Convenient new synthesis of snoutene [1] utilizing a dipolar cycloaddition of 4-phenyl-1, 2, 4-triazolin-3, 5-dione
I Erden, A de Meijere
Index: Erden, Ishan; Meijere, Armin de Tetrahedron Letters, 1980 , vol. 21, p. 1837 - 1840
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Citation Number: 5
Abstract
Abstract 4-Phenyl-1, 2, 4-triazolin-3, 5-dione readily cycloadds to Nenitzescu's hydrocarbon 1 [6] with skeletal rearrangement. The major adduct 6 can conveniently be transformed to the azo compound 8, which upon photolysis or thermolysis yields up to 80% pentacyclo [3.3.
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