Synthesis of isoindole derivatives by palladium-catalyzed domino reaction of (2-alkynyl)phenylketone o-pentafluorobenzoyloximes
Isoindole derivatives were synthesized by the palladium-catalyzed cyclization of (2-alkynyl)phenylketone O-pentafluoro-benzoyloximes in the presence of organometallic compounds such as sodium formate and aryl boronic acid. Georg Thieme Verlag Stuttgart - New York.
Kitamura, Mitsuru,Moriyasu, Yohei,Okauchi, Tatsuo
p. 643 - 646
(2011/05/02)
Iminyls. Part 9. Intramolecular Addition of an Iminyl to an Alkene
Phenyl o-styrylphenyl iminyl, generated by oxidation of the corresponding O-carboxymethyloxime with persulphate and by thermolysis of the perester of that acid, cyclises to give a mixture of isoquinoline and 1H-isoindole derivatives.The intermediate radicals have been investigated by e.s.r.
Atmaram, Shiravante,Forrester, Alexander R.,Gill, Melvin,Thomson, Ronald H.
p. 1721 - 1724
(2007/10/02)
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