666215-58-3Relevant academic research and scientific papers
Useful synthesis of the main central 2,3,6-trisubstituted pyridine skeleton of various thiostrepton-type macrocyclic antibiotics
Shin, Chung-Gi,Saito, Hirofumi,Yonezawa, Yasuchika
, p. 45 - 50 (2007/10/03)
A useful synthetic method for the main central 2-(2-oxazol-4-yl)-3-(4-thiazol-2-yl)-6-carboxypyridine skeleton [Fragment A] constructing various thiostrepton-type macrocyclic antibiotics is described, in which the precursor of Fragment A was derived from the authentic ethyl 2-(6-dimethoxymethyl-2-trifluoromethanesulfonyloxy-3-pyridyl) thiazole-4-carboxylate in 14 steps. Finally, the fragment condensation of Fragment A with the already prepared carboxy component dipeptide [Fragment B] proceeded first to give the precursor of Fragment A-B.
