthesis of 5,6,7,8-Tetra-
Hydrotetrazolo[1,5-a]Pyridines
Stefan Vonhoff a & Andrea Vasella a
a Laboratorium für Organische Chemie, ETH-
Zentrum , Universitätstrasse 16, CH-8092, Zurich,
Switzerland
Published online: 17 Sep 2007.
To cite this article: Stefan Vonhoff & Andrea Vasella (1999) An Advantageous
Synthesis of 5,6,7,8-Tetra-Hydrotetrazolo[1,5-a]Pyridines, Synthetic Communications:
An International Journal for Rapid Communication of Synthetic Organic Chemistry,
29:4, 551-560, DOI: 10.1080/00397919908085802
To link to this article: http://dx.doi.org/10.1080/00397919908085802
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