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Updated: Feb 27, 2026

Chemoselective Modification of Viral Surfaces via Bioorthogonal Click Chemistry
Published on: August 19, 2012
A novel application of the Staudinger ligation to access neutral cyclic di-nucleotide analog precursors via a
M H Fletcher1, C E Burns-Lynch1, K W Knouse1
1Department of Chemistry, Temple University, Philadelphia, PA 19122, USA.
Abstract:
Our efforts to develop a scalable and divergent synthesis of cyclic di-nucleotide analog precursors have resulted in (1) an orthogonally protected di-amino carbohydrate as well as (2) the novel application of the Staudinger ligation to provide medium-sized macrocycles featuring carbamate or urea linkages.
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