Synthesis of biurets via TMSNCO addition to 1-aminosugars: application in the de novo synthesis of dC oxidation products

We report an efficient one-step transformation of amines to biurets that has been applied to a number of 1-aminosugars and has led to thede novo synthesis of dfBU and dpBU, two known oxidatively produced lesions of 2 ′-deoxycytidine. To cite this article before page numbers are assigned, use the DOI form of citation above. The content of this RSS Feed (c) The Royal Society of Chemistry
Source: RSC - Organic and Biomolecular Chemistry - Category: Molecular Biology Authors: Source Type: research