803732-70-9Relevant articles and documents
Metal-free annulative hydrosulfonation of propiolate esters: synthesis of 4-sulfonates of coumarins and butenolides
Fernandes, Rodney A.,Gangani, Ashvin J.,Kunkalkar, Rupesh A.
, p. 3970 - 3984 (2020)
An efficient metal-free and cost-effective method for the synthesis of coumarin and butenolide 4-sulfonates (46 examples) has been developed. The reaction involves addition of sulfonic acids to ethyl propiolates followed by lactonization, resulting in direct formation of coumarin and butenolide 4-sulfonates. This methodology has been elaborated to Sonogashira and Suzuki coupling including the synthesis of rac-tolterodine.
A short, novel approach to 2,3,4a,5-tetrahydro-1H-pyrazino[1,2-a] quinoline-4,6-diones
Bernotas, Ronald C.
, p. 2165 - 2166 (2007/10/03)
An expeditious route to constrained arylpiperazinones has been developed. The key reaction formed the tricyclic system in one-pot via a 1,4-addition-lactamization-aromatic substitution sequence. Four examples were prepared.