Tellurium-based organic synthesis: A novel one-pot formation of 2-oxazolines from alkenes induced by amidotellurinylation
Benzenetellurinyl trifluoroacetate readily reacts with alkenes in acetonitrile at 75°C to give 2-oxazolines in one pot.
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A facile preparation of various N-heterocycles using amides and olefins
2014, Tetrahedron LettersCitation Excerpt :Unfortunately very poor yields were also obtained with thiobenzamide and the preparation of 4e was not further pursued. The use of vinylanisole 2 and vinylpyridine 3 allowed for the formation of the known compounds 2a, 2e, 3a, 3b, 3d, 3e (Table 1, entries 2 and 3).16,17 The yields ranged from good to low, especially for compounds 2e, 3b, and 3d.
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1996, Comprehensive Heterocyclic Chemistry II: A Review of the Literature 1982-1995The chemistry of 2-oxazolines (1985-present)
1994, TetrahedronFive-Membered Ring Systems: With O and N Atoms
1990, Progress in Heterocyclic ChemistryTransformation of allylsilanes into allylamines via phenyltellurinylation
1988, Tetrahedron Letters
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