203632-34-2Relevant academic research and scientific papers
Synthesis of orotidine by intramolecular nucleosidation
Kim,Krishnamurthy
supporting information, p. 5618 - 5621 (2015/03/30)
An intramolecular nucleosidation approach provides easy access to orotidine in high yields. Notably, orotate itself is used as a leaving group at the anomeric position. This method has the potential for facile access to derivatives of orotidine of therapeutic interest, with implications for prebiotic formation of nucleosides. This journal is
One-pot synthesis of acyclic nucleosides from carbohydrate derivatives, by combination of tandem and sequential reactions
Boto, Alicia,Hernandez, Dacil,Hernandez, Rosendo,Alvarez, Eleuterio
, p. 9523 - 9532 (2008/03/28)
(Chemical Equation Presented) The design of processes which combine tandem and sequential reactions allows the transformation of readily available precursors into high-profit products. This strategy is illustrated by the one-pot synthesis of acyclic nucle
