1426563-34-9Relevant academic research and scientific papers
Simple and rapid procedures for the synthesis of 5-acylated 4β-acylamido-and 4β-acetoxyneuraminic acid glycals
Agnolin, Irene S.,Rota, Paola,Allevi, Pietro,Gregorio, Antonio,Anastasia, Mario
, p. 6537 - 6547 (2013/01/15)
Two simple and rapid procedures affording 4β-acylamido-and 4β-acetoxyneuraminic acid glycals acylated or perfluoroacylated at the 5-amino group are reported. The first protocol avoids the formation of oxazolines to synthesize the 4β-acetamido glycals through the Ritter reaction. The second passes through the oxazoline derivative to prepare 4β-acetoxyneuraminic acid glycals. Both protocols start from peracetylated methyl neuraminate, acylated at the amino group with a normal, a glycolyl, or a perfluoroacyl group, or with the corresponding peracetylated glycal methyl esters (of the DANA or FANA series).
