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Updated: Jul 9, 2026

Synthesis and Bioconjugation of Thiol-Reactive Reagents for the Creation of Site-Selectively Modified Immunoconjugates
Published on: March 6, 2019
Efficient synthesis of thymidine boranophosphoramidates conjugated with amino acids
Shoeb I Khan1, Barbara Ramsay Shaw
1Department of Chemistry, Duke University, Durham, North Carolina 27708, USA. brshaw@chem.duke.edu
Abstract:
An efficient synthesis of a thymidine boranophosphoramidate prodrug was accomplished using a phosphoramidite approach in high yield. This new class of compounds is designed to have improved antiviral and anticancer advantages conferred by combining the boranophosphate and normal nucleoside amino acid phosphoramidate. Compounds were characterized by MS and 31P NMR.
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