前往化源商城

Tetrahedron Letters

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

文献索引:Erden, Ishan; Meijere, Armin de Tetrahedron Letters, 1980 , vol. 21, p. 1837 - 1840

全文:HTML全文

被引用次数: 5

摘要

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.