799798-66-6Relevant academic research and scientific papers
Rearrangement of oxazolo[3,2-a]pyridines as an approach of synthesizing aza[3.3.2]cyclazines
Babaev, Eugene V.,Nevskaya, Aleksandra A.,Dlynnikh, Ilya V.
, p. 269 - 274 (2015)
[MediaObject not available: see fulltext.]5-Methyloxazolo[3,2-a]pyridinium salts were shown to react with (methylamino)acetaldehyde dimethyl acetal leading to the formation of functionalized 5-aminoindolizines, which in turn are capable of closing the pyr
Cathylation of 4,6-dimethyl-2-oxopyridine-3-carbonitrile derivatives leading to the synthesis of furo[2,3-b;4,5-b']dipyridines and novel tricyclic furo[2,3,4-ij][2,7]naphthyridine
Lin, Chyun-Feng,Lin, Yi-Feng,Lo, Yan-Chung,Chen, Kuo-Tung,Su, Tsann-Long
, p. 15 - 26 (2007/10/03)
Cathylation of ethyl 2-(3-cyano-4,6-dimethylpyridine-2-yloxy)acetate afforded a trace amount of new tricyclic furo[2,3,4-ij][2,7]naphthyridine derivative. An attempt was made for an alternate method for the synthesis this new tricyclic ring system. Treatm
